Vasoactive intestinal peptide promotes secretory differentiation and mitigates radiation-induced intestinal injury.

IF 7.1 2区 医学 Q1 CELL & TISSUE ENGINEERING
Tatiana Agibalova, Anneke Hempel, H Carlo Maurer, Mohab Ragab, Anastasia Ermolova, Jessica Wieland, Caroline Waldherr Ávila de Melo, Fabian Heindl, Maximilian Giller, Julius Clemens Fischer, Markus Tschurtschenthaler, Birgit Kohnke-Ertel, Rupert Öllinger, Katja Steiger, Ihsan Ekin Demir, Dieter Saur, Michael Quante, Roland M Schmid, Moritz Middelhoff
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引用次数: 0

Abstract

Background: Vasoactive intestinal peptide (VIP) is a neuronal peptide with prominent distribution along the enteric nervous system. While effects of VIP on intestinal motility, mucosal vasodilation, secretion, and mucosal immune cell function are well-studied, the direct impact of VIP on intestinal epithelial cell turnover and differentiation remains less understood. Intestinal stem and progenitor cells are essential for the maintenance of intestinal homeostasis and regeneration, and their functions can be modulated by factors of the stem cell niche, including neuronal mediators. Here, we investigated the role of VIP in regulating intestinal epithelial homeostasis and regeneration following irradiation-induced injury.

Methods: Jejunal organoids were derived from male and female C57Bl6/J, Lgr5-EGFP-IRES-CreERT2 or Lgr5-EGFP-IRES-CreERT2/R26R-LSL-TdTomato mice and treated with VIP prior to analysis. Injury conditions were induced by exposing organoids to 6 Gy of irradiation (IR). To investigate protective effects of VIP in vivo, mice received 12 Gy of abdominal IR followed by intraperitoneal injections of VIP.

Results: We observed that VIP promotes epithelial differentiation towards a secretory phenotype predominantly via the p38 MAPK pathway. Moreover, VIP prominently modulated epithelial proliferation as well as the number and proliferative activity of Lgr5-EGFP+ progenitor cells under homeostatic conditions. In the context of acute irradiation injury in vitro, we observed that IR injury renders Lgr5-EGFP+ progenitor cells more susceptible to VIP-induced modulations, which coincided with the strong promotion of epithelial regeneration by VIP. Finally, the observed effects translate into an in vivo model of abdominal irradiation, where VIP showed to prominently mitigate radiation-induced injury.

Conclusions: VIP prominently governs intestinal homeostasis by regulating epithelial progenitor cell proliferation and differentiation and promotes intestinal regeneration following acute irradiation injury.

血管活性肠肽促进分泌分化,减轻辐射引起的肠道损伤。
背景:血管活性肠肽(VIP)是一种神经肽,主要分布于肠道神经系统。VIP对肠道蠕动、粘膜血管扩张、分泌和粘膜免疫细胞功能的影响已得到充分研究,但VIP对肠上皮细胞更替和分化的直接影响仍鲜为人知。肠道干细胞和祖细胞对维持肠道平衡和再生至关重要,其功能可受干细胞龛因子(包括神经元介质)的调节。在此,我们研究了VIP在辐照损伤后调节肠上皮稳态和再生中的作用:方法:从雌雄 C57Bl6/J、Lgr5-EGFP-IRES-CreERT2 或 Lgr5-EGFP-IRES-CreERT2/R26R-LSL-TdTomato 小鼠中提取空肠器官组织,分析前用 VIP 处理。将器官组织暴露于 6 Gy 的辐照 (IR) 中诱发损伤。为了研究 VIP 在体内的保护作用,小鼠腹部接受了 12 Gy 的红外线照射,然后腹腔注射 VIP:结果:我们观察到,VIP 主要通过 p38 MAPK 通路促进上皮细胞向分泌表型分化。此外,VIP 还能显著调节上皮细胞的增殖,以及平衡状态下 Lgr5-EGFP+ 祖细胞的数量和增殖活性。在体外急性辐照损伤的情况下,我们观察到红外损伤使 Lgr5-EGFP+ 祖细胞更易受 VIP 诱导的调节作用的影响,这与 VIP 强力促进上皮再生的作用不谋而合。最后,观察到的效应转化到腹部照射的体内模型中,VIP 显示出显著减轻辐射诱导的损伤:结论:VIP 通过调节上皮祖细胞的增殖和分化,显著调节肠道稳态,并促进急性辐照损伤后的肠道再生。
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来源期刊
Stem Cell Research & Therapy
Stem Cell Research & Therapy CELL BIOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
CiteScore
13.20
自引率
8.00%
发文量
525
审稿时长
1 months
期刊介绍: Stem Cell Research & Therapy serves as a leading platform for translational research in stem cell therapies. This international, peer-reviewed journal publishes high-quality open-access research articles, with a focus on basic, translational, and clinical research in stem cell therapeutics and regenerative therapies. Coverage includes animal models and clinical trials. Additionally, the journal offers reviews, viewpoints, commentaries, and reports.
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