 |
Journal articles
Fas receptor signaling is requisite for B cell differentiation
Abstract : The Fas/Fas ligand (FasL) pathway has been largely implicated in the homeostasis of mature cells. However, it is still unclear whether it plays a role at the progenitor level. To address this issue, we created chimeric mice by transferring C57BL/6 bone marrow (BM) cells of the lpr (Fas−FasL+) or gld (Fas+FasL−) genotype into Rag‐2−/− hosts of the same genetic background. In this model, the consequences of a deficient Fas/FasL pathway on lymphoid differentiation could be evaluated without endogenous competition. Analysis of the chimerism revealed a differential sensitivity of hematopoietic lineages to the lack of Fas receptor signaling. While donor‐derived myelo‐monocytic cells were similarly distributed in all chimeric mice, mature B cells were deleted in the BM and the spleen of lpr chimera, leading to the absence of the marginal zone (MZ) as detected by immunohistology. In contrast, B cell hematopoiesis was complete in gld chimera but MZ macrophages undetectable. These defects suggest a direct and determinant dual role of FasL regulation in negative selection of B cells and in maintenance of the MZ.
https://hal-univ-paris.archives-ouvertes.fr/hal-01996498
Contributor : Administrateur Hal Descartes Connect in order to contact the contributor
Submitted on : Monday, January 28, 2019 - 2:24:00 PM
Last modification on : Wednesday, October 14, 2020 - 4:13:20 AM
Contributor : Administrateur Hal Descartes Connect in order to contact the contributor
Submitted on : Monday, January 28, 2019 - 2:24:00 PM
Last modification on : Wednesday, October 14, 2020 - 4:13:20 AM