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滋养层细胞在胚胎植入中的作用:旁分泌因子的调控

Involvement of trophoblast in embryo implantation: regulation by paracrine factors.

作者信息

Bischof P, Meisser A, Campana A

机构信息

Clinic of Infertility and Gynaecologic Endocrinology, WHO Collaborating Center for Human Reproduction, Department of Obstetrics and Gynaecology, University of Geneva, Maternité, Switzerland.

出版信息

J Reprod Immunol. 1998 Aug;39(1-2):167-77. doi: 10.1016/s0165-0378(98)00020-5.

Abstract

In order to investigate the regulatory role of only one endometrial cell type on trophoblastic invasion, we explored the effects of culture medium conditioned by in vitro decidualised stromal cells (DCM) and of insulin-like growth factor binding protein-1 (IGFBP-1, the main secretory product of decidual cells) on the trophoblastic secretion of gelatinases and tissue inhibitor of metalloproteinases (TIMP-1). First trimester cytotrophoblastic cells (CTB) were obtained from abortions and cultured in vitro in presence or absence of DCM or IGFBP-1. Secreted gelatinases were analysed in the culture supernatants by zymography and by measurements of the total gelatinolytic activity. Tissue inhibitor of metalloproteinases (TIMP-1) was measured by a commercially available immunoassay. DCM inhibited the total gelatinolytic activity of CTB but increased trophoblastic MMP-9 and TIMP-1. In contrast, IGFBP-1 increased the total gelatinolytic activity and TIMP-1 and had no effect on MMP-2 and MMP-9. We conclude that a factor secreted by decidual cells (possibly TGFbeta) inhibits the total gelatinolytic activity of trophoblast by increasing TIMP-1 but other factors, as yet unidentified, increase MMP-2 and MMP-9 to an extent which does not shift the equilibrium between the gelatinases and TIMP-1 in favour of the gelatinases. In contrast to DCM, IGFBP-1 increases the total gelatinolytic activity probably by stimulating another gelatinase (stromelysin-1?) as MMP-2 and MMP 9 are unchanged by IGFBP-1. The possibility of an integrin mediated effect of IGFBP-1 on CTB is discussed.

摘要

为了研究仅一种子宫内膜细胞类型对滋养层细胞侵袭的调节作用,我们探讨了体外蜕膜化基质细胞(DCM)条件培养基以及胰岛素样生长因子结合蛋白-1(IGFBP-1,蜕膜细胞的主要分泌产物)对滋养层细胞明胶酶和金属蛋白酶组织抑制剂(TIMP-1)分泌的影响。从人工流产中获取孕早期细胞滋养层细胞(CTB),并在有或无DCM或IGFBP-1的情况下进行体外培养。通过酶谱分析和总明胶酶活性测量来分析培养上清液中分泌的明胶酶。通过市售免疫测定法测量金属蛋白酶组织抑制剂(TIMP-1)。DCM抑制CTB的总明胶酶活性,但增加滋养层细胞的MMP-9和TIMP-1。相反,IGFBP-1增加总明胶酶活性和TIMP-1,并且对MMP-2和MMP-9没有影响。我们得出结论,蜕膜细胞分泌的一种因子(可能是TGFβ)通过增加TIMP-1来抑制滋养层细胞的总明胶酶活性,但其他尚未确定的因子会增加MMP-2和MMP-9,其程度不会使明胶酶和TIMP-1之间的平衡向有利于明胶酶的方向转变。与DCM相反,IGFBP-1可能通过刺激另一种明胶酶(基质溶解素-1?)来增加总明胶酶活性,因为IGFBP-1对MMP-2和MMP 9没有影响。讨论了IGFBP-1对CTB的整合素介导作用的可能性。

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