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Publication : Differential requirement for p56lck in fetal and adult thymopoiesis.

First Author  Molina TJ Year  1998
Journal  J Immunol Volume  160
Issue  8 Pages  3828-34
PubMed ID  9558087 Mgi Jnum  J:47242
Mgi Id  MGI:1202827 Doi  10.4049/jimmunol.160.8.3828
Citation  Molina TJ, et al. (1998) Differential requirement for p56lck in fetal and adult thymopoiesis. J Immunol 160(8):3828-34
abstractText  The protein tyrosine kinase p56lck is critical for the generation of mature thymocytes in adult mice. However its requirement during the maturation of thymocytes from the fetal to the adult stage has not been clearly defined. We analyzed prenatal and postnatal thymocyte maturation in mice deficient for p56lck (lck[-/-]). Before birth, lck appears to play a crucial role in the expansion and proliferation of CD4+CD8+ double positive thymocytes, whereas proliferation and absolute numbers of CD4-CD8- double negative thymocyte precursors remained within the normal range until the end of the second week postnatal. Three weeks after birth, the total numbers of double negative and immature single positive thymocytes underwent a dramatic reduction that correlated with a decrease in the double positive population. This ontogenic defect was associated with a significant decrease in the proliferation rates of thymocyte precursors. Our data suggest that signaling via p56lck kinase is differentially required within a given phenotypically defined thymocyte subpopulation, depending on its stage of thymocyte maturation.
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