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Relevant bibliographies by topics / Cell surface molecules][Morphogenesis

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Academic literature on the topic 'Cell surface molecules][Morphogenesis'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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Journal articles on the topic "Cell surface molecules][Morphogenesis"

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Niessen, Carien M., Deborah Leckband, and Alpha S. Yap. "Tissue Organization by Cadherin Adhesion Molecules: Dynamic Molecular and Cellular Mechanisms of Morphogenetic Regulation." Physiological Reviews 91, no. 2 (April 2011): 691–731. http://dx.doi.org/10.1152/physrev.00004.2010.

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This review addresses the cellular and molecular mechanisms of cadherin-based tissue morphogenesis. Tissue physiology is profoundly influenced by the distinctive organizations of cells in organs and tissues. In metazoa, adhesion receptors of the classical cadherin family play important roles in establishing and maintaining such tissue organization. Indeed, it is apparent that cadherins participate in a range of morphogenetic events that range from support of tissue integrity to dynamic cellular rearrangements. A comprehensive understanding of cadherin-based morphogenesis must then define the molecular and cellular mechanisms that support these distinct cadherin biologies. Here we focus on four key mechanistic elements: the molecular basis for adhesion through cadherin ectodomains, the regulation of cadherin expression at the cell surface, cooperation between cadherins and the actin cytoskeleton, and regulation by cell signaling. We discuss current progress and outline issues for further research in these fields.

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Bazzoni, Gianfranco, Maria Grazia Lampugnani, and Elisabetta Dejana. "The Role of Endothelial Cell-to-Cell Junctions in Vascular Morphogenesis." Thrombosis and Haemostasis 82, no. 08 (1999): 755–61. http://dx.doi.org/10.1055/s-0037-1615908.

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IntroductionAdhesion of endothelial cells (ECs) to one another and to the extracellular matrix is mediated by various surface receptors These surface receptors belong to several families of ubiquitously expressed cell adhesion molecules, such as cadherins integrins, immunoglobulins, and proteoglycans. Besides merely providing attachment sites, most adhesive receptors interac with cytoskeletal and cytoplasmic molecules and, thus, contribute to the regulation of cell morphology and signaling.Adhesion requires refined modulation to sustain the process of new vessel formation or angiogenesis. Adjoining cells mus act in concert to finalize migration and proliferation and organize into a three-dimensional network of patent tubes. Some of the molecules involved in these cell-to-extracellular matrix and cell-to-cell interactions have now been characterized. The intracellular signaling pathways activated by these molecules are, on the contrary, still rather obscure. Moreover, the adhesive systems to matrix and neighboring cells can communicate,1-4 adding complexity and coordination to the process.

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Machnicka, Beata, Renata Grochowalska, Dżamila M. Bogusławska, and Aleksander F. Sikorski. "The role of spectrin in cell adhesion and cell–cell contact." Experimental Biology and Medicine 244, no. 15 (June 21, 2019): 1303–12. http://dx.doi.org/10.1177/1535370219859003.

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Spectrins are proteins that are responsible for many aspects of cell function and adaptation to changing environments. Primarily the spectrin-based membrane skeleton maintains cell membrane integrity and its mechanical properties, together with the cytoskeletal network a support cell shape. The occurrence of a variety of spectrin isoforms in diverse cellular environments indicates that it is a multifunctional protein involved in numerous physiological pathways. Participation of spectrin in cell–cell and cell–extracellular matrix adhesion and formation of dynamic plasma membrane protrusions and associated signaling events is a subject of interest for researchers in the fields of cell biology and molecular medicine. In this mini-review, we focus on data concerning the role of spectrins in cell surface activities such as adhesion, cell–cell contact, and invadosome formation. We discuss data on different adhesion proteins that directly or indirectly interact with spectrin repeats. New findings support the involvement of spectrin in cell adhesion and spreading, formation of lamellipodia, and also the participation in morphogenetic processes, such as eye development, oogenesis, and angiogenesis. Here, we review the role of spectrin in cell adhesion and cell–cell contact.Impact statementThis article reviews properties of spectrins as a group of proteins involved in cell surface activities such as, adhesion and cell–cell contact, and their contribution to morphogenesis. We show a new area of research and discuss the involvement of spectrin in regulation of cell–cell contact leading to immunological synapse formation and in shaping synapse architecture during myoblast fusion. Data indicate involvement of spectrins in adhesion and cell–cell or cell–extracellular matrix interactions and therefore in signaling pathways. There is evidence of spectrin’s contribution to the processes of morphogenesis which are connected to its interactions with adhesion molecules, membrane proteins (and perhaps lipids), and actin. Our aim was to highlight the essential role of spectrin in cell–cell contact and cell adhesion.

