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膀胱平滑肌发育中的间充质-上皮相互作用:上皮特异性

Mesenchymal-epithelial interactions in bladder smooth muscle development: epithelial specificity.

作者信息

DiSandro M J, Li Y, Baskin L S, Hayward S, Cunha G

机构信息

Department of Urology, University of California, San Francisco 94143, USA.

出版信息

J Urol. 1998 Sep;160(3 Pt 2):1040-6; discussion 1079. doi: 10.1097/00005392-199809020-00022.

Abstract

PURPOSE

We previously showed that mesenchymal-epithelial interactions are necessary for the development of bladder smooth muscle. Specifically without bladder epithelium embryonic bladder mesenchyme does not differentiate into smooth muscle. We determine whether this process is specific to bladder epithelium or whether epithelial cells from other organ systems induce bladder mesenchyme to differentiate into smooth muscle, as well as whether epithelial age is an important variable.

MATERIALS AND METHODS

We recombined 14-day bladder mesenchyme before smooth muscle differentiation with rat epithelium from 14-day, 19-day, newborn and adult bladder, ureter, colon, ileum, stomach, cornea and epidermis. In addition, bladder epithelium was recombined with 14-day embryonic small intestinal, 14-day embryonic gastric and newborn seminal vesicle mesenchyme. All tissue recombinants were grafted under the renal capsule of an adult rat syngeneic host for 3 weeks.

RESULTS

Immunohistochemical analysis with antibodies directed against smooth muscle alpha-actin revealed that all epithelial types studied induced bladder mesenchyme to differentiate into smooth muscle, although to different degrees. Induction of smooth muscle was independent of urothelial age. In addition, bladder epithelium induced intestinal, gastric and seminal vesicle mesenchyme to differentiate into smooth muscle and express an overall morphological pattern indicative of the bladder fibromuscular wall.

CONCLUSIONS

The mechanism whereby urothelium induces bladder mesenchyme to differentiate into smooth muscle is not specific to embryonic urothelium. Older urothelium and heterotypic epithelium also induce smooth muscle differentiation. With the common use of bowel, stomach and ureteral segments for bladder augmentation it is important to understand the interaction of different types of epithelium with the native bladder.

摘要

目的

我们之前的研究表明,间充质 - 上皮相互作用对于膀胱平滑肌的发育是必需的。具体而言,没有膀胱上皮,胚胎膀胱间充质就不会分化为平滑肌。我们要确定这个过程是否仅针对膀胱上皮,还是来自其他器官系统的上皮细胞也能诱导膀胱间充质分化为平滑肌,以及上皮细胞的年龄是否是一个重要变量。

材料与方法

我们将14天龄、平滑肌尚未分化的膀胱间充质与来自14天龄、19天龄、新生及成年大鼠的膀胱、输尿管、结肠、回肠、胃、角膜和表皮的上皮进行重组。此外,还将膀胱上皮与14天龄胚胎小肠、14天龄胚胎胃及新生精囊间充质进行重组。所有组织重组体均移植到同基因成年大鼠宿主的肾被膜下3周。

结果

用抗平滑肌α - 肌动蛋白抗体进行免疫组织化学分析显示,尽管程度不同,但所有研究的上皮类型均能诱导膀胱间充质分化为平滑肌。平滑肌的诱导与尿路上皮的年龄无关。此外,膀胱上皮能诱导小肠、胃和精囊间充质分化为平滑肌,并呈现出指示膀胱纤维肌壁的整体形态模式。

结论

尿路上皮诱导膀胱间充质分化为平滑肌的机制并非胚胎尿路上皮所特有。较老的尿路上皮和异型上皮也能诱导平滑肌分化。鉴于在膀胱扩大术中常用肠段、胃段和输尿管段,了解不同类型上皮与天然膀胱之间的相互作用很重要。

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