Requirement for B Cell Linker Protein (BLNK) in B Cell Development
- 3 December 1999
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 286 (5446), 1949-1954
- https://doi.org/10.1126/science.286.5446.1949
Abstract
Linker proteins function as molecular scaffolds to localize enzymes with substrates. In B cells, B cell linker protein (BLNK) links the B cell receptor (BCR)–activated Syk kinase to the phosphoinositide and mitogen-activated kinase pathways. To examine the in vivo role of BLNK, mice deficient in BLNK were generated. B cell development in BLNK −/− mice was blocked at the transition from B220+CD43+ progenitor B to B220+CD43− precursor B cells. Only a small percentage of immunoglobulin M++ (IgM++), but not mature IgMloIgDhi, B cells were detected in the periphery. Hence, BLNK is an essential component of BCR signaling pathways and is required to promote B cell development.Keywords
This publication has 39 references indexed in Scilit:
- Fetal hemorrhage and platelet dysfunction in SLP-76–deficient miceJournal of Clinical Investigation, 1999
- BLNKImmunity, 1998
- Mutations in the Human λ5/14.1 Gene Result in B Cell Deficiency and AgammaglobulinemiaThe Journal of Experimental Medicine, 1998
- bca: an activation-related B-cell geneMolecular Immunology, 1998
- Regulation of B-lymphocyte negative and positive selection by tyrosine phosphatase CD45Nature, 1996
- Perinatal lethality and blocked B-cell development in mice lacking the tyrosine kinase SykNature, 1995
- Defective B cell development and function in Btk-deficient miceImmunity, 1995
- Defective T cell receptor signaling and CD8+ thymic selection in humans lacking Zap-70 kinaseCell, 1994
- Origin of Murine B Cell LineagesAnnual Review of Immunology, 1993
- Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemiaCell, 1993