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Shim, Katherine, Kimberly J. Blake, Joseph Jack, and Mark A. Krasnow. "TheDrosophila ribbongene encodes a nuclear BTB domain protein that promotes epithelial migration and morphogenesis." Development 128, no. 23 (December 1, 2001): 4923–33. http://dx.doi.org/10.1242/dev.128.23.4923.

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During development of the Drosophila tracheal (respiratory) system, the cell bodies and apical and basal surfaces of the tracheal epithelium normally move in concert as new branches bud and grow out to form tubes. We show that mutations in the Drosophila ribbon (rib) gene disrupt this coupling: the basal surface continues to extend towards its normal targets, but movement and morphogenesis of the tracheal cell bodies and apical surface is severely impaired, resulting in long basal membrane protrusions but little net movement or branch formation. rib mutant tracheal cells are still responsive to the Branchless fibroblast growth factor (FGF) that guides branch outgrowth, and they express apical membrane markers normally. This suggests that the defect lies either in transmission of the FGF signal from the basal surface to the rest of the cell or in the apical cell migration and tubulogenesis machinery. rib encodes a nuclear protein with a BTB/POZ domain and Pipsqueak DNA-binding motif. It is expressed in the developing tracheal system and other morphogenetically active epithelia, many of which are also affected in rib mutants. We propose that Rib is a key regulator of epithelial morphogenesis that promotes migration and morphogenesis of the tracheal cell bodies and apical surface and other morphogenetic movements.

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NIKOLAOU, S., and R. B. GASSER. "Extending from PARs in Caenorhabditis elegans to homologues in Haemonchus contortus and other parasitic nematodes." Parasitology 134, no. 4 (November 16, 2006): 461–82. http://dx.doi.org/10.1017/s0031182006001727.

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Signal transduction molecules play key roles in the regulation of developmental processes, such as morphogenesis, organogenesis and cell differentiation in all organisms. They are organized into ‘pathways’ that represent a coordinated network of cell-surface receptors and intracellular molecules, being involved in sensing environmental stimuli and transducing signals to regulate or modulate cellular processes, such as gene expression and cytoskeletal dynamics. A particularly important group of molecules implicated in the regulation of the cytoskeleton for the establishment and maintenance of cell polarity is the PAR proteins (derived from partition defective in asymmetric cell division). The present article reviews salient aspects of PAR proteins involved in the early embryonic development and morphogenesis of the free-living nematode Caenorhabditis elegans and some other organisms, with an emphasis on the molecule PAR-1. Recent advances in the knowledge and understanding of PAR-1 homologues from the economically important parasitic nematode, Haemonchus contortus, of small ruminants is summarized and discussed in the context of exploring avenues for future research in this area for parasitic nematodes.

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Brown, Nicholas H., James W. Bloor, Olga Dunin-Borkowski, and M. Dolores Martín-Bermudo. "lntegrins and morphogenesis." Development 119, Supplement (December 1, 1993): 177–83. http://dx.doi.org/10.1242/dev.119.supplement.177.

