CXC chemokine ligand 13 and CC chemokine ligand 19 cooperatively render resistance to apoptosis in B cell lineage acute and chronic lymphocytic leukemia CD23(+)CD5(+) B cells | |
Hu, CS; He, YL; Wang, L; Xiong, J; Zhou, G; Zhang, QP; Gao, QP; Zhang, KJ; Qiao, L; Chang, AE | |
刊名 | JOURNAL OF IMMUNOLOGY
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2006 | |
卷号 | 177期号:10页码:6713-6722 |
通讯作者 | Tan, JQ (reprint author), Anhui Med Univ, Dept Immunol, Sch Basic Med Sci, Hefei 230032, Peoples R China.,jinquan_tan@hotmai.com |
英文摘要 | CXCL13/CXCR5 and CCL19/CCR7 play a quite important role in normal physiological conditions, but the functions of both chemokine/receptor pairs in pathophysiological events are not well-investigated. We have investigated expression and functions of CXCL13/CXCR5 and CCL19/CCR7 in CD23(+)CD5(+) and CD23(+)CD5(-) B cells from cord blood (CB) and patients with B cell linea-e acute or chronic lymphocytic leukemia (B-ALL or B-CLL). CXCR5 and CCR7 are selectively expressed on B-ALL, B-CLL, and CB CD23(+)CD5(+) B cells at high frequency, but not on CD23+CD5- B cells. Although no significant chemotactic responsiveness was observed, CXCL13 and CCL19 cooperatively induce significant resistance to TNF-alpha-mediated apoptosis in B-ALL and B-CLL CD23(+)CD5(+) B cells, but not in the cells from CB. B-ALL and B-CLL CD23(+)CD5(+) B cells express elevated levels of paternally expressed gene 10 (PEG10). CXCL13 and CCL19 together significantly up-regulate PEG10 expression in the same cells. We have found that CXCL13 and CCL19 together by means of activation of CXCR5 and CCR7 up-regulate PEG10 expression and function, subsequently stabilize caspase-3 and caspase-8 in B-ALL and B-CLL CD23(+)CD5(+) B cells, and further rescue the cells from TNF-a-mediated apoptosis. Therefore, we suggest that normal lymphocytes, especially naive B and T cells, use CXCL13/CXCR5 and CCL19/CCR7 for migration, homing, maturation, and cell homeostasis as well as secondary lymphoid tissues organogenesis. In addition, certain malignant cells take advantages of CXCL13/CXCR5 and CCL19/CCR7 for infiltration, resistance to apoptosis, and inappropriate proliferation. |
学科主题 | Immunology |
类目[WOS] | Immunology |
关键词[WOS] | RECEPTOR 9/TECK INTERACTION ; LYMPH-NODES ; DENDRITIC CELLS ; T-LYMPHOCYTES ; MIGRATION ; EXPRESSION ; GENE ; PEG10 ; ACTIVATION ; FOLLICLES |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000242009700019 |
内容类型 | 期刊论文 |
版本 | 出版稿 |
源URL | [http://202.127.25.143/handle/331003/1765] ![]() |
专题 | 上海生化细胞研究所_上海生科院生化细胞研究所 |
推荐引用方式 GB/T 7714 | Hu, CS,He, YL,Wang, L,et al. CXC chemokine ligand 13 and CC chemokine ligand 19 cooperatively render resistance to apoptosis in B cell lineage acute and chronic lymphocytic leukemia CD23(+)CD5(+) B cells[J]. JOURNAL OF IMMUNOLOGY,2006,177(10):6713-6722. |
APA | Hu, CS.,He, YL.,Wang, L.,Xiong, J.,Zhou, G.,...&Tan, JQ.(2006).CXC chemokine ligand 13 and CC chemokine ligand 19 cooperatively render resistance to apoptosis in B cell lineage acute and chronic lymphocytic leukemia CD23(+)CD5(+) B cells.JOURNAL OF IMMUNOLOGY,177(10),6713-6722. |
MLA | Hu, CS,et al."CXC chemokine ligand 13 and CC chemokine ligand 19 cooperatively render resistance to apoptosis in B cell lineage acute and chronic lymphocytic leukemia CD23(+)CD5(+) B cells".JOURNAL OF IMMUNOLOGY 177.10(2006):6713-6722. |
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