Thymic stromal lymphopoietin: a cytokine that promotes the development of IgM+ B cells in vitro and signals via a novel mechanism
Autor: | S D, Levin, R M, Koelling, S L, Friend, D E, Isaksen, S F, Ziegler, R M, Perlmutter, A G, Farr |
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Rok vydání: | 1999 |
Předmět: |
Time Factors
B-Lymphocyte Subsets Bone Marrow Cells Thymus Gland Cell Line Colony-Forming Units Assay Mice Fetus Thymic Stromal Lymphopoietin Proto-Oncogene Proteins STAT5 Transcription Factor Animals Phosphorylation Cells Cultured Receptors Interleukin-7 Interleukin-7 Janus Kinase 3 Cell Differentiation Janus Kinase 1 Janus Kinase 2 Protein-Tyrosine Kinases Milk Proteins DNA-Binding Proteins Enzyme Activation Immunoglobulin M Liver Trans-Activators Cytokines Tyrosine Stromal Cells Signal Transduction |
Zdroj: | Journal of immunology (Baltimore, Md. : 1950). 162(2) |
ISSN: | 0022-1767 |
Popis: | A novel cytokine from a thymic stromal cell line (thymic stromal lymphopoietin (TSLP)) promotes the development of B220+/IgM+ immature B cells when added to fetal liver cultures, long term bone marrow cultures, or bone marrow cells plated in semisolid medium. Because the activities of TSLP overlap with those of IL-7 in some in vitro assays, we compared the signaling mechanisms employed by TSLP and IL-7. Proliferation of a factor-dependent pre-B cell line (NAG8/7) in response to either TSLP or IL-7 was inhibited by anti-IL-7R alpha mAbs, suggesting that the functional TSLP receptor complex uses IL-7R alpha. In contrast, three different Abs to the common cytokine receptor gamma-chain had no effect on the response of these cells to TSLP, indicating that the functional TSLP receptor complex does not use the common cytokine receptor gamma-chain. Both cytokines induced activation of Stat5, but only IL-7 induced activation of the Janus family kinases Jak1 and Jak3. In fact, TSLP failed to activate any of the four known Janus family kinases, suggesting that Stat5 phosphorylation is mediated by a novel mechanism. Taken together, these data support the idea that TSLP can make unique contributions to B lymphopoiesis and indicate that it does so by mechanisms distinct from IL-7. |
Databáze: | OpenAIRE |
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