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Journal articles on the topic '110902 Cellular Nervous System'

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Author: Grafiati

Published: 10 December 2022

Last updated: 28 January 2023

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1

Díaz-Balzac, Carlos A., Lionel D. Vázquez-Figueroa, and José E. García-Arrarás. "Novel markers identify nervous system components of the holothurian nervous system." Invertebrate Neuroscience 14, no. 2 (April 17, 2014): 113–25. http://dx.doi.org/10.1007/s10158-014-0169-1.

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2

Dockray, Graham. "The enteric nervous system." Neurochemistry International 12, no. 1 (January 1988): 103. http://dx.doi.org/10.1016/0197-0186(88)90156-8.

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3

Leonard, B. E. "The Cellular Structure of the Mammalian Nervous System." Neurochemistry International 11, no. 2 (January 1987): 249–50. http://dx.doi.org/10.1016/0197-0186(87)90020-9.

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4

Philbert, M. A., D. K. Waters, and H. E. Lowndes. "Cellular distribution of glutathione in the nervous system." Free Radical Biology and Medicine 9 (January 1990): 20. http://dx.doi.org/10.1016/0891-5849(90)90239-f.

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5

Brown, MarvinR, Jean Rivier, and Laurel Fisher. "Bombesin: Central nervous system actions to affect the autonomic nervous system." Regulatory Peptides 19, no. 1-2 (October 1987): 102. http://dx.doi.org/10.1016/0167-0115(87)90082-6.

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6

Flachenecker, Peter, and Karlheinz Reiners. "Autonomic nervous system testing." Muscle & Nerve 21, no. 5 (May 1998): 680. http://dx.doi.org/10.1002/(sici)1097-4598(199805)21:5<680::aid-mus25>3.0.co;2-y.

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7

Chen, H. S. "Immune Response in the Nervous System." Journal of Chemical Neuroanatomy 25, no. 4 (July 2003): 311. http://dx.doi.org/10.1016/s0891-0618(03)00020-6.

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8

Barnard, Eric A., Joseph Simon, and Tania E. Webb. "Nucleotide receptors in the nervous system." Molecular Neurobiology 15, no. 2 (October 1997): 103–29. http://dx.doi.org/10.1007/bf02740631.

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9

Yepes, Manuel. "TWEAK and the Central Nervous System." Molecular Neurobiology 35, no. 3 (August 1, 2007): 255–65. http://dx.doi.org/10.1007/s12035-007-0024-z.

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10

Breakefield, Xandra O., and Alfred I. Geller. "Gene transfer into the nervous system." Molecular Neurobiology 1, no. 4 (December 1987): 339–71. http://dx.doi.org/10.1007/bf02935741.

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11

Mayer, RJ. "Ubiquitin and the nervous system." Neurochemistry International 21 (January 1992): S3. http://dx.doi.org/10.1016/0197-0186(92)90011-f.

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12

Iqbal, Sameera, Mina Ghanimi Fard, Arun Everest-Dass, Nicolle H. Packer, and Lindsay M. Parker. "Understanding cellular glycan surfaces in the central nervous system." Biochemical Society Transactions 47, no. 1 (December 17, 2018): 89–100. http://dx.doi.org/10.1042/bst20180330.

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Abstract Glycosylation, the enzymatic process by which glycans are attached to proteins and lipids, is the most abundant and functionally important type of post-translational modification associated with brain development, neurodegenerative disorders, psychopathologies and brain cancers. Glycan structures are diverse and complex; however, they have been detected and targeted in the central nervous system (CNS) by various immunohistochemical detection methods using glycan-binding proteins such as anti-glycan antibodies or lectins and/or characterized with analytical techniques such as chromatography and mass spectrometry. The glycan structures on glycoproteins and glycolipids expressed in neural stem cells play key roles in neural development, biological processes and CNS maintenance, such as cell adhesion, signal transduction, molecular trafficking and differentiation. This brief review will highlight some of the important findings on differential glycan expression across stages of CNS cell differentiation and in pathological disorders and diseases such as Alzheimer's disease, Parkinson's disease, Huntington's disease, multiple sclerosis, amyotrophic lateral sclerosis, schizophrenia and brain cancer.

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13

Saffrey, M. Jill. "Cellular changes in the enteric nervous system during ageing." Developmental Biology 382, no. 1 (October 2013): 344–55. http://dx.doi.org/10.1016/j.ydbio.2013.03.015.

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14

Campos-Ortega, J. "Cellular interactions in the developing nervous system of Drosophila." Cell 77, no. 7 (July 1, 1994): 969–75. http://dx.doi.org/10.1016/0092-8674(94)90437-5.

