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淋巴细胞功能相关抗原-1(LFA-1)和p150,95白细胞整合素表达的调控:CD11a和CD11c基因启动子的作用

Regulation of expression of the LFA-1 and p150,95 leukocyte integrins: involvement of the CD11a and CD11c gene promoters.

作者信息

López-Rodríguez C, Nueda A, Rubio M, Corbí A L

机构信息

Hospital de la Princesa, Madrid, Spain.

出版信息

Immunobiology. 1995 Jul;193(2-4):315-21. doi: 10.1016/s0171-2985(11)80560-7.

Abstract

Human Lymphocyte Associated Antigen-1 (LFA-1, CD11a/CD18, alpha L/beta 2) and p150,95 (CD11c/CD18, alpha X/beta 2) are cell surface alpha/beta heterodimers that, together with Mac-1 (CD11b/CD18, alpha M/beta 2) comprise the leukocyte-restricted beta 2 subfamily of integrins. LFA-1 is the only integrin expressed on all leukocyte lineages while p150,95 is exclusively expressed on cells of the myeloid lineage and on activated B lymphocytes and natural killer cells. The expression of the leukocyte integrins is regulated during cell activation and differentiation by transcriptional mechanisms. To dissect the molecular basis for the tissue-restricted and developmentally regulated expression of LFA-1 and p150,95, the promoter regions of their corresponding alpha subunits (CD11a and CD11c) were isolated and functionally characterized. Both promoters lack TATA and CAAT boxes, but exhibit initiator-like sequences at their major transcriptional start sites. Transient expression of CD11a- and CD11c-based reporter gene constructs have demonstrated the involvement of both promoters in the tissue-specific expression of LFA-1 and p150,95. Furthermore, a combination of DNAse I protection experiments and mobility band shift assays have revealed the existence of numerous DNA-protein interactions at the proximal region of both promoters, some of which overlap with consensus binding sequences for known transcription factors and correlate with the pattern of expression of both integrins.

摘要

人类淋巴细胞相关抗原-1(LFA-1,CD11a/CD18,αL/β2)和p150,95(CD11c/CD18,αX/β2)是细胞表面的α/β异二聚体,它们与Mac-1(CD11b/CD18,αM/β2)共同构成整合素的白细胞限制性β2亚家族。LFA-1是所有白细胞谱系中唯一表达的整合素,而p150,95仅在髓系谱系细胞、活化的B淋巴细胞和自然杀伤细胞上表达。白细胞整合素的表达在细胞活化和分化过程中受转录机制调控。为了剖析LFA-1和p150,95组织限制性和发育调控性表达的分子基础,分离了它们相应α亚基(CD11a和CD11c)的启动子区域并进行了功能表征。两个启动子均缺乏TATA盒和CAAT盒,但在其主要转录起始位点显示出类似起始子的序列。基于CD11a和CD11c的报告基因构建体的瞬时表达证明了两个启动子均参与LFA-1和p150,95的组织特异性表达。此外,DNA酶I保护实验和迁移率带移分析相结合揭示了两个启动子近端区域存在大量DNA-蛋白质相互作用,其中一些与已知转录因子的共有结合序列重叠,并与两种整合素的表达模式相关。

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