Molecular Mechanisms Controlling Guided Germ Cell Migration in Zebrafish

作者: Bijan Boldajipour

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摘要: During zebrafish embryonic development, primordial germ cells (PGCs) migrate through the developing embryo towards gonad, where they will differentiate into sperm and egg. their migration, these are guided by chemokine CXCL12a its receptor CXCR4b. Dynamic cxcl12a expression lays out a chemotactic path, remain in immediate proximity to secreting chemokine. This implies that protein level is highest at site of mRNA expression, yet little known about molecular mechanisms controlling distribution this chemoattractant vivo. work demonstrates activity second receptor, CXCR7, crucial for proper migration PGCs toward targets. It shown CXCR7 expressed somatic environment rather than within migrating PGCs. Upon loss function, exhibit phenotype signifies defects gradient formation, as fail polarize effectively Indeed, expressing show enhanced internalization suggesting acts decoy CXCL12a; thus, allowing dynamic changes transcription be mirrored similar dynamics level. In addition guidance CXCL12a, paralog CXCL12 termed CXCL12b during development. not required cell gonads, but capable attracting Although being time ignored long present. sets identify mechanism employ between very ligands identified an amino acid 30 s loop chemokines responsible differential activity. To end, recombinant production established structure, binding vivo, glycosaminoglycan vitro investigated. experiments still progress, it appears single controls activation, whereas glycosaminoglycans affected.

参考文章(220)
Thomas Brabletz, Andreas Jung, Simone Spaderna, Falk Hlubek, Thomas Kirchner, Migrating cancer stem cells — an integrated concept of malignant tumour progression Nature Reviews Cancer. ,vol. 5, pp. 744- 749 ,(2005) , 10.1038/NRC1694
Mark Van Doren, Heather Tarczy Broihier, Lisa A Moore, Ruth Lehmann, None, HMG-CoA reductase guides migrating primordial germ cells Nature. ,vol. 396, pp. 466- 469 ,(1998) , 10.1038/24871
G. D'Amico, G. Frascaroli, G. Bianchi, P. Transidico, A. Doni, A. Vecchi, S. Sozzani, P. Allavena, A. Mantovani, Uncoupling of inflammatory chemokine receptors by IL-10: generation of functional decoys Nature Immunology. ,vol. 1, pp. 387- 391 ,(2000) , 10.1038/80819
Anthony J. Pelletier, Luc J. W. van der Laan, Patrick Hildbrand, Michael A. Siani, Darren A. Thompson, Philip E. Dawson, Bruce E. Torbett, Daniel R. Salomon, Presentation of chemokine SDF-1α by fibronectin mediates directed migration of T cells Blood. ,vol. 96, pp. 2682- 2690 ,(2000) , 10.1182/BLOOD.V96.8.2682
Zhongbin Bai, Haruko Hayasaka, Masayoshi Kobayashi, Wenzhe Li, Zijin Guo, Myoung Ho Jang, Akihiro Kondo, Byung-il Choi, Yoichiro Iwakura, Masayuki Miyasaka, CXC Chemokine Ligand 12 Promotes CCR7-Dependent Naive T Cell Trafficking to Lymph Nodes and Peyer’s Patches Journal of Immunology. ,vol. 182, pp. 1287- 1295 ,(2009) , 10.4049/JIMMUNOL.182.3.1287
Robert R. Kay, Paul Langridge, David Traynor, Oliver Hoeller, Changing directions in the study of chemotaxis. Nature Reviews Molecular Cell Biology. ,vol. 9, pp. 455- 463 ,(2008) , 10.1038/NRM2419
Douglas W. Houston, Mary Lou King, Germ plasm and molecular determinants of germ cell fate. Current Topics in Developmental Biology. ,vol. 50, pp. 155- 181 ,(2000) , 10.1016/S0070-2153(00)50008-8
B. Moser, B. Dewald, L. Barella, C. Schumacher, M. Baggiolini, I. Clark-Lewis, Interleukin-8 antagonists generated by N-terminal modification. Journal of Biological Chemistry. ,vol. 268, pp. 7125- 7128 ,(1993) , 10.1016/S0021-9258(18)53154-9
Matthew P Crump, Elena Elisseeva, Jiang-Hong Gong, Ian Clark-Lewis, Brian D Sykes, Structure/function of human herpesvirus-8 MIP-II (1-71) and the antagonist N-terminal segment (1-10). FEBS Letters. ,vol. 489, pp. 171- 175 ,(2001) , 10.1016/S0014-5793(00)02393-0