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15

Hardy, Paul A. "Genetic Aspects of Nervous System Development." Journal of Neurogenetics 6, no. 3 (January 1990): 115–31. http://dx.doi.org/10.3109/01677069009107105.

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16

Forbes, Lindsey H., and Veronique E. Miron. "Monocytes in central nervous system remyelination." Glia 70, no. 5 (October 28, 2021): 797–807. http://dx.doi.org/10.1002/glia.24111.

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17

González-Jamett, Arlek M., Valentina Haro-Acuña, Fanny Momboisse, Pablo Caviedes, Jorge A. Bevilacqua, and Ana M. Cárdenas. "Dynamin-2 in nervous system disorders." Journal of Neurochemistry 128, no. 2 (October 23, 2013): 210–23. http://dx.doi.org/10.1111/jnc.12455.

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18

Chen, Pan, Sudipta Chakraborty, Somshuvra Mukhopadhyay, Eunsook Lee, Monica M. B. Paoliello, Aaron B. Bowman, and Michael Aschner. "Manganese homeostasis in the nervous system." Journal of Neurochemistry 134, no. 4 (June 16, 2015): 601–10. http://dx.doi.org/10.1111/jnc.13170.

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19

Fox, M. "Symposium S03: Wiring the nervous system." Journal of Neurochemistry 94 (June 2005): 53. http://dx.doi.org/10.1111/j.1474-1644.2005.03229_2.x.

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20

Zhou, Qiang, and Morgan Sheng. "NMDA receptors in nervous system diseases." Neuropharmacology 74 (November 2013): 69–75. http://dx.doi.org/10.1016/j.neuropharm.2013.03.030.

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21

Lee, J. C., M. Mayer-Proschel, and M. S. Rao. "Gliogenesis in the central nervous system." Glia 30, no. 2 (April 2000): 105–21. http://dx.doi.org/10.1002/(sici)1098-1136(200004)30:2<105::aid-glia1>3.0.co;2-h.

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22

Leslie, John B., and W. David Watkins. "Eicosanoids in the central nervous system." Journal of Neurosurgery 63, no. 5 (November 1985): 659–68. http://dx.doi.org/10.3171/jns.1985.63.5.0659.

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✓ All mammalian tissue investigated to date is capable of eicosanoid biosynthesis in response to various activating stimuli. While the importance of these metabolites as major mediators of many normal physiological processes and some pathophysiological conditions has not been proven, it is evident that these compounds are at least important modulators of many cellular and organ system functions. This review is intended to provide the reader with a brief overview of eicosanoid biology, with specific reference to the neurosciences. The increasing knowledge about the role of the eicosanoids in neurobiology may contribute to the understanding and treatment of many neurological diseases. The eicosanoids comprise several groups of biologically active unsaturated fatty acids: the “primary” prostaglandins, the cyclic endoperoxides, the prostanoids, the leukotrienes, and other acid lipids. This article includes a review of the enzymatic pathways of biosynthesis and metabolism of eicosanoids in man, and the pertinent structural nomenclature. The general basic and clinical pharmacological effects of the more important compounds on vascular perfusion, platelet function, intracellular enzyme activity, and interactions with other mediators of cellular activity are reviewed. A more detailed review of the actions of eicosanoids as mediators or modifiers of central nervous system physiology and pathophysiology is presented. Recent animal and human studies on the use and alterations of the eicosanoid metabolites is summarized, specifically where they relate to several clinical problem areas of interest to the neurosurgeon and neurobiologist. These areas include cerebrovascular circulation physiology, cerebral ischemia, cerebral vasospasm following subarachnoid hemor-rhage, migraine headaches, hypothalamic function, neurotransmission, and nociception. A bibliography of 92 articles for further review is also included.

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23

Abdel Hafez, Sara Mohamed Naguib. "Can Covid-19 attack our nervous system?" Journal of Chemical Neuroanatomy 117 (November 2021): 102006. http://dx.doi.org/10.1016/j.jchemneu.2021.102006.

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24

Mena, H., J. L. Ribas, G. Pezeshkpour, J. E. Parisi, and D. Cowan. "CENTRAL NERVOUS SYSTEM HEMANGIOPERICYTOMA." Journal of Neuropathology and Experimental Neurology 48, no. 3 (May 1989): 358. http://dx.doi.org/10.1097/00005072-198905000-00177.

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25

Gilden, Donald H., Ravi Mahalingam, Randall J. Cohrs, and Kenneth L. Tyler. "Herpesvirus infections of the nervous system." Nature Clinical Practice Neurology 3, no. 2 (February 2007): 82–94. http://dx.doi.org/10.1038/ncpneuro0401.

