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小鼠肥大细胞蛋白酶5基因在源自突变型mi/mi小鼠的培养肥大细胞中的异常表达。

Abnormal expression of mouse mast cell protease 5 gene in cultured mast cells derived from mutant mi/mi mice.

作者信息

Morii E, Jippo T, Tsujimura T, Hashimoto K, Kim D K, Lee Y M, Ogihara H, Tsujino K, Kim H M, Kitamura Y

机构信息

Department of Pathology, Osaka University Medical School, Suita, Japan.

出版信息

Blood. 1997 Oct 15;90(8):3057-66.

PMID:9376586
Abstract

Mast cells contain a lot of mast cell-specific proteases. We have reported that the expression of mouse mast cell protease 6 (MMCP-6) is remarkably reduced in both cultured mast cells (CMCs) and skin mast cells of mi/mi mutant mice. In the present study, we found that the expression of MMCP-5 was reduced in CMCs but not in skin mast cells of mi/mi mice, and we compared the regulation mechanisms of MMCP-5 with those of MMCP-6. The mi locus encodes a member of the basic-helix-loop-helix-leucine zipper (bHLH-Zip) protein family of transcription factors (hereafter called MITF). The consensus sequence recognized and bound by bHLH-Zip transcription factors is CANNTG. The overexpression of the normal (+) MITF but not of mi-MITF normalized the poor expression of the MMCP-5 gene in mi/mi CMCs, indicating the involvement of +-MITF in transactivation of the MMCP-5 gene. Although +-MITF directly bound CANNTG motifs in the promoter region of the MMCP-6 gene and transactivated it, the binding of +-MITF to the CAGTTG motif in the promoter region of the MMCP-5 gene was not detectable. The +-MITF appeared to regulate the transactivation of the MMCP-5 gene indirectly. Moreover, addition of stem cell factor to the medium normalized the expression of the MMCP-5 but not of the MMCP-6 gene in mi/mi CMCs. Despite the significant reduction of both MMCP-5 and MMCP-6 expressions in mi/mi CMCs, their regulation mechanisms appeared to be different.

摘要

肥大细胞含有大量肥大细胞特异性蛋白酶。我们曾报道,在mi/mi突变小鼠的培养肥大细胞(CMC)和皮肤肥大细胞中,小鼠肥大细胞蛋白酶6(MMCP - 6)的表达显著降低。在本研究中,我们发现mi/mi小鼠的CMC中MMCP - 5的表达降低,但皮肤肥大细胞中未降低,并且我们比较了MMCP - 5和MMCP - 6的调控机制。mi基因座编码一种转录因子的碱性螺旋-环-螺旋-亮氨酸拉链(bHLH - Zip)蛋白家族成员(以下称为MITF)。bHLH - Zip转录因子识别并结合的共有序列是CANNTG。正常(+)MITF的过表达而非mi - MITF的过表达使mi/mi CMC中MMCP - 5基因的低表达恢复正常,表明+ - MITF参与了MMCP - 5基因的反式激活。尽管+ - MITF直接结合MMCP - 6基因启动子区域的CANNTG基序并使其反式激活,但未检测到+ - MITF与MMCP - 5基因启动子区域的CAGTTG基序结合。+ - MITF似乎间接调节MMCP - 5基因的反式激活。此外,向培养基中添加干细胞因子可使mi/mi CMC中MMCP - 5的表达恢复正常,但不能使MMCP - 6基因的表达恢复正常。尽管mi/mi CMC中MMCP - 5和MMCP - 6的表达均显著降低,但它们的调控机制似乎不同。

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