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Microvessels support engraftment and functionality of human islets and hESC-derived pancreatic progenitors in diabetes models
Cell Stem Cell ( IF 23.9 ) Pub Date : 2021-09-03 , DOI: 10.1016/j.stem.2021.08.001
Yasaman Aghazadeh 1 , Frankie Poon 2 , Farida Sarangi 3 , Frances T M Wong 4 , Safwat T Khan 5 , Xuetao Sun 6 , Rupal Hatkar 6 , Brian J Cox 7 , Sara S Nunes 8 , M Cristina Nostro 2
Affiliation  

Islet transplantation is a promising treatment for type 1 diabetes (T1D), yet the low donor pool, poor islet engraftment, and life-long immunosuppression prevent it from becoming the standard of care. Human embryonic stem cell (hESC)-derived pancreatic cells could eliminate donor shortages, but interventions to improve graft survival are needed. Here, we enhanced subcutaneous engraftment by employing a unique vascularization strategy based on ready-made microvessels (MVs) isolated from the adipose tissue. This resulted in improved cell survival and effective glucose response of both human islets and hESC-derived pancreatic cells, which ameliorated preexisting diabetes in three mouse models of T1D.



中文翻译:

微血管支持糖尿病模型中人类胰岛和 hESC 衍生的胰腺祖细胞的植入和功能

胰岛移植是治疗 1 型糖尿病 (T1D) 的一种有前途的治疗方法,但供体库低、胰岛移植不良和终生免疫抑制使其无法成为治疗标准。人类胚胎干细胞 (hESC) 衍生的胰腺细胞可以消除供体短缺,但需要采取干预措施来提高移植物的存活率。在这里,我们通过采用基于从脂肪组织中分离出来的现成微血管 (MV) 的独特血管化策略来增强皮下植入。这导致人类胰岛和 hESC 衍生胰腺细胞的细胞存活率和有效葡萄糖反应得到改善,从而改善了三种 T1D 小鼠模型中先前存在的糖尿病。

更新日期:2021-11-04
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