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蜕膜细胞功能:仓鼠妊娠早期血清皮质类固醇结合球蛋白及一种60 kDa蛋白调节作用的证据。

Decidual cell function: evidence for a role in the regulation of serum CBG and a 60 kDa protein during early pregnancy in the hamster.

作者信息

Leavitt W W, Rundle S, Thompson K, Selcer K W, Gray G O

机构信息

Department of Biochemistry, Texas Tech University Health Sciences Center, Lubbock.

出版信息

Adv Exp Med Biol. 1987;230:187-205. doi: 10.1007/978-1-4684-1297-0_11.

Abstract

Several serum proteins increase in titer during pregnancy. We tested the hypothesis that decidual cells may signal the production of certain serum proteins in the hamster. Measurement of serum CBG by equilibrium binding using either [3H]-progesterone or [3H]-cortisol in conjection with ion exchange chromatography showed that decidualization increased CBG levels. Two-dimensional gel electrophoresis revealed that a 60 kDa++ protein increases markedly in the serum of the hormonally pseudopregnant (PSP) animal soon after artificial induction of decidualization on PSP day 4. The 60 kDa serum protein remains low in the nondecidualized PSP animal, but it increases in the pregnant animal. A photoaffinity labeling procedure was used to covalently bind [3H]-androstadienolone to CBG. Fluorography of 2D gels run under denaturing conditions established that the 60 kDa protein did not bind steroid as did CBG (69 kDa). To determine whether decidual cells could induce the 60 kDa and CBG proteins, different numbers of decidual cells were injected IP into PSP recipients. A single injection of 50 x 10(6) decidual cells induced both serum proteins within 48h, whereas the same number of hamster fetal cells was ineffective. Thus, these results demonstrate that hamster decidual cells induce a 60 kDa protein of unknown function and serum CBG. Since the decidual cell itself does not appear to be the source of either protein, it follows that the decidual cell signals the synthesis and secretion of these proteins elsewhere in the body, most likely in the liver. To our knowledge, this is the first demonstration that the decidual cell regulates serum CBG and other proteins in this manner.

摘要

几种血清蛋白在孕期滴度会升高。我们检验了一个假设,即仓鼠的蜕膜细胞可能会发出信号促使某些血清蛋白的产生。通过使用[3H]-孕酮或[3H]-皮质醇结合离子交换色谱法进行平衡结合来测量血清皮质类固醇结合球蛋白(CBG),结果显示蜕膜化会增加CBG水平。二维凝胶电泳显示,在激素诱导假孕(PSP)第4天人工诱导蜕膜化后不久,一种60 kDa++的蛋白质在激素诱导假孕(PSP)动物的血清中显著增加。在未发生蜕膜化的PSP动物中,这种60 kDa的血清蛋白含量较低,但在怀孕动物中会增加。采用光亲和标记法将[3H]-雄甾二烯酮共价结合到CBG上。在变性条件下运行的二维凝胶的荧光自显影片显示,60 kDa的蛋白质不像CBG(69 kDa)那样能结合类固醇。为了确定蜕膜细胞是否能诱导60 kDa蛋白和CBG蛋白的产生,将不同数量的蜕膜细胞经腹腔注射到PSP受体动物体内。单次注射50×10(6)个蜕膜细胞可在48小时内诱导两种血清蛋白的产生,而相同数量的仓鼠胎儿细胞则无效。因此,这些结果表明仓鼠蜕膜细胞可诱导一种功能未知的60 kDa蛋白和血清CBG。由于蜕膜细胞本身似乎不是这两种蛋白的来源,因此可以推断蜕膜细胞会向身体其他部位(很可能是肝脏)发出信号,促使这些蛋白的合成和分泌。据我们所知,这是首次证明蜕膜细胞以这种方式调节血清CBG和其他蛋白质。

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