期刊
CELL CYCLE
卷 13, 期 2, 页码 324-333出版社
TAYLOR & FRANCIS INC
DOI: 10.4161/cc.27118
关键词
BMP2/4; Noggin; BMPRIA; Alk3; Smad; thymus; DN thymocyte; DP; differentiation; T-cell development
类别
资金
- Royal Society
- Wellcome Trust
- BBSRC
- MRC
- CHRAT
- Asthma UK
- Great Ormond Street Hospital Children's Charity
- BBSRC [BB/H005188/1, BB/I026324/1] Funding Source: UKRI
- MRC [G0900161] Funding Source: UKRI
- Asthma UK [AUK-SPD-2012-171] Funding Source: researchfish
- Biotechnology and Biological Sciences Research Council [BB/H005188/1, BB/I026324/1] Funding Source: researchfish
- Great Ormond Street Hospital Childrens Charity [V1297] Funding Source: researchfish
- Medical Research Council [G0900161] Funding Source: researchfish
BMP2/4 signaling is required for embryogenesis and involved in thymus morphogenesis and T-lineage differentiation. In vitro experiments have shown that treatment of thymus explants with exogenous BMP4 negatively regulated differentiation of early thymocyte progenitors and the transition from CD4-CD8- (DN) to CD4+CD8+ (DP). Here we show that in vivo BMP2/4 signaling is required for fetal thymocyte progenitor homeostasis and expansion, but negatively regulates differentiation from DN to DP cell. Unexpectedly, conditional deletion of BMPRIA from fetal thymocytes (using the Cre-loxP system and directing excision to hematopoietic lineage cells with the Vav promoter) demonstrated that physiological levels of BMP2/4 signaling directly to thymocytes through BMPRIA are required for normal differentiation and expansion of early fetal DN thymocytes. In contrast, the arrest in early thymocyte progenitor differentiation caused by exogenous BMP4 treatment of thymus explants is induced in part by direct signaling to thymocytes through BMPRIA, and in part by indirect signaling through non-hematopoietic cells. Analysis of the transition from fetal DN to DP cell, both by ex vivo analysis of conditional BMPRIA-deficient thymocytes and by treatment of thymus explants with the BMP4-inhibitor Noggin demonstrated that BMP2/4 signaling is a negative regulator at this stage. We showed that at this stage of fetal T-cell development BMP2/4 signals directly to thymocytes through BMPRIA.
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