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大鼠腹侧前列腺上皮细胞和非上皮细胞的活细胞分离

Isolation of viable rat ventral prostate epithelial and nonepithelial cells.

作者信息

Rubenstein M, Anderson K M

出版信息

Endocrinology. 1980 Feb;106(2):530-40. doi: 10.1210/endo-106-2-530.

Abstract

A procedure is described for the dispersion, partial purification, and identification of epithelial and nonepithelial cells from the rat ventral prostate, the latter based in part upon the ability of cells to bind androgen. Since initial efforts to mechanically disrupt prostatic tissue at 2 C lysed many cells, minced rat prostates were exposed to collagenase at 37 C and further dispersed by repetitive pipetting and passage through a tissue sieve. Washed cells in culture medium were centrifuged through an isokinetic Ficoll gradient from which three visible fraction (1, 2, and 4) and a less definite fraction 3 were harvested. Characterically, fraction 1 contained cellular debris; fraction 2 contained round nucleated cells, fewer elliptically shaped cells, red blood cells, and rare free cell nuclei; fraction 3 contained somewhat larger elliptical and round cells; and fraction 4 contained larger round and elliptically shaped cells. These were epithelial cells, as judged by electron microscopy. Isolated prostate cells from rats castrated for 24 h were incubated with [3H]testosterone; 80-90% of the retained radioactivity, the majority of which was dihydrotestosterone, was associated with washed cells from fraction 4. Similar results were obtained after in vivo administration of labeled androgen and subsequent analysis of radioactivity in cells from these fractions. Histochemically and enzymatically demonstrable formalin-insensitive acid phosphatase was increased in bands 3 and 4, which were enriched in epithelial cells. Many cells in fractions 2-4 were viable before and after exposure to Ficoll, as estimated by their ability to exclude trypan blue, incorporate radioactive uridine into RNA, generate cell monolayers during 1-4 weeks of culture, and actively metabolize androgens. Compared to fraction 4, cells from fraction 2, considered to be enriched in nonepithelial cells, actively metabolized but bound much less [3H]testosterone and its metabolites. A number of epithelial cells in fraction 4 isolated from prostates dissociated at 2 C were associated with typical-C-type RNA viruses.

摘要

本文描述了一种从大鼠腹侧前列腺中分离、部分纯化和鉴定上皮细胞和非上皮细胞的方法,后者部分基于细胞结合雄激素的能力。由于最初在2℃下机械破坏前列腺组织的尝试导致许多细胞裂解,因此将切碎的大鼠前列腺在37℃下暴露于胶原酶,并通过反复吹打和通过组织筛进一步分散。将培养基中洗涤过的细胞通过等速菲可梯度离心,从中收获三个可见部分(1、2和4)以及一个不太明确的部分3。典型地,部分1含有细胞碎片;部分2含有圆形有核细胞、较少的椭圆形细胞、红细胞和罕见的游离细胞核;部分3含有稍大的椭圆形和圆形细胞;部分4含有较大的圆形和椭圆形细胞。通过电子显微镜判断,这些是上皮细胞。将阉割24小时的大鼠分离出的前列腺细胞与[3H]睾酮一起孵育;保留放射性的80-90%,其中大部分是双氢睾酮,与部分4的洗涤细胞相关。在体内给予标记雄激素并随后分析这些部分细胞中的放射性后,也获得了类似的结果。在富含上皮细胞的部分3和4中,组织化学和酶学可证实的对福尔马林不敏感的酸性磷酸酶增加。通过其排除台盼蓝、将放射性尿苷掺入RNA、在培养1-4周期间形成细胞单层以及积极代谢雄激素的能力估计,部分2-4中的许多细胞在暴露于菲可之前和之后都是活的。与部分4相比,被认为富含非上皮细胞的部分2中的细胞积极代谢但结合的[3H]睾酮及其代谢物要少得多。从2℃解离的前列腺中分离出的部分4中的许多上皮细胞与典型的C型RNA病毒相关。

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