Cohen M, Wuillemin C, Irion O, Bischof P
Department of Obstetrics and Gynaecology, Laboratory of Hormonology, University of Geneva, Geneva, Switzerland.
Hum Reprod. 2008 Oct;23(10):2273-81. doi: 10.1093/humrep/den264. Epub 2008 Jul 16.
The matrix metalloproteinase (MMP) family is known to play a key role in tissue remodelling during embryonic development and in pathological conditions, such as cardiovascular disease, arthritis and cancer metastasis. It has been shown previously that p53 regulates positively or negatively the expression of different MMPs. Because of p53 overexpression in trophoblastic cells, and its potential role in regulating MMP-2 and MMP-9 expression in different cell lines, we hypothesized that the expression of MMP-9 could also be regulated by p53 in first trimester cytotrophoblasts (CTB).
Transfection experiments in CTB demonstrated that wild-type p53 down-regulates the -670 (P < 0.001) but not the -531 and -90 human MMP-9 promoter/CAT reporter plasmid activity, whereas p53 mutants partially lost this repressive activity. However, endogenous p53 is not able to regulate MMP-9 expression in CTB. The presence of high molecular weight complexes of p53 in CTB suggests a potential mechanism of inactivation of p53 transcriptional activity towards MMPs in these cells.
Although p53 is mutated in trophoblast, it is functionally incompetent towards MMPs in these cells.
已知基质金属蛋白酶(MMP)家族在胚胎发育过程中的组织重塑以及心血管疾病、关节炎和癌症转移等病理状况中起关键作用。先前已表明,p53对不同MMP的表达具有正向或负向调节作用。鉴于滋养层细胞中p53过表达,以及其在调节不同细胞系中MMP - 2和MMP - 9表达方面的潜在作用,我们推测MMP - 9的表达在孕早期细胞滋养层(CTB)中也可能受p53调节。
CTB中的转染实验表明,野生型p53可下调 - 670(P < 0.001)但不能下调 - 531和 - 90人MMP - 9启动子/氯霉素乙酰转移酶(CAT)报告质粒活性,而p53突变体部分丧失了这种抑制活性。然而,内源性p53无法调节CTB中MMP - 9的表达。CTB中存在p53的高分子量复合物,提示这些细胞中p53对MMPs转录活性失活的潜在机制。
尽管滋养层中p53发生了突变,但它在这些细胞中对MMPs功能上无活性。