Division of General and Thoracic Surgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
Translational Medicine Program, The Hospital for Sick Children, Toronto, Ontario, Canada.
PLoS One. 2021 Dec 2;16(12):e0260522. doi: 10.1371/journal.pone.0260522. eCollection 2021.
Necrotizing enterocolitis (NEC) is one of the most distressing gastrointestinal emergencies affecting neonates. Amniotic fluid stem cells (AFSC) improve intestinal injury and survival in experimental NEC but are difficult to administer. In this study, we evaluated whether conditioned medium (CM) derived from human AFSC have protective effects.
Three groups of C57BL/6 mice were studied: (i) breast-fed mice as control; (ii) experimental NEC mice receiving PBS; and (iii) experimental NEC mice receiving CM. NEC was induced between post-natal days P5 through P9 via: (A) gavage feeding of hyperosmolar formula four-time a day; (B) 10 minutes hypoxia prior to feeds; and (C) lipopolysaccharide administration on P6 and P7. Intra-peritoneal injections of either PBS or CM were given on P6 and P7. All mice were sacrificed on P9 and terminal ileum were harvested for analyses.
CM treatment increased survival and reduced intestinal damage, decreased mucosal inflammation (IL-6; TNF-α), neutrophil infiltration (MPO), and apoptosis (CC3), and also restored angiogenesis (VEGF) in the ileum. Additionally, CM treated mice had increased levels of epithelial proliferation (Ki67) and stem cell activity (Olfm4; Lgr5) compared to NEC+PBS mice, showing restored intestinal regeneration and recovery during NEC induction. CM proteomic analysis of CM content identified peptides that regulated immune and stem cell activity.
CM derived from human AFSC administered in experimental NEC exhibited various benefits including reduced intestinal injury and inflammation, increased enterocyte proliferation, and restored intestinal stem cell activity. This study provides the scientific basis for the use of CM derived from AFSC in neonates with NEC.
坏死性小肠结肠炎(NEC)是影响新生儿的最令人痛苦的胃肠道急症之一。羊水干细胞(AFSC)可改善实验性 NEC 中的肠道损伤和存活率,但难以给药。在这项研究中,我们评估了源自人 AFSC 的条件培养基(CM)是否具有保护作用。
研究了三组 C57BL/6 小鼠:(i)母乳喂养的小鼠作为对照;(ii)接受 PBS 的实验性 NEC 小鼠;(iii)接受 CM 的实验性 NEC 小鼠。通过以下方式在出生后第 5 天至第 9 天之间诱导 NEC:(A)每天四次通过胃管给予高渗配方;(B)在喂养前 10 分钟缺氧;(C)在第 6 天和第 7 天给予脂多糖。在第 6 天和第 7 天分别给予 PBS 或 CM 的腹腔内注射。所有小鼠均于第 9 天处死,并采集末端回肠进行分析。
CM 治疗增加了存活率并减轻了肠道损伤,减少了粘膜炎症(IL-6;TNF-α)、中性粒细胞浸润(MPO)和细胞凋亡(CC3),并恢复了回肠中的血管生成(VEGF)。此外,与 NEC+PBS 小鼠相比,CM 治疗的小鼠上皮细胞增殖(Ki67)和干细胞活性(Olfm4;Lgr5)增加,表明在 NEC 诱导期间肠道再生和恢复。CM 对 CM 内容物的蛋白质组分析鉴定出调节免疫和干细胞活性的肽。
在实验性 NEC 中给予源自人 AFSC 的 CM 表现出多种益处,包括减轻肠道损伤和炎症、增加肠细胞增殖和恢复肠道干细胞活性。这项研究为在患有 NEC 的新生儿中使用源自 AFSC 的 CM 提供了科学依据。