Colon-targeted EMSCs conditional medium hydrogel for treatment of ulcerative colitis in mice

溃疡性结肠炎 芍药苷 体内 免疫印迹 结肠炎 医学 化学 病理 胃肠病学 生物 色谱法 生物化学 生物技术 基因 高效液相色谱法 疾病
作者
Wenjing Yang,Xingxing Zhang,Liuyao Qi,Zhe Wang,Weijiang Wu,Wenjing Feng,Yahan Gu
出处
期刊:Biomedical Materials [IOP Publishing]
卷期号:18 (6): 065010-065010 被引量:4
标识
DOI:10.1088/1748-605x/acfadb
摘要

Oral ecto-mesenchymal stem cells-conditional medium (EMSCs-CM) is a promising strategy for treating ulcerative colitis (UC). However, this therapy is currently limited by the harsh gastrointestinal environment and poor colonic targeting ability. Herein, a glutamine transaminase 2 (TG2) crosslinked EMSCs-CM hydrogel (EMSCs-CM-Gel) was fabricated by combining EMSCs-CM with negatively chargedγ-polyglutamic acid (γ-PGA) hydrogel. Intestinal epithelial cell 6 (IEC-6) was applied to construct a cell model with lipopolysaccharide to evaluate the anti-inflammatory potential of EMSCs-CMin vitro. The crosslinked gel was orally administered to mice in liquid form to access the effects of EMSCs-CM-Gelin vivo. This study was based on the fact that the hydrogel containing EMSCs-CM has negative charges, which ensure it remains at the positively charged inflamed colon tissue. The EMSCs-CM could continuously be released in the damaged colon mucosa along with the degradation of theγ-PGA hydrogel. Immunofluorescence and western blot were performed to assess the effects of EMSCs-CM-Gel on mice. The resultsin vivoshowed that EMSCs-CM-Gel could significantly suppress the expression of inflammatory cytokines, prevent the shortening of the length of the intestine and repair the intestinal barrier. Collectively, our findings provided a novel colon-targeted strategy, hoping to benefit UC patients a lot.
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