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Cellular localization of guanylin and uroguanylin mRNAs in human and rat duodenal and colonic mucosa

机译:人和大鼠十二指肠和结肠黏膜中鸟苷和尿鸟苷mRNA的细胞定位

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摘要

Guanylin (GUCA2A/Guca2a/GN) and uroguanylin (GUCA2B/Guca2b/UGN) are expressed in the gastrointestinal tract and have been implicated in ion and fluid homeostasis, satiety, abdominal pain, growth and intestinal barrier integrity. Their cellular sources are debated and include goblet cells, entero-/colonocytes, enteroendocrine (EE) cells and tuft cells. We therefore investigated the cellular sources of GN and UGN mRNAs in human and rat duodenal and colonic epithelium with in situ hybridization (ISH) to determine co-expression with Chromogranin A (CHGA/Chga/CgA; enterochromaffin [EC] cells), defensin alpha 6 (DEFA6/Defa6; Paneth cells), mucin 2 (MUC2/Muc2; goblet cells) and selected tuft cell markers. GUCA2A/Guca2a expression was localized to goblet cells and colonocytes in human and rat colon. In human duodenum, GUCA2A was expressed in Paneth cells and was scarce in villous epithelial cells. In rat duodenum, Guca2a was only localized to goblet cells. Guca2b was focally expressed in rat colon. In human and rat duodenum and in human colon, GUCA2B/Guca2b was expressed in dispersed solitary epithelial cells, some with a tuft cell-like appearance. Neither GUCA2A nor GUCA2B were co-expressed with CHGA in human duodenal cells. Consequently, EC cells are probably not the major source of human GN or UGN but other EE cells as a source of GN or UGN are not entirely excluded. No convincing overlap with tuft cell markers was found. For the first time, we demonstrate the cellular expression of GUCA2B in human duodenum. The specific cellular distribution of both GN and UGN differs between duodenum and colon and between human and rat intestines.Electronic supplementary materialThe online version of this article (doi:10.1007/s00441-016-2393-y) contains supplementary material, which is available to authorized users.
机译:鸟苷蛋白(GUCA2A / Guca2a / GN)和尿鸟苷蛋白(GUCA2B / Guca2b / UGN)在胃肠道中表达,与离子和体液稳态,饱腹感,腹痛,生长和肠屏障完整性有关。他们的细胞来源受到争议,包括杯状细胞,肠/结肠细胞,肠内分泌(EE)细胞和簇绒细胞。因此,我们通过原位杂交(ISH)研究了人和大鼠十二指肠和结肠上皮中GN和UGN mRNA的细胞来源,以确定与嗜铬粒蛋白A(CHGA / Chga / CgA;肠嗜铬细胞[EC]细胞),防御素α的共表达6(DEFA6 / Defa6; Paneth细胞),粘蛋白2(MUC2 / Muc2;杯状细胞)和选定的簇状细胞标记。 GUCA2A / Guca2a表达局限于人和大鼠结肠中的杯状细胞和结肠细胞。在人十二指肠中,GUCA2A在Paneth细胞中表达,而在绒毛上皮细胞中缺乏。在大鼠十二指肠中,Guca2a仅定位于杯状细胞。 Guca2b在大鼠结肠中局部表达。在人和大鼠十二指肠以及人结肠中,GUCA2B / Guca2b 在分散的孤立上皮细胞中表达,有些具有簇状细胞外观。 GUCA2A GUCA2B 在人十二指肠细胞中均未与 CHGA 共表达。因此,EC细胞可能不是人类GN或UGN的主要来源,但作为GN或UGN的来源的其他EE细胞却没有被完全排除。没有发现与簇细胞标记的令人信服的重叠。我们首次展示了 GUCA2B 在人十二指肠中的细胞表达。十二指肠和结肠之间以及人和大鼠小肠之间GN和UGN的特定细胞分布有所不同电子补充材料本文的在线版本(doi:10.1007 / s00441-016-2393-y)包含补充材料,可用于授权用户。

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