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小鼠植入前囊胚粘附于表达跨膜形式肝素结合表皮生长因子样生长因子的细胞。

Mouse preimplantation blastocysts adhere to cells expressing the transmembrane form of heparin-binding EGF-like growth factor.

作者信息

Raab G, Kover K, Paria B C, Dey S K, Ezzell R M, Klagsbrun M

机构信息

Department of Surgery, Children's Hospital and Harvard Medical School, Boston, MA 02115, USA.

出版信息

Development. 1996 Feb;122(2):637-45. doi: 10.1242/dev.122.2.637.

Abstract

Previous studies have shown that heparin-binding epidermal growth factor (EGF)-like growth factor (HB-EGF) mRNA is synthesized in the mouse uterine luminal epithelium temporally, just prior to implantation, and spatially, only at the site of blastocyst apposition (Das, S. K., Wang, X. N., Paria, B. C., Damm, D., Abraham, J. A., Klagsbrun, M., Andrews, G. K. and Dey, S. K. (1994) Development 120, 1071-1083). HB-EGF is synthesized as a transmembrane protein (HB-EGF TM) that can be processed to release the soluble growth factor. An antibody that cross-reacts only with the transmembrane form detected HB-EGF TM in uterine luminal epithelium in a spatial manner similar to that of HB-EGF mRNA. HB-EGF TM is a juxtacrine growth factor that mediates cell-cell contact. To ascertain if HB-EGF TM could be an adhesion factor for blastocysts, a mouse cell line synthesizing human HB-EGF TM was co-cultured with mouse blastocysts. Cells synthesizing HB-EGF TM adhered to day-4 mouse blastocysts more extensively than parental cells or cells synthesizing a constitutively secreted form of HB-EGF. Adhesion of cells synthesizing HB-EGF TM to blastocysts was inhibited by excess recombinant HB-EGF but less so by TGF-alpha. Adhesion was also inhibited by the synthetic peptide P21 corresponding to the HB-EGF heparin binding domain, and by incubating the blastocysts with heparinase. In addition, adhesion to delayed implanting dormant blastocysts, which lack EGF receptor (EGFR), was diminished relative to normal blastocysts. These results suggested that adhesion between blastocysts and cells synthesizing HB-EGF TM was mediated via interaction with both blastocyst EGFR and heparan sulfate proteoglycan (HSPG). It was concluded that HB-EGF TM, which is synthesized exclusively in the luminal epithelium at the site of blastocyst apposition, and which is a juxtacrine adhesion factor for blastocysts, could be one of the mediators of blastocyst adhesion to the uterus in the process of implantation.

摘要

先前的研究表明,肝素结合表皮生长因子(EGF)样生长因子(HB-EGF)mRNA在小鼠子宫腔上皮中于植入前在时间上合成,且仅在胚泡附着部位在空间上合成(达斯,S.K.,王,X.N.,帕里亚,B.C.,达姆,D.,亚伯拉罕,J.A.,克拉格斯布伦,M.,安德鲁斯,G.K.和戴伊,S.K.(1994年)《发育》120卷,1071 - 1083页)。HB-EGF作为一种跨膜蛋白(HB-EGF TM)合成,该跨膜蛋白可被加工以释放可溶性生长因子。一种仅与跨膜形式发生交叉反应的抗体以与HB-EGF mRNA相似的空间方式在子宫腔上皮中检测到HB-EGF TM。HB-EGF TM是一种介导细胞间接触的旁分泌生长因子。为了确定HB-EGF TM是否可能是胚泡的黏附因子,将合成人HB-EGF TM的小鼠细胞系与小鼠胚泡共培养。合成HB-EGF TM的细胞比亲代细胞或合成组成型分泌形式HB-EGF的细胞更广泛地黏附于第4天的小鼠胚泡。合成HB-EGF TM的细胞与胚泡的黏附被过量的重组HB-EGF抑制,但被转化生长因子-α抑制的程度较小。黏附也被对应于HB-EGF肝素结合域的合成肽P21以及用肝素酶孵育胚泡所抑制。此外,相对于正常胚泡,与缺乏表皮生长因子受体(EGFR)的延迟植入休眠胚泡的黏附减少。这些结果表明,胚泡与合成HB-EGF TM的细胞之间的黏附是通过与胚泡EGFR和硫酸乙酰肝素蛋白聚糖(HSPG)两者的相互作用介导的。得出的结论是,仅在胚泡附着部位的腔上皮中合成且是胚泡旁分泌黏附因子的HB-EGF TM可能是植入过程中胚泡与子宫黏附的介质之一。

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