期刊
NATURE
卷 516, 期 7530, 页码 254-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature13765
关键词
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资金
- Leukemia & Lymphoma Society
- National Institutes of Health (NIH) [T32 DK007636, T32 CA1285835]
- Dr Mildred Scheel Stiftung fur Krebsforschung (Deutsche Krebshilfe)
- NIH [GM097261, AI45073]
- Lymphoma/Leukemia Molecular Profiling Project
- NIH, National Cancer Institute, Center for Cancer Research
Germinal centre B-cell-like diffuse large B-cell lymphoma(GCB-DLBCL) is a common malignancy, yet the signalling pathways that are deregulated and the factors leading to its systemic dissemination are poorly defined(1,2). Work in mice showed that sphingosine-1-phosphate receptor-2 (S1PR2), a G alpha 12 and G alpha 13 coupled receptor, promotes growth regulation and local confinement of germinal centre B cells(3,4). Recent deep sequencing studies of GCB-DLBCL have revealed mutations in many genes in this cancer, including in GNA13 (encoding G alpha 13) and S1PR2 (refs 5-7). Here we show, using in vitro and in vivo assays, that GCB-DLBCL-associated mutations occurring in S1PR2 frequently disrupt the receptor's Akt and migration inhibitory functions. G alpha 13-deficient mouse germinal centre B cells and human GCB-DLBCL cells were unable to suppress pAkt and migration in response to S1P, and G alpha 13-deficient mice developed germinal centre B-cell-derived lymphoma. Germinal centre B cells, unlike most lymphocytes, are tightly confined in lymphoid organs and do not recirculate. Remarkably, deficiency in G alpha 13, but not S1PR2, led to germinal centre B-cell dissemination into lymph and blood. GCB-DLBCL cell lines frequently carried mutations in the G alpha 13 effector ARHGEF1, and Arhgef1 deficiency also led to germinal centre B-cell dissemination. The incomplete phenocopy of G alpha 13- and S1PR2 deficiency led us to discover that P2RY8, an orphan receptor that is mutated in GCB-DLBCL and another germinal centre B-cell-derived malignancy, Burkitt's lymphoma, also represses germinal centre B-cell growth and promotes confinement via G alpha 13. These findings identify a G alpha 13-dependent pathway that exerts dual actions in suppressing growth and blocking dissemination of germinal centre B cells that is frequently disrupted in germinal centre B-cell-derived lymphoma.
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