Characterization of thymic stromal-derived lymphopoietin (TSLP) in murine B cell development in vitro.

Abstract:

:B cell development is dependent on both direct interactions with stromal cells and their secreted cytokines. The precise mechanisms by which these interactions regulate B cell differentiation are currently unknown. We report here that a novel growth factor thymic stromal-derived lymphopoietin (TSLP) can replace the activity of interleukin-7 (IL-7) in supporting B cell development in vitro. TSLP was found to promote the proliferation and differentiation of committed B220+ B cell progenitors from day 15 fetal liver. Phenotypic analysis of these cells revealed that they are at the pro-B cell stage of differentiation and express cell surface markers characteristic of pro-B cells cultured in IL-7. TSLP can replace the activity of IL-7 in supporting the progression of B lymphocytes from uncommitted bipotential precursors. In the absence of either TSLP or IL-7, the progeny of cells that give rise to mature B lymphocytes fail to develop from these bipotential precursors. Moreover, TSLP can substitute for IL-7 in supporting the sustained proliferative response exhibited by B cell progenitors from CBA/N mice. Together these results show that TSLP can replace the requirement for IL-7 during in vitro B cell development.

journal_name

Eur J Immunol

authors

Ray RJ,Furlonger C,Williams DE,Paige CJ

doi

10.1002/eji.1830260103

subject

Has Abstract

pub_date

1996-01-01 00:00:00

pages

10-6

issue

1

eissn

0014-2980

issn

1521-4141

journal_volume

26

pub_type

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