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26

Billingsley, Melvin L., and Walter Lovenberg. "Protein carboxylmethylation and nervous system function." Neurochemistry International 7, no. 4 (January 1985): 575–87. http://dx.doi.org/10.1016/0197-0186(85)90054-3.

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27

Turner, A. J. "Membrane peptidases of the nervous system." Neurochemistry International 7, no. 2 (January 1985): 385–87. http://dx.doi.org/10.1016/0197-0186(85)90130-5.

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28

Davies, W. E. "Trauma of the Central Nervous System." Neurochemistry International 9, no. 2 (January 1986): 350. http://dx.doi.org/10.1016/0197-0186(86)90073-2.

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29

Glover, Joel C. "Introduction: Retinoids and the nervous system." Journal of Neurobiology 66, no. 7 (2006): 603–5. http://dx.doi.org/10.1002/neu.20263.

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30

Marois, Rene, and Thomas J. Carew. "The gastropod nervous system in metamorphosis." Journal of Neurobiology 21, no. 7 (October 1990): 1053–71. http://dx.doi.org/10.1002/neu.480210710.

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31

Mikol, Daniel D., and Eva L. Feldman. "Neurophilins and the nervous system." Muscle & Nerve 22, no. 10 (October 1999): 1337–40. http://dx.doi.org/10.1002/(sici)1097-4598(199910)22:10<1337::aid-mus1>3.0.co;2-w.

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32

Jarrin, Sarah, Sílvia Cabré, and Eilís Dowd. "The potential of biomaterials for central nervous system cellular repair." Neurochemistry International 144 (March 2021): 104971. http://dx.doi.org/10.1016/j.neuint.2021.104971.

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33

Wyss, Livia S., Samuel R. Bray, and Bo Wang. "Cellular diversity and developmental hierarchy in the planarian nervous system." Current Opinion in Genetics & Development 76 (October 2022): 101960. http://dx.doi.org/10.1016/j.gde.2022.101960.

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34

Ali-Osman, Francis, and Deborah Schofield. "Cellular and molecular studies in brain and nervous system oncology." Current Opinion in Oncology 2, no. 4 (August 1990): 655–65. http://dx.doi.org/10.1097/00001622-199002040-00002.

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35

Ali-Osman, Francis, and Deborah Schofield. "Cellular and molecular studies in brain and nervous system oncology." Current Opinion in Oncology 2, no. 4 (August 1990): 655–65. http://dx.doi.org/10.1097/00001622-199008000-00002.

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36

Grafe, P., and K. Ballanyi. "Cellular mechanisms of potassium homeostasis in the mammalian nervous system." Canadian Journal of Physiology and Pharmacology 65, no. 5 (May 1, 1987): 1038–42. http://dx.doi.org/10.1139/y87-164.

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Double-barrelled ion-sensitive microelectrodes were used to measure changes in the intracellular activities of K+, Na+, and Cl− (aKi, aNai, aCli) in neurones of rat sympathetic ganglia and in glial cells of slices from guinea-pig olfactory cortex. In sympathetic neurones, carbachol and γ-aminobutyric acid (GABA) produced a reversible decrease of aKi. The decrease of aKi during carbachol was accompanied by a rise of aNai, whereas in the presence of GABA decreases of aKi and aCli were seen. The reuptake of K+ released during the action of carbachol was completely blocked by ouabain, whereas furosemide inhibited the aKi recovery after the action of GABA. In glial cells, in contrast to the observations in the sympathetic neurones, aKi and aCli increased, whereas aNai decreased when neuronal activity was enhanced by repetitive stimulation of the lateral olfactory tract. It was found that barium ions and ouabain strongly reduced the activity-related rise of intraglial aKi in slices of guinea-pig olfactory cortex. These data show that mammalian neurones as well as glial cells possess several K+ uptake mechanisms that contribute to potassium homeostasis. Ouabain, furosemide, and Ba2+ are useful pharmacological tools to separate these mechanisms.

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37

DURACK, DAVID T. "Cortisone, cyclosporine and cellular immunity in the central nervous system." Pediatric Infectious Disease Journal 6, no. 12 (December 1987): 1155–57. http://dx.doi.org/10.1097/00006454-198706120-00032.

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38

DURACK, DAVID T. "Cortisone, cyclosporine and cellular immunity in the central nervous system." Pediatric Infectious Disease Journal 6, no. 12 (December 1987): 1155–57. http://dx.doi.org/10.1097/00006454-198712000-00032.

