Suppr超能文献

白细胞介素6在体外抑制小鼠胎盘催乳素II的分泌,但不抑制小鼠胎盘催乳素I的分泌。

Interleukin 6 inhibits mouse placental lactogen II but not mouse placental lactogen I secretion in vitro.

作者信息

Yamaguchi M, Ogren L, Southard J N, Kurachi H, Miyake A, Talamantes F

机构信息

Department of Biology, University of California, Santa Cruz 95064.

出版信息

Proc Natl Acad Sci U S A. 1993 Dec 15;90(24):11905-9. doi: 10.1073/pnas.90.24.11905.

Abstract

The mouse placenta produces several polypeptides belonging to the prolactin-growth hormone gene family, including mouse placental lactogen (mPL) I and mPL-II. The present study was undertaken to determine whether the secretion of mPL-I and mPL-II is regulated by interleukin 6 (IL-6), which is present in the placenta and has previously been reported to stimulate the secretion of pituitary members of this gene family. Effects of human and mouse IL-6 on mPL-I and mPL-II secretion were examined in primary cultures of placental cells from days 7, 9, and 12 of pregnancy. IL-6 caused a dose-dependent reduction in the mPL-II concentration in the medium of cells from days 9 and 12 of pregnancy but did not affect the mPL-II concentration in the medium of cells from day 7 of pregnancy or the mPL-I concentration in the medium of cells from days 7 or 9 of pregnancy. The lowest concentration of human IL-6 that significantly inhibited mPL-II secretion was 250 pM. The effect of IL-6 on the mPL-II concentration in the medium was due primarily to inhibition of mPL-II synthesis, which resulted at least partly from a decrease in the steady-state level of mPL-II mRNA. These data raise the possibility that IL-6 may regulate mPL-II production after midpregnancy in vivo.

摘要

小鼠胎盘会产生几种属于催乳素 - 生长激素基因家族的多肽,包括小鼠胎盘催乳素(mPL)I和mPL - II。本研究旨在确定mPL - I和mPL - II的分泌是否受白细胞介素6(IL - 6)的调节,IL - 6存在于胎盘中,且此前有报道称其可刺激该基因家族垂体成员的分泌。在妊娠第7、9和12天胎盘细胞的原代培养物中检测了人和小鼠IL - 6对mPL - I和mPL - II分泌的影响。IL - 6导致妊娠第9天和12天细胞培养基中mPL - II浓度呈剂量依赖性降低,但不影响妊娠第7天细胞培养基中mPL - II的浓度,也不影响妊娠第7天或第9天细胞培养基中mPL - I的浓度。显著抑制mPL - II分泌的人IL - 6最低浓度为250 pM。IL - 6对培养基中mPL - II浓度的影响主要是由于抑制了mPL - II的合成,这至少部分是由于mPL - II mRNA稳态水平的降低所致。这些数据增加了IL - 6可能在体内妊娠中期后调节mPL - II产生的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dfd/48093/de6f41d66712/pnas01531-0479-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验