生发中心
生物
体细胞突变
B细胞
淋巴瘤
基因表达谱
免疫球蛋白轻链
分子生物学
遗传学
癌症研究
细胞生物学
基因
抗体
免疫学
基因表达
作者
Gabriel D. Victora,David Dominguez-Sola,Antony B. Holmes,Stephanie Deroubaix,Riccardo Dalla‐Favera,Michel C. Nussenzweig
出处
期刊:Blood
[American Society of Hematology]
日期:2012-09-13
卷期号:120 (11): 2240-2248
被引量:310
标识
DOI:10.1182/blood-2012-03-415380
摘要
Germinal centers (GCs) are sites of B-cell clonal expansion, hypermutation, and selection. GCs are polarized into dark (DZ) and light zones (LZ), a distinction that is of key importance to GC selection. However, the difference between the B cells in each of these zones in humans remains unclear. We show that, as in mice, CXCR4 and CD83 can be used to distinguish human LZ and DZ cells. Using these markers, we show that LZ and DZ cells in mice and humans differ only in the expression of characteristic "activation" and "proliferation" programs, suggesting that these populations represent alternating states of a single-cell type rather than distinct differentiation stages. In addition, LZ/DZ transcriptional profiling shows that, with the exception of "molecular" Burkitt lymphomas, nearly all human B-cell malignancies closely resemble LZ cells, which has important implications for our understanding of the molecular programs of lymphomagenesis.
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