Regulation of B-cell development and tolerance by different members of the miR-17∼92 family microRNAs

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作者
Maoyi Lai
Alicia Gonzalez-Martin
Anthony B. Cooper
Hiroyo Oda
Hyun Yong Jin
Jovan Shepherd
Linling He
Jiang Zhu
David Nemazee
Changchun Xiao
机构
[1] The Scripps Research Institute,Department of Immunology and Microbial Science
[2] Kellogg School of Science and Technology,undefined
[3] The Scripps Research Institute,undefined
[4] Present address: Adimab,undefined
[5] 7 Lucent Drive,undefined
[6] Lebanon,undefined
[7] New Hampshire 03766,undefined
[8] USA,undefined
[9] Present address: Department of Immunology and Pathology,undefined
[10] Research Institute,undefined
[11] National Center for Global Health and Medicine,undefined
[12] 1-7-1,undefined
[13] Konodai,undefined
[14] Ichikawa-shi,undefined
[15] Chiba 272-8516,undefined
[16] Japan,undefined
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摘要
The molecular mechanisms that regulate B-cell development and tolerance remain incompletely understood. In this study, we identify a critical role for the miR-17∼92 microRNA cluster in regulating B-cell central tolerance and demonstrate that these miRNAs control early B-cell development in a cell-intrinsic manner. While the cluster member miR-19 suppresses the expression of Pten and plays a key role in regulating B-cell tolerance, miR-17 controls early B-cell development through other molecular pathways. These findings demonstrate differential control of two closely linked B-cell developmental stages by different members of a single microRNA cluster through distinct molecular pathways.
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