用于脂肪来源的间充质干细胞向胰岛样干细胞簇分化的三维湿式电纺丝支架系统

IF 3.1 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jijo Wilson, V. G. Rahul, Lynda V. Thomas, Prabha D. Nair
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引用次数: 3

摘要

干细胞衍生的胰岛样细胞簇(ILCs)是治疗糖尿病的胰腺β细胞的另一种来源。由于胰岛细胞在2D培养系统中聚集,理想的3D培养平台对于产生所需簇大小的ILCs是一个挑战。在二维条件下培养的胰岛细胞产生大尺寸的簇,在胰岛素分泌和活力方面效率较低。在这项研究中,我们报告了与在传统电纺丝片上培养相比,在具有较大孔径的pcl基湿式电纺丝纤维支架上形成的ILCs产生所需尺寸的簇。胶原功能化后的湿式电纺聚己内酯(PCL)支架与非功能化或常规电纺聚己内酯支架相比,胰岛素分泌和细胞活力增强。胶原涂层湿式电纺丝3D支架产生的ILC簇直径为70±20 μm,而常规电纺丝PCL片产生的ILC簇直径为300±10 μm。因此,胶原功能化湿式电纺丝支架系统可能是一种潜在的胰岛组织工程支架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three-dimensional wet electrospun scaffold system for the differentiation of adipose-derived mesenchymal stem cells to islet-like clusters

Stem cell-derived islet-like clusters (ILCs) are an alternative source of pancreatic beta cells for the treatment of diabetic mellitus. An ideal 3D culture platform for the generation of ILCs of desired cluster size is a challenge due to the clustering of islet cells in the 2D culture systems. The islet cells cultured in 2D conditions produce clusters of large size, which are less efficient in terms of insulin secretion and viability. In this study, we report that ILCs formed on a PCL-based wet electrospun fibrous scaffold with larger pore size produced clusters of the desired size, compared to that cultured on a conventional electrospun sheet. The collagen functionalization on this wet electrospun polycaprolactone (PCL) scaffold showed enhanced insulin secretion and cell viability compared to the non-functionalized or conventionally electrospun PCL scaffold. The collagen-coated wet electrospun 3D scaffold produced ILCs of cluster diameter 70 ± 20 μm and the conventionally electrospun PCL sheet produced larger ILC clusters of diameter 300 ± 10 μm. Hence the results indicate the collagen-functionalized wet electrospun scaffold system could be a potential scaffold for islet tissue engineering.

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来源期刊
CiteScore
7.50
自引率
3.00%
发文量
97
审稿时长
4-8 weeks
期刊介绍: Journal of Tissue Engineering and Regenerative Medicine publishes rapidly and rigorously peer-reviewed research papers, reviews, clinical case reports, perspectives, and short communications on topics relevant to the development of therapeutic approaches which combine stem or progenitor cells, biomaterials and scaffolds, growth factors and other bioactive agents, and their respective constructs. All papers should deal with research that has a direct or potential impact on the development of novel clinical approaches for the regeneration or repair of tissues and organs. The journal is multidisciplinary, covering the combination of the principles of life sciences and engineering in efforts to advance medicine and clinical strategies. The journal focuses on the use of cells, materials, and biochemical/mechanical factors in the development of biological functional substitutes that restore, maintain, or improve tissue or organ function. The journal publishes research on any tissue or organ and covers all key aspects of the field, including the development of new biomaterials and processing of scaffolds; the use of different types of cells (mainly stem and progenitor cells) and their culture in specific bioreactors; studies in relevant animal models; and clinical trials in human patients performed under strict regulatory and ethical frameworks. Manuscripts describing the use of advanced methods for the characterization of engineered tissues are also of special interest to the journal readership.
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