以弹性蛋白为基础的血管生成支架可促进边缘胰岛块在肝外部位的植入和功能

Silvia Minardi , Michelle Guo , Xiaomin Zhang , Xunrong Luo
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引用次数: 7

摘要

在胰岛移植中,最佳移植的主要障碍之一是在胰岛分离过程中胰岛自然血管化和胰岛特异性细胞外基质(ECM)的丧失。因此,移植的胰岛必须通过形成新血管和新的ECM来重建营养和物理支持。为了促进这一关键过程,我们开发了一种基于弹性蛋白的血管生成和ecm促进支架,用于肝外胰岛移植。设计的支架由I型胶原(Coll)与20wt%的弹性蛋白(E)混合组成,可以促进血管生成和新生ECM沉积。由此产生的“CollE”支架具有相互连接的孔,其大小分布适合于胰岛的播种和新血管的生长。体外,CollE支架能够延长小鼠胰岛的培养时间长达一周,同时保持其完整性、活力和功能。在体内,在边缘胰岛块移植后仅四周,CollE支架显示附睾脂肪垫移植胰岛的血管化增强,并促进先前糖尿病受体的高血糖迅速逆转。该结果与肾包膜(KC)胰岛移植相当,优于在对照胶原支架(Coll)上移植的胰岛。与Coll支架相比,与血管生成相关的关键基因(VEGFA、PDGFB、FGF1和COL3A1)以及新生胰岛特异性基质沉积(COL6A1、COL4A1、LAMA2和FN1)在CollE支架上的胰岛中均显著上调。最后,CollE支架也能够支持人类胰岛的体外培养。综上所述,CollE支架通过促进血管生成和胰岛特异性ECM沉积,有可能改善肝外边缘胰岛移植的临床结果。
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An elastin-based vasculogenic scaffold promotes marginal islet mass engraftment and function at an extrahepatic site

In islet transplantation, one of the major obstacles to optimal engraftment is the loss of islet natural vascularization and islet-specific extracellular matrix (ECM) during the islet isolation process. Thus, transplanted islets must re-establish nutritional and physical support through formation of new blood vessels and new ECM. To promote this critical process, we developed an elastin-based vasculogenic and ECM-promoting scaffold engineered for extrahepatic islet transplantation. The scaffold by design consisted of type I collagen (Coll) blended with 20wt% of elastin (E) shown to promote angiogenesis as well as de novo ECM deposition. The resulting “CollE” scaffolds had interconnected pores with a size distribution tailored to accommodate seeding of islets as well as growth of new blood vessels. In vitro, CollE scaffolds enabled prolonged culture of murine islets for up to one week while preserving their integrity, viability and function. In vivo, after only four weeks post-transplant of a marginal islet mass, CollE scaffolds demonstrated enhanced vascularization of the transplanted islets in the epididymal fat pad and promoted a prompt reversal of hyperglycemia in previously diabetic recipients. This outcome was comparable to that of kidney capsular (KC) islet transplantation, and superior to that of islets transplanted on the control collagen-only scaffolds (Coll). Crucial genes associated with angiogenesis (VEGFA, PDGFB, FGF1, and COL3A1) as well as de novo islet-specific matrix deposition (COL6A1, COL4A1, LAMA2 and FN1) were all significantly upregulated in islets on CollE scaffolds in comparison to those on Coll scaffolds. Finally, CollE scaffolds were also able to support human islet culture in vitro. In conclusion, CollE scaffolds have the potential to improve the clinical outcome of marginal islet transplantation at extrahepatic sites by promoting angiogenesis and islet-specific ECM deposition.

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