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首页> 外文期刊>Molecular human reproduction. >Dynamic expression of mRNAs and proteins for matrix metalloproteinases and their tissue inhibitors in the primate corpus luteum during the menstrual cycle.
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Dynamic expression of mRNAs and proteins for matrix metalloproteinases and their tissue inhibitors in the primate corpus luteum during the menstrual cycle.

机译:月经周期灵长类动物黄体中基质金属蛋白酶及其组织抑制剂的mRNA和蛋白的动态表达。

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Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) may be involved in tissue remodelling in the primate corpus luteum (CL). MMP/TIMP mRNA and protein patterns were examined using real-time PCR and immunohistochemistry in the early, mid-, mid-late, late and very late CL of rhesus monkeys. MMP-1 (interstitial collagenase) mRNA expression peaked (by >7-fold) in the early CL. MMP-9 (gelatinase B) mRNA expression was low in the early CL, but increased 41-fold by the very late stage. MMP-2 (gelatinase A) mRNA expression tended to increase in late CL. TIMP-1 mRNA was highly expressed in the CL, until declining 21-fold by the very late stage. TIMP-2 mRNA expression was high through the mid-luteal phase. MMP-1 protein was detected by immunocytochemistry in early steroidogenic cells. MMP-2 protein was prominent in late, but not early CL microvasculature. MMP-9 protein was noted in early CL and labelling increased in later stage steroidogenic cells. TIMP-1 and -2 proteins were detected in steroidogenic cells at all stages. Thus, MMPs and TIMPs are dynamically expressed in a cell-specific manner in the primate CL. Early expression of MMP-1 is suggestive of a role in tissue remodelling associated with luteinization, whereas MMP-2 and -9 may contribute to later stage luteolysis. TIMP expression may control MMP activity, until declining at luteolysis.
机译:基质金属蛋白酶(MMPs)及其组织抑制剂(TIMPs)可能参与黄体灵长类动物(CL)的组织重塑。使用实时PCR和免疫组织化学技术在恒河猴的早期,中晚期,中晚期,晚期和非常晚期的CL中检查了MMP / TIMP mRNA和蛋白质模式。在早期CL中,MMP-1(间质胶原酶)mRNA表达达到峰值(> 7倍)。在早期CL中,MMP-9(明胶酶B)mRNA表达较低,但到晚期时,其表达增加了41倍。在CL晚期,MMP-2(明胶酶A)mRNA表达趋于增加。 TIMP-1 mRNA在CL中高表达,直到很晚才下降21倍。在黄体中期,TIMP-2 mRNA的表达较高。通过免疫细胞化学在早期类固醇生成细胞中检测到MMP-1蛋白。 MMP-2蛋白在CL微脉管系统晚期但未在CL微血管系统中突出。在早期CL中注意到MMP-9蛋白,并且在晚期类固醇生成细胞中标记增加。在所有阶段的类固醇生成细胞中均检测到TIMP-1和-2蛋白。因此,在灵长类CL中以细胞特异性方式动态表达MMP和TIMP。 MMP-1的早期表达提示与黄体化相关的组织重塑,而MMP-2和-9可能有助于后期黄体溶解。 TIMP表达可能控制MMP活性,直到黄体溶解下降为止。

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