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The Drosophila position specific (PS) integrins consist of two cell surface heterodimers, PSl (αPs1βPS) and PS2 (αPs2βPS), which are expressed on complementary sides of attachments between cell layers and are essential for these attachments. Current evidence suggests that the PS integrins bind to components of the extracellular matrix, similar to the majority of vertebrate integrins, but specific Drosophila ligands have not yet been identified. In the embryo PSI is found on the surface of the epidermis and endoderm, while PS2 is restricted to the mesoderm. The integrins are concentrated at the sites where the somatic muscles attach to the epidermis and at the interface between the visceral mesoderm and the endoderm. In myospheroid mutant embryos, which lack the rssubunit, the adhesion between the mesoderm and the other cell layers fails. The PS integrins are also required for the adhesion of the dorsal to the ventral surface of the wing during metamorphosis. PSl is expressed on the basal surface of the dorsal cells and PS2 is expressed on the ventral cells. Loss of PS integrin function in the wing results in balloon shaped wings because of the failure of the two surfaces of the wing blade to adhere to each other. These and other aspects of the phenotypes of mutations in the genes encoding the PS integrins indicate that integrins play an important role in the adhesion of different cell layers to each other and thus an essential role in the morphogenesis of the organism. The use of extracellular matrix receptors in this role may aid in keeping the different cell layers distinct.

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Hirai, Yohei, Derek Radisky, Rosanne Boudreau, Marina Simian, Mary E. Stevens, Yumiko Oka, Kyoko Takebe, Shinichiro Niwa, and Mina J. Bissell. "Epimorphin Mediates Mammary Luminal Morphogenesis through Control of C/EBPβ." Journal of Cell Biology 153, no. 4 (May 14, 2001): 785–94. http://dx.doi.org/10.1083/jcb.153.4.785.

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We have shown previously that epimorphin (EPM), a protein expressed on the surface of myoepithelial and fibroblast cells of the mammary gland, acts as a multifunctional morphogen of mammary epithelial cells. Here, we present the molecular mechanism by which EPM mediates luminal morphogenesis. Treatment of cells with EPM to induce lumen formation greatly increases the overall expression of transcription factor CCAAT/enhancer binding protein (C/EBP)β and alters the relative expression of its two principal isoforms, LIP and LAP. These alterations were shown to be essential for the morphogenetic activities, since constitutive expression of LIP was sufficient to produce lumen formation, whereas constitutive expression of LAP blocked EPM-mediated luminal morphogenesis. Furthermore, in a transgenic mouse model in which EPM expression was expressed in an apolar fashion on the surface of mammary epithelial cells, we found increased expression of C/EBPβ, increased relative expression of LIP to LAP, and enlarged ductal lumina. Together, our studies demonstrate a role for EPM in luminal morphogenesis through control of C/EBPβ expression.

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Clark, Andrew G., Ortrud Wartlick, Guillaume Salbreux, and Ewa K. Paluch. "Stresses at the Cell Surface during Animal Cell Morphogenesis." Current Biology 24, no. 10 (May 2014): R484—R494. http://dx.doi.org/10.1016/j.cub.2014.03.059.

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Yamamoto, A., S. L. Amacher, S. H. Kim, D. Geissert, C. B. Kimmel, and E. M. De Robertis. "Zebrafish paraxial protocadherin is a downstream target of spadetail involved in morphogenesis of gastrula mesoderm." Development 125, no. 17 (September 1, 1998): 3389–97. http://dx.doi.org/10.1242/dev.125.17.3389.

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Zebrafish paraxial protocadherin (papc) encodes a transmembrane cell adhesion molecule (PAPC) expressed in trunk mesoderm undergoing morphogenesis. Microinjection studies with a dominant-negative secreted construct suggest that papc is required for proper dorsal convergence movements during gastrulation. Genetic studies show that papc is a close downstream target of spadetail, gene encoding a transcription factor required for mesodermal morphogenetic movements. Further, we show that the floating head homeobox gene is required in axial mesoderm to repress the expression of both spadetail and papc, promoting notochord and blocking differentiation of paraxial mesoderm. The PAPC structural cell-surface protein may provide a link between regulatory transcription factors and the actual cell biological behaviors that execute morphogenesis during gastrulation.

