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前列腺类固醇结合蛋白(PSBP)基因的转录由上皮-间质相互作用诱导。

Transcription of prostatic steroid binding protein (PSBP) gene is induced by epithelial-mesenchymal interaction.

作者信息

Takeda H, Suematsu N, Mizuno T

机构信息

Zoological Institute, Faculty of Science, University of Tokyo, Japan.

出版信息

Development. 1990 Sep;110(1):273-81. doi: 10.1242/dev.110.1.273.

Abstract

The prostate gland develops from the fetal urogenital sinus at the base of the urinary bladder. It finally differentiates into three lobes; ventral, lateral and dorsal lobes of the prostate. In spite of their common developmental origin and similar glandular structure, these lobes show the different biochemical characteristics, for example, in the proteins they secrete. In the present study, we investigate the involvement of the epithelial-mesenchymal interaction in the lobe-specific differentiation of the prostatic epithelium by means of epithelial-mesenchymal recombination experiments. We have used a prostatic steroid-binding protein (PSBP) as a specific differentiation marker for the ventral prostate. PSBP is a tetramer which consists of 2 sub-units, one containing the polypeptides C1 and C3 and the other containing the polypeptides C2 and C3. Northern analysis with a complementary DNA probe encoding C1 peptide (PSBP-C1) revealed that the mRNAs were detected exclusively in the ventral prostate but not in the dorsal prostate or in other organs such as urinary bladder and kidney. In situ hybridization with a complementary (anti-sense) RNA probe demonstrated that the transcripts were found only in the epithelium, not in the mesenchyme of the ventral prostate. In situ hybridization also showed that, in normal development, the mRNAs for PSBP-C1 in the ventral epithelium were first detectable at day 14 after birth, coinciding with the onset of its cytodifferentiation, and that they reached mature levels by day 21. We then carried out tissue-recombination experiments to examine whether the transcription of the PSBP-C1 gene in the epithelium is affected by the surrounding mesenchyme. Fetal urogenital sinuses were subdivided into ventral and dorsal halves. Following collagenase treatment, both halves were separated into their epithelial and mesenchymal compartments. Homotypic (ventral epithelium plus ventral mesenchyme [Ev/Mv] and dorsal epithelium plus dorsal mesenchyme [Ed/Md]) and heterotypic (ventral epithelium plus dorsal mesenchyme [Ev/Md] and dorsal epithelium plus ventral mesenchyme [Ed/Mv]) recombinations were carried out. After 4-5 weeks of growth in male host, the glandular structures characteristic for prostate glands were formed in all explants. However, in situ hybridization revealed the transcripts of the PSBP-C1 gene only in the epithelium associated with the ventral mesenchyme (Ev/Mv and Ed/Mv).(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

前列腺由膀胱底部的胎儿泌尿生殖窦发育而来。它最终分化为三个叶,即前列腺的腹侧叶、外侧叶和背侧叶。尽管这些叶有着共同的发育起源和相似的腺结构,但它们表现出不同的生化特性,例如,它们所分泌的蛋白质不同。在本研究中,我们通过上皮 - 间充质重组实验,研究上皮 - 间充质相互作用在前列腺上皮叶特异性分化中的作用。我们使用前列腺类固醇结合蛋白(PSBP)作为腹侧前列腺的特异性分化标志物。PSBP是一种四聚体,由两个亚基组成,一个包含多肽C1和C3,另一个包含多肽C2和C3。用编码C1肽(PSBP - C1)的互补DNA探针进行Northern分析表明,mRNA仅在腹侧前列腺中检测到,而在背侧前列腺或膀胱和肾脏等其他器官中未检测到。用互补(反义)RNA探针进行原位杂交表明,转录本仅在上皮细胞中发现,而不在腹侧前列腺的间充质中。原位杂交还表明,在正常发育过程中,腹侧上皮中PSBP - C1的mRNA在出生后第14天首次可检测到,这与其细胞分化的开始相吻合,并且在第21天达到成熟水平。然后我们进行了组织重组实验,以检查上皮中PSBP - C1基因的转录是否受周围间充质的影响。胎儿泌尿生殖窦被分为腹侧和背侧两半。经胶原酶处理后,两半分别分离为上皮和间充质部分。进行了同型(腹侧上皮加腹侧间充质[Ev/Mv]和背侧上皮加背侧间充质[Ed/Md])和异型(腹侧上皮加背侧间充质[Ev/Md]和背侧上皮加腹侧间充质[Ed/Mv])重组。在雄性宿主中生长4 - 5周后,所有外植体中都形成了前列腺特有的腺结构。然而,原位杂交显示PSBP - C1基因的转录本仅在与腹侧间充质相关的上皮中(Ev/Mv和Ed/Mv)。(摘要截于400字)

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