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39

Purohit, Abhilasha, Anguraj Sadanandam, Pavan Myneni, and Rakesh K. Singh. "Semaphorin 5A mediated cellular navigation: Connecting nervous system and cancer." Biochimica et Biophysica Acta (BBA) - Reviews on Cancer 1846, no. 2 (December 2014): 485–93. http://dx.doi.org/10.1016/j.bbcan.2014.09.006.

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40

Dubois-Dalcq, Monique, and Regina Armstrong. "The cellular and molecular events of central nervous system remyelination." BioEssays 12, no. 12 (December 1990): 569–76. http://dx.doi.org/10.1002/bies.950121203.

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41

Smith, Dean O. "Cellular and molecular correlates of aging in the nervous system." Experimental Gerontology 23, no. 4-5 (January 1988): 399–412. http://dx.doi.org/10.1016/0531-5565(88)90045-9.

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42

Jänig, Wilfrid. "Autonomic nervous system and inflammation." Autonomic Neuroscience 182 (May 2014): 1–3. http://dx.doi.org/10.1016/j.autneu.2014.02.002.

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43

Clark, Isaac H., Alex Roman, Emily Fellows, Swathi Radha, Susanna R. Var, Zachary Roushdy, Samuel M. Borer, et al. "Cell Reprogramming for Regeneration and Repair of the Nervous System." Biomedicines 10, no. 10 (October 17, 2022): 2598. http://dx.doi.org/10.3390/biomedicines10102598.

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A persistent barrier to the cure and treatment of neurological diseases is the limited ability of the central and peripheral nervous systems to undergo neuroregeneration and repair. Recent efforts have turned to regeneration of various cell types through cellular reprogramming of native cells as a promising therapy to replenish lost or diminished cell populations in various neurological diseases. This review provides an in-depth analysis of the current viral vectors, genes of interest, and target cellular populations that have been studied, as well as the challenges and future directions of these novel therapies. Furthermore, the mechanisms by which cellular reprogramming could be optimized as treatment in neurological diseases and a review of the most recent cellular reprogramming in vitro and in vivo studies will also be discussed.

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44

David, S., P. E. Braun, D. L. Jackson, V. Kottis, and L. McKerracher. "Laminin overrides the inhibitory effects of peripheral nervous system and central nervous system myelin-derived inhibitors of neurite growth." Journal of Neuroscience Research 42, no. 4 (November 1, 1995): 594–602. http://dx.doi.org/10.1002/jnr.490420417.

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45

Siwicki, K. K., B. S. Beltz, T. L. Schwarz, and E. A. Kravitz. "Proctolin in the lobster nervous system." Peptides 6 (January 1985): 393–402. http://dx.doi.org/10.1016/0196-9781(85)90404-8.

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46

Tarasiuk, Olga, and Arianna Scuteri. "Role of Tunneling Nanotubes in the Nervous System." International Journal of Molecular Sciences 23, no. 20 (October 19, 2022): 12545. http://dx.doi.org/10.3390/ijms232012545.

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Cellular communication and the transfer of information from one cell to another is crucial for cell viability and homeostasis. During the last decade, tunneling nanotubes (TNTs) have attracted scientific attention, not only as a means of direct intercellular communication, but also as a possible system to transport biological cargo between distant cells. Peculiar TNT characteristics make them both able to increase cellular survival capacities, as well as a potential target of neurodegenerative disease progression. Despite TNT formation having been documented in a number of cell types, the exact mechanisms triggering their formation are still not completely known. In this review, we will summarize and highlight those studies focusing on TNT formation in the nervous system, as well as their role in neurodegenerative diseases. Moreover, we aim to stress some possible mechanisms and important proteins probably involved in TNT formation in the nervous system.

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47

Harris, William A. "Genetics and Development of the Nervous System." Journal of Neurogenetics 2, no. 3 (January 1985): 179–96. http://dx.doi.org/10.3109/01677068509100149.

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48

Ghandour, M. Said, Anna-Kaisa Parkkila, Seppo Parkkila, Abdul Waheed, and William S. Sly. "Mitochondrial Carbonic Anhydrase in the Nervous System." Journal of Neurochemistry 75, no. 5 (January 4, 2002): 2212–20. http://dx.doi.org/10.1046/j.1471-4159.2000.0752212.x.

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49

Hucho, Ferdinand, and Victor Tsetlin. "Structural Biology of Key Nervous System Proteins." Journal of Neurochemistry 66, no. 5 (November 23, 2002): 1781–92. http://dx.doi.org/10.1046/j.1471-4159.1996.66051781.x.

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50

HARVEY, J. "Behavioral pharmacology of central nervous system stimulants." Neuropharmacology 26, no. 7 (July 1987): 887–92. http://dx.doi.org/10.1016/0028-3908(87)90066-9.

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