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Trautman, M. S., J. Kimelman, and M. Bernfield. "Developmental expression of syndecan, an integral membrane proteoglycan, correlates with cell differentiation." Development 111, no. 1 (January 1, 1991): 213–20. http://dx.doi.org/10.1242/dev.111.1.213.

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Syndecan is an integral membrane proteoglycan that behaves as a matrix receptor by binding cells to interstitial matrix and associating intracellularly with the actin cytoskeleton. Using immunohistology, we have now localized this proteoglycan during the morphogenesis of various derivatives of the surface ectoderm in mouse embryos. Syndecan is expressed on ectodermal epithelia, but is selectively lost from the cells that differentiate into the localized placodes that initiate lens, nasal, otic and vibrissal development. The loss is transient on presumptive ear, nasal and vibrissal epithelia; the derivatives of the differentiating ectodermal cells that have lost syndecan subsequently re-express syndecan. In contrast, syndecan is initially absent from the mesenchyme underlying the surface ectoderm, and is transiently expressed when the surface ectoderm loses syndecan. These results demonstrate that expression of syndecan is developmentally regulated in a distinct spatiotemporal pattern. On epithelia, syndecan is lost at a time and, location that correlates with epithelial cell differentiation and, on mesenchyme, syndecan is acquired when the cells aggregate in proximity to the epithelium. This pattern of change with morphogenetic events is unique and not duplicated by other matrix molecules or adhesion receptors.

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Dissertations / Theses on the topic "Cell surface molecules][Morphogenesis"

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Hinton, I. E. "The developmental biology of Drosophila cell surfaces." Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233464.

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Kaplan, Elizabeth Danford. "Cell adhesion molecules in human hair follicle morphogenesis /." Thesis, Connect to this title online; UW restricted, 1996. http://hdl.handle.net/1773/5688.

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Preston, Alexandra McEwan. "Interactions of immunoglobulin superfamily leukocyte cell surface molecules." Thesis, University of Oxford, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.318630.

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Snell, Daniel C. "Cell-surface molecules of developing chicken B cells." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326977.

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Tasker, Lynn. "Cell surface molecules involved in the regulation of B cell activation." Thesis, University of Liverpool, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261832.

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Morris, L. "Expression of surface molecules on mouse foetal macrophages." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235069.

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Tennant, Ian. "Antibody-based strategies for identifying novel apoptotic-cell surface-associated molecules." Thesis, University of Edinburgh, 2005. http://hdl.handle.net/1842/29395.

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Defective clearance of apoptotic cells (ACs) is linked to autoimmune and inflammatory disease states such as systemic lupus erythematosus and cystic fibrosis. Relatively few markers exist for the ‘eat me’ signals displayed on the AC surface despite the great potential for such molecules as diagnostic or therapeutic reagents. In this work various antibody-based strategies were employed in an attempt to identify novel AC-specific epitopes. An initial strategy utilised a phage displayed antibody library containing a repertoire of ~10⁸ antibody fragments encoded by human germline genes as an unbiased source of binding specificity. An alternative approach was based on the knowledge that receptors used by macrophages to recognise ACs also recognise pathogen-associated molecules. By looking for the ability of antibodies raised against pathogens to cross-react with ACs the hypothesis that cells undergoing apoptosis reveal molecular patterns that resemble those on pathogen related structures was tested. Screening of antibodies raised in vivo, that have previously been characterised as having specificity for pathogen-associated molecular patterns (PAMPs) revealed that some cross-react with cells undergoing apoptosis. One of these antibodies was found to bind an epitope found on the ubiquitously expressed ~40KDa precursor to Laminin-Binding-Protein (LBP/p40). These findings suggest that epitopes resembling PAMPs appear on the surface of mammalian cells as a result of apoptosis and that these epitopes can be found on endogenously expressed molecules which are normally excluded from the surface of viable cells. The ability of host receptors to cross-react with host and pathogen-associated epitopes in this way may lead to a greater understanding of the mechanisms of autoimmune reactions and allow design of approaches to stimulate the immune system for the treatment of cancer.

