Littérature scientifique sur le sujet « Tubular Progenitor »
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Articles de revues sur le sujet "Tubular Progenitor"
Peired, Anna Julie, Maria Elena Melica, Alice Molli, Cosimo Nardi, Paola Romagnani et Laura Lasagni. « Molecular Mechanisms of Renal Progenitor Regulation : How Many Pieces in the Puzzle ? » Cells 10, no 1 (2 janvier 2021) : 59. http://dx.doi.org/10.3390/cells10010059.
Texte intégralChen, Dong, Zhiyong Chen, Yuning Zhang, Chanyoung Park, Ahmed Al-Omari et Gilbert W. Moeckel. « Role of medullary progenitor cells in epithelial cell migration and proliferation ». American Journal of Physiology-Renal Physiology 307, no 1 (1 juillet 2014) : F64—F74. http://dx.doi.org/10.1152/ajprenal.00547.2013.
Texte intégralGupta, Ashwani Kumar, David Z. Ivancic, Bilal A. Naved, Jason A. Wertheim et Leif Oxburgh. « An efficient method to generate kidney organoids at the air-liquid interface ». Journal of Biological Methods 8, no 2 (29 juin 2021) : e150. http://dx.doi.org/10.14440/jbm.2021.357.
Texte intégralGerges, Daniela, Zsofia Hevesi, Sophie H. Schmidt, Sebastian Kapps, Sahra Pajenda, Barbara Geist, Alice Schmidt, Ludwig Wagner et Wolfgang Winnicki. « Tubular epithelial progenitors are excreted in urine during recovery from severe acute kidney injury and are able to expand and differentiate in vitro ». PeerJ 10 (20 octobre 2022) : e14110. http://dx.doi.org/10.7717/peerj.14110.
Texte intégralMaeshima, Akito, Shunsuke Takahashi, Masao Nakasatomi et Yoshihisa Nojima. « Diverse Cell Populations Involved in Regeneration of Renal Tubular Epithelium following Acute Kidney Injury ». Stem Cells International 2015 (2015) : 1–8. http://dx.doi.org/10.1155/2015/964849.
Texte intégralLi, Ling, Rachel Black, Zhendong Ma, Qiwen Yang, Andrew Wang et Fangming Lin. « Use of mouse hematopoietic stem and progenitor cells to treat acute kidney injury ». American Journal of Physiology-Renal Physiology 302, no 1 (1 janvier 2012) : F9—F19. http://dx.doi.org/10.1152/ajprenal.00377.2011.
Texte intégralWen, Donghai, Li Ni, Li You, Liying Zhang, Yong Gu, Chuan-Ming Hao et Jing Chen. « Upregulation of nestin in proximal tubules may participate in cell migration during renal repair ». American Journal of Physiology-Renal Physiology 303, no 11 (1 décembre 2012) : F1534—F1544. http://dx.doi.org/10.1152/ajprenal.00083.2012.
Texte intégralZhang, Zhao, Diana M. Iglesias, Rachel Corsini, LeeLee Chu et Paul Goodyer. « WNT/β-Catenin Signaling Is Required for Integration of CD24+Renal Progenitor Cells into Glycerol-Damaged Adult Renal Tubules ». Stem Cells International 2015 (2015) : 1–11. http://dx.doi.org/10.1155/2015/391043.
Texte intégralSalikhova, D. I., L. R. Khaerdinova, O. V. Makhnach et D. V. Goldshtein. « Angiogenic properties of glial progenitor cells derived from human induced pluripotent stem cells ». Genes & ; Cells 17, no 2 (25 septembre 2022) : 32–39. http://dx.doi.org/10.23868/202209005.
Texte intégralVolovelsky, Oded, Thi Nguyen, Alison E. Jarmas, Alexander N. Combes, Sean B. Wilson, Melissa H. Little, David P. Witte, Eric W. Brunskill et Raphael Kopan. « Hamartin regulates cessation of mouse nephrogenesis independently of Mtor ». Proceedings of the National Academy of Sciences 115, no 23 (21 mai 2018) : 5998–6003. http://dx.doi.org/10.1073/pnas.1712955115.
Texte intégralThèses sur le sujet "Tubular Progenitor"
LOMBARDI, DUCCIO. « Ruolo della popolazione di progenitori tubulari Pax2+ nella rigenerazione del tubulo renale dopo insufficienza renale acuta ». Doctoral thesis, 2016. http://hdl.handle.net/2158/1020975.
Texte intégralChen, Ting Fang, et 陳庭芳. « Effect of Hepatocellular Carcinoma Cell on Differentiation, Migration, Invasion, and Tubular Structure Formation of Endothelial Progenitor Cell and Outgrowth Endothelial Cell ». Thesis, 2009. http://ndltd.ncl.edu.tw/handle/22565559581923767581.
Texte intégral國立清華大學
分子醫學研究所
97
Angiogenesis not only play a critical role in embryonic development and tissue repair, but also is an important process for tumor growth and metastasis. Recent studies have shown that tumor cells could induce the mobilization of endothelial progenitor cell (EPC) and outgrowth endothelial cell (OEC) from bone marrow via many cytokines, such as GM-CSF、SDF-1 and VEGF. Furthermore, those EPC could migrate and invade to tumor micro-metastatic niche, and gradually differentiate into endothelial like-cell incorporate the growing vasculature. Using ex vitro culture-expanded EPC or OEC transplanted in to the tumor bearing mice, many researches suggest that EPC control the angiogenic switch and OEC facilitate the neoangiogenesis in the tumor progression. However, the underlying interaction mechanism of EPC/OEC and carcinoma cells in the progression of tumor cell remains unclear. Thus, the aim of the present study to elucidate the effect of tumor cell on differentiation, migration, invasion, and tubular structure formation of EPC and OEC, using in vitro co-cultured system. Firstly, we need to identified EPC and OEC derived from peripheral blood mononuclear cells. We found both of EPC and OEC displayed several commonly accepted EPC phenotypes, including spindle/cobblestone morphology, ac-LDL incorporation, UEA-1 binding, and CD31/KDR/Flt-1 reactivity. The previous clinical reports have indicated that hepatocellular carcinoma (HCC) is one of malignant tumor with rich neovascularization, which can be clearly observed in hepatic angiography. On the basis of co-culture transwell model and time-lapse video microscopy system, we show that migration and invasion capability of EPC was augmented by HCC, and also can induce EPC express higher intensity of endothelial markers to promote the differentiation of EPC. On the other hand, the migration, invasion and tubular structure formation of OEC was inhibited by HCC. In addition, HCC did not alter cell cycle of EPC, whereas they prevented OEC from entering S and G2/M phases and induce OEC cell cycle G0/G1 arrest. The present study suggests that the different effect of HCC on EPC and OEC may mediate their different contribution to tumor angiogenesis. Our findings may provide new insights into the interaction mechanism of EPC/OEC and HCC involve in the progression of angiogenesis.
Actes de conférences sur le sujet "Tubular Progenitor"
Feijão, Maria Clara Tomaz, Fernanda Pimentel Arraes Maia, Mateus Coelho Gondim de Oliveira Lima, Vitória Moreira Soares et Luiz Gonzaga Porto Pinheiro. « CONCERNING A FAMILY WITH BRCA2 MUTATION ». Dans XXIV Congresso Brasileiro de Mastologia. Mastology, 2022. http://dx.doi.org/10.29289/259453942022v32s1019.
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