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激素在小鼠乳腺器官培养中诱导视黄酸结合蛋白的作用。

Role of hormones on the induction of retinoic acid binding protein in mouse mammary gland organ culture.

作者信息

Mehta R G, Moon R C

出版信息

Carcinogenesis. 1985 Aug;6(8):1103-7. doi: 10.1093/carcin/6.8.1103.

Abstract

Influence of various hormones on the induction of cellular retinoic acid binding protein (CRABP) was investigated in the mouse mammary gland organ cultures. Thoracic pairs of mammary glands from the BALB/c mice were cultured for seven days in the presence of various hormones in CMRL medium at 37 degrees C under 50% O2, 5% CO2 and 45% N2 atmosphere. There was a modest increase of mammary CRABP by insulin (I) + prolactin (P), however, addition of progesterone (Pg) or estrogen (E) + Pg to the medium resulted in a dramatic increase in the CRABP. Aldosterone (A) + hydrocortisone (F), in addition to I + P, which promotes differentiation to an extent similar to that of I + P + E + Pg did not have any influence on the induction of CRABP. These results indicate that prolactin and/or Pg in the medium can increase the concentration of CRABP in the mammary gland in vitro. From the results presented in this report, as well as previous work by other investigators, it is concluded that the biological response to retinoids in the mammary tissues cannot be correlated with the absolute concentration of CRABP in the cells. However, the biological response may be dependent upon both the ability of the target organ cells to metabolize the retinoid and to have minimal concentration of CRABP for binding to the active metabolite. The functional significance of hormone-induced CRABP is presently unknown.

摘要

在小鼠乳腺器官培养物中研究了各种激素对细胞视黄酸结合蛋白(CRABP)诱导的影响。将来自BALB/c小鼠的胸部乳腺对在含有各种激素的CMRL培养基中于37℃、50% O2、5% CO2和45% N2气氛下培养7天。胰岛素(I)+催乳素(P)使乳腺CRABP有适度增加,然而,向培养基中添加孕酮(Pg)或雌激素(E)+Pg会导致CRABP急剧增加。醛固酮(A)+氢化可的松(F),除了I + P外,在促进分化方面与I + P + E + Pg程度相似,但对CRABP的诱导没有任何影响。这些结果表明,培养基中的催乳素和/或Pg可在体外增加乳腺中CRABP的浓度。根据本报告中的结果以及其他研究者先前的工作,可以得出结论,乳腺组织中对视黄酸的生物学反应与细胞中CRABP的绝对浓度无关。然而,生物学反应可能既取决于靶器官细胞代谢视黄酸的能力,也取决于具有与活性代谢物结合的最低浓度的CRABP。激素诱导的CRABP的功能意义目前尚不清楚。

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