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Bloom, Stuart. "Adhesion molecules in the gastrointestinal tract : a search for cell surface molecules upregulated in inflammatory bowel disease." Thesis, University of Oxford, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239338.

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McConnell, Michael James. "Cell-surface Tumoricidal Molecules and NF-kB in the Tumor-burdened Host." Thesis, Virginia Tech, 2002. http://hdl.handle.net/10919/9609.

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Tumor-distal immune suppression promotes tumor growth by preventing the recruitment of leukocytes to the tumor-proximal microenvironment. Tumor necrosis factor (TNF)-a is both secreted by and expressed on the cell-surface (mTNF-a) of macrophages. When stimulated with LPS, tumor-burdened host (TBH) macrophages secrete more TNF-a than normal host (NH) macrophages. In this study, I showed that mTNF-a is elevated both in freshly isolated and stimulated TBH macrophages. Additionally, I analyzed the expression of Fas and FasL on freshly isolated and LPS-stimulated macrophages and found no differences between TBH and NH macrophages. Fas and Fas ligand (FasL) cell-surface expression was analyzed on NH and TBH T-cells. While no difference was observed in freshly isolated cells, cell-surface expression of both proteins remained higher in TBH T-cells than NH T-cells after mitogenic stimulation. Fas and FasL analysis was also extended to the MethKDE fibrosarcoma and I found that these tumor cells express high levels of FasL. Because past observations show increased TNF-a mRNA expression in TBH macrophages relative to NH macrophages, I hypothesized that NF-kB activation may be increased as well. NF-kB is a transcription factor whose activation is required for TNF-a transcription. I observed increased NF-kB activation in both splenic and peritoneal TBH macrophages. Interestingly, electrophoretic mobility shift analysis (EMSA) suggests that different species of NF-kB were found in each distinct population of macrophages. Together, these data demonstrate that cell-surface tumoricidal molecules and NF-kB are dysregulated in the tumor-burdened host.
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Mitakidis, Nikolaos. "Structural studies of cell surface signalling molecules for neuronal guidance and connectivity." Thesis, University of Oxford, 2013. http://ora.ox.ac.uk/objects/uuid:67a41765-afb6-4cbe-ae60-884773127b6c.

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Signal transduction is critical during the lifetime of a neuron as it navigates to reach its targets, forms functional synaptic connections and adjusts the molecular architecture of these connections in an activity-dependent manner. Understanding the molecular organisation of components required for neuronal signalling will provide novel biological insight and can contribute to the design of therapeutics for neurodevelopmental and neurodegenerative disorders. The focus of the thesis is on determining mechanistic molecular details of a number of distinct cell surface systems implicated in neuronal signalling. Crystallographic studies on the cell surface complex between Eph receptor A4 and ephrinA5 contributed to understanding how the modes of higher order arrangements of receptors involved in guidance affect signal transduction across the membrane. A set of structural and biophysical studies addressed the proteoglycan regulation of RPTPσ-TrkCtrans-synaptic interaction and contributed to deciphering the principles of the switch from axonal growth to synapse establishment and formation. A crystallographic and biochemical analysis of the neuronal C1q-like family, enabled mapping their interactions with potential synaptic partners, and guided functional studies aimed at elucidating their roles in the maintenance of synaptic integrity. Preliminary work on the neuronal Sigma-1 receptor chaperone laid the foundations for the structural determination of this receptor.

