PLCγ-dependent mTOR signalling controls IL-7-mediated early B cell development View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-12

AUTHORS

Mei Yu, Yuhong Chen, Hu Zeng, Yongwei Zheng, Guoping Fu, Wen Zhu, Ulrich Broeckel, Praful Aggarwal, Amy Turner, Geoffrey Neale, Cliff Guy, Nan Zhu, Hongbo Chi, Renren Wen, Demin Wang

ABSTRACT

The precise molecular mechanism underlying the regulation of early B cell lymphopoiesis is unclear. The PLCγ signaling pathway is critical for antigen receptor-mediated lymphocyte activation, but its function in cytokine signaling is unknown. Here we show that PLCγ1/PLCγ2 double deficiency in mice blocks early B cell development at the pre-pro-B cell stage and renders B cell progenitors unresponsive to IL-7. PLCγ pathway inhibition blocks IL-7-induced activation of mTOR, but not Stat5. The PLCγ pathway activates mTOR through the DAG/PKC signaling branch, independent of the conventional Akt/TSC/Rheb signaling axis. Inhibition of PLCγ/PKC-induced mTOR activation impairs IL-7-mediated B cell development. PLCγ1/PLCγ2 double-deficient B cell progenitors have reduced expression of genes related to B cell lineage, IL-7 signaling, and cell cycle. Thus, IL-7 receptor controls early B lymphopoiesis through activation of mTOR via PLCγ/DAG/PKC signaling, not via Akt/Rheb signaling. More... »

PAGES

1457

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41467-017-01388-5

DOI

http://dx.doi.org/10.1038/s41467-017-01388-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1092580935

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/29133930


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459 Blood Research Institute, Blood Center of Wisconsin, 53226, Milwaukee, WI, USA
460 Department of Microbiology and Molecular Genetics, Medical College of Wisconsin, 53226, Milwaukee, WI, USA
461 Section of Genomic Pediatrics, Department of Pediatrics, Medical College of Wisconsin, 53226, Milwaukee, WI, USA
462 rdf:type schema:Organization
 




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