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Books on the topic "Cell surface molecules][Morphogenesis"

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Chattopadhyay, Kausik, and Subhash C. Basu, eds. Biochemical and Biophysical Roles of Cell Surface Molecules. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-3065-0.

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Surface and interfacial aspects of cell adhesion. Leiden: Boston, 2010.

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The cell surface in embryogenesis and carcinogenesis. Caldwell, N.J: Telford Press, 1989.

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Cole, Louise. Immunocytochemical studies of fungal cell surface molecules and the vicia faba-Botrytis interaction. Oxford: Oxford Brookes University, 1996.

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Michaela, Kendall, Rehfeldt Florian, and SpringerLink (Online service), eds. Adhesion of Cells, Viruses and Nanoparticles. Dordrecht: Springer Science+Business Media B.V., 2011.

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Malcolm, Steinberg, ed. The Cell surface in development and cancer. New York: Plenum Press, 1986.

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Biochemical and Biophysical Roles of Cell Surface Molecules. Springer, 2019.

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Developmental Biology:A Comprehensive Synthesis: Volume 3: The Cell Surface in Development and Cancer (Developmental Biology). Springer, 1986.

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Yamagata, Masahito, and Hiroko Bannai, eds. Neuroscience and Neurotechnology of Neuronal Cell Surface Molecules in Neural Circuits. Frontiers Media SA, 2021. http://dx.doi.org/10.3389/978-2-88971-149-9.

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Lieping, Chen, ed. The B7-CD28 family molecules. Georgetown, Tex: Landes Bioscience/Eurekah.com, 2003.

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Book chapters on the topic "Cell surface molecules][Morphogenesis"

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Hart, D. N. J., G. J. Clark, J. W. Dekker, D. B. Fearnley, M. Kato, B. D. Hock, A. D. McLellan, et al. "Dendritic Cell Surface Molecules." In Advances in Experimental Medicine and Biology, 439–42. Boston, MA: Springer US, 1997. http://dx.doi.org/10.1007/978-1-4757-9966-8_72.

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van Roy, Frans, Volker Nimmrich, Anton Bespalov, Achim Möller, Hiromitsu Hara, Jacob P. Turowec, Nicole A. St. Denis, et al. "Cell Surface Glycoprotein CD53." In Encyclopedia of Signaling Molecules, 386. New York, NY: Springer New York, 2012. http://dx.doi.org/10.1007/978-1-4419-0461-4_100245.

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Pickett-Heaps, J. D., Jocelyn Carpente, and A. Koutoulis. "Valve and seta (spine) morphogenesis in the centric diatom Chaetoceros peruvianus Brightwell." In The Protistan Cell Surface, 269–82. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9378-5_16.

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Turner, David C. "Cell—Cell and Cell—Matrix Interactions in the Morphogenesis of Skeletal Muscle." In The Cell Surface in Development and Cancer, 205–24. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5050-7_11.

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Schmid, Anna-Maria M. "Aspects of morphogenesis and function of diatom cell walls with implications for taxonomy." In The Protistan Cell Surface, 43–60. Vienna: Springer Vienna, 1994. http://dx.doi.org/10.1007/978-3-7091-9378-5_3.

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Spooner, Brian S., Holly A. Thompson-Pletscher, Brad Stokes, and Kenneth E. Bassett. "Extracellular Matrix Involvement in Epithelial Branching Morphogenesis." In The Cell Surface in Development and Cancer, 225–60. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5050-7_12.

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Harris, Albert K. "Cell Traction in Relationship to Morphogenesis and Malignancy." In The Cell Surface in Development and Cancer, 339–57. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5050-7_16.

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Steinberg, Malcolm S. "Cell Surfaces in the Control of Growth and Morphogenesis." In The Cell Surface in Development and Cancer, 1–13. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-5050-7_1.

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Albersheim, Peter, Alan G. Darvill, Keith R. Davis, Steven H. Doares, David J. Gollin, Roger O’Neill, Patrick R. Toubart, and William S. York. "Oligosaccharins - Complex Carbohydrate Regulatory Molecules." In The Cell Surface in Signal Transduction, 147–49. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72910-2_11.

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Sára, M., and U. B. Sleytr. "Charge Distribution of S-Layers and Importance of Charged Groups for Morphogenesis and Function." In Crystalline Bacterial Cell Surface Layers, 105–8. Berlin, Heidelberg: Springer Berlin Heidelberg, 1988. http://dx.doi.org/10.1007/978-3-642-73537-0_23.

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Conference papers on the topic "Cell surface molecules][Morphogenesis"

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Meng, Boyu, Rendall R. Strawbridge, Kenneth Tichauer, Kimberley S. Samkoe, and Scott C. Davis. "Monitoring cancer cell surface receptor expression during anti-angiogenesis therapy in vivo." In Molecular-Guided Surgery: Molecules, Devices, and Applications VII, edited by Summer L. Gibbs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2021. http://dx.doi.org/10.1117/12.2583237.

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Nerurkar, Nandan L., and Clifford J. Tabin. "Cell Velocity Gradients Underlie Early Morphogenesis of the Avian Gut Tube." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80898.

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At the end of gastrulation, the endoderm forms the ventral surface of the developing embryo. Subsequently, through a series of poorly understood morphogenetic events, the initially flat endoderm is transformed into the gut tube, a cylindrical structure that gives rise to the epithelial lining of the entire respiratory and gastrointestinal tracts. At present there is no mechanistic understanding of how the endoderm is transformed from a planar sheet to a simple tube. In avian and mammalian species, formation of the gut tube begins with two invaginations at the anterior and posterior poles of the embryo, termed the anterior (AIP) and caudal intestinal portals (CIP). The AIP, which forms the foregut, and CIP which forms the hindgut, begin moving toward one another, “zipping” the gut tube closed along the embryonic midline (Fig. 1A). The AIP and CIP meet at the umbilicus (mammals) or yolk stalk (avian), where the midgut is formed.

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Nerurkar, Nandan L., and Cliff J. Tabin. "Collective Cell Movements Drive Morphogenesis and Elongation of the Avian Hindgut." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14438.

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At the end of gastrulation, the endoderm forms a single-cell thick epithelium lining the ventral surface of the developing embryo. Subsequently, through a series of poorly understood events, the initially flat endoderm is transformed into the gut tube, a cylindrical structure that gives rise to the epithelial lining of the entire respiratory and gastrointestinal tracts. In birds and mammals, formation of the gut tube begins with two invaginations at the anterior (head) and posterior (tail) poles of the embryo, termed the anterior (AIP) and caudal intestinal portals (CIP). It is thought that the AIP and CIP begin moving toward one another as two progressing waves of lateral-to medial folding (from left and right toward center), “zipping” the gut tube closed along the embryonic midline (Fig. 1A). This view of lateral-to-medial folding is, however, inconsistent with several observations. For example, fate mapping studies in chick and mouse that suggest that cells originating in the posterior end (toward the tail) of the flat endoderm do not form the hindgut, but instead contribute to the more anterior midgut [1, 2]. This would not be possible in a simple lateral-to-medial folding process. Therefore, it is largely unknown how this fundamental structure of the vertebrate body plan is established. The objective of the present work is to apply multi-photon live imaging of the chick embryo to determine how the hindgut is formed. Our findings suggest the hindgut arises from directed, collective cell movements that drive antero-posterior folding of the initially flat endoderm.

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Hoballah, Jawad, German Gonzalez, Sinyoung Jeong, Hongzhou Ma, Jeffrey S. Brooker, Daniel W. Cramer, Petra B. Krauledat, Conor L. Evans, and W. Peter Hansen. "Quantification of Low Abundance White Cell Surface Molecules in Ovarian Cancer by Dark Field and Fluorescence Microscopy." In Bio-Optics: Design and Application. Washington, D.C.: OSA, 2019. http://dx.doi.org/10.1364/boda.2019.jw4c.1.

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5

Evans, Conor L. "Highly Sensitive and Reliable Plasmonic Nanoparticle-based Microscopy Method for Quantification of Low Abundance Cell Surface Molecules." In Novel Techniques in Microscopy. Washington, D.C.: OSA, 2017. http://dx.doi.org/10.1364/ntm.2017.jtu1c.3.

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6

Yamane, Hiromichi, Hideko Isozaki, Nobuaki Ochi, Kenichiro Kudo, Yoshihiro Honda, Tomoko Yamagishi, Toshio Kubo, Katsuyuki Kiura, and Nagio Takigawa. "Abstract 1323: Both programmed cell death protein 1 and programmed death-ligand 1 molecules can be expressed on the cell surface of small-cell lung cancer." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1323.

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7

Hsieh, Chien-Te, Kuen-Song Lin, Shih Hung Chan, and Ay Su. "Fabrication of Composite Carbon Nanotubes With Different Oxidation Levels by a Self-Assembly Surface Modification." In ASME 2006 4th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2006. http://dx.doi.org/10.1115/fuelcell2006-97174.

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Abstract:

An efficient technique to fabricate metal-oxide/carbon composite nanotubes has been developed through a self-assembly processing that includes implantation of acidic groups and interaction between surface oxides and metal ions or hydration molecules. To functionalize carbon nanotubes, gaseous oxidation at 300 °C was firstly employed to build functional oxygen groups including carboxyl, carbonyl and hydroxyl group, on the ends or sidewalls of the nanotubes. It revealed that the oxidized nanotubes express a slight improvement of surface hydrophilicity, which was demonstrated by contact angle measurement. X-ray photoelectron spectroscope investigation indicated that the ratio of attached metal-oxide onto the oxidized nanotubes gradually increases with oxidation level, i.e., surface O/C atomic ratio. This evidence reflected that the surface oxides act as an adsorption center that strongly interacts with metal ions or hydration molecules in aqueous phase. Applying this method, SnO2, RuO2, NiO and PtRu nanoparticles having an average size of 5 nm were assembled on the oxidized carbon nanotubes.

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8

Haertel, B., U. Lindequist, M. Haehnel, K. Wende, K. Oehmigen, and T. von Woedtke. "Plasma-cell-interaction: Expression of surface molecules on HaCaT keratinocytes after treatment with dielectric barrier discharge (DBD) plasma." In 2011 IEEE 38th International Conference on Plasma Sciences (ICOPS). IEEE, 2011. http://dx.doi.org/10.1109/plasma.2011.5993207.

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9

Kim, Hyonchol, Koudai Oikawa, and Kenji Yasuda. "Quantitative observation of membrane-attached bio-molecules on a cell surface using gold nano-particle and atomic force microscopy." In 2007 Digest of papers Microprocesses and Nanotechnology. IEEE, 2007. http://dx.doi.org/10.1109/imnc.2007.4456210.

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Tarhoni, Imad, Mary Jo Fidler, Ibtihaj Fughhi, Connor Wakefield, Revathi Kollipara, Maneet Multani, Marta Batus, et al. "Abstract 404: Prognostic value of soluble and cell surface immune-checkpoint molecules in advanced non-small cell lung cancer (NSCLC) patients receiving anti-PD-1/-L1 immunotherapy." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-404.

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Reports on the topic "Cell surface molecules][Morphogenesis"

1

Al-Attar, Ali. Cell Surface Molecules Driving Breast Cancer/Endothelial Interactions. Fort Belvoir, VA: Defense Technical Information Center, July 2001. http://dx.doi.org/10.21236/ada396252.

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2

Al-Attar, Ali. Cell Surface Molecules Driving Breast Cancer/Endothelial Interactions. Fort Belvoir, VA: Defense Technical Information Center, July 2002. http://dx.doi.org/10.21236/ada409628.

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