In Vitro Biological Performance of Alginate Hydrogel Capsules for Stem Cell Delivery

被引:15
作者
de Souza, Jaqueline Brandao [1 ]
Rosa, Gustavo dos Santos [1 ]
Rossi, Mariana Correa [1 ]
Stievani, Fernanda de Castro [1 ]
Pfeifer, Joao Pedro Hubbe [1 ]
Teramoto Krieck, Andre Massahiro [1 ]
de Carvalho Bovolato, Ana Livia [2 ]
Fonseca-Alves, Carlos Eduardo [1 ,3 ]
Amigo Borras, Vicente [4 ]
Garcia Alves, Ana Liz [1 ]
机构
[1] Sao Paulo State Univ, Sch Vet Med & Anim Sci, Dept Vet Surg & Anim Reprod, UNESP, Botucatu, SP, Brazil
[2] Sao Paulo State Univ, Blood Transfus Ctr, UNESP, Cell Engn Lab,Botucatu Med Sch, Botucatu, SP, Brazil
[3] Paulista Univ UNIP Bauru, Inst Hlth Sci, Bauru, SP, Brazil
[4] Univ Politecn Valencia, Inst Tecnol Mat, Valencia, Spain
基金
巴西圣保罗研究基金会;
关键词
tridimensional culture; cell encapsulation; biocompatibility; alginic acid; biomaterial; RELEASE; GROWTH; MICROCAPSULES; ENCAPSULATION; VIABILITY; SYSTEM; REPAIR;
D O I
10.3389/fbioe.2021.674581
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Encapsulation of biological components in hydrogels is a well described method for controlled drug delivery of proteins, tissue engineering and intestinal colonization with beneficial bacteria. Given the potential of tissue engineering in clinical practice, this study aimed to evaluate the feasibility of encapsulation of adipose tissue-derived mesenchymal stem cells (MSCs) of mules in sodium alginate. We evaluated capsule morphology and cell viability, immunophenotype and release after encapsulation. Circular and irregular pores were observed on the hydrogel surface, in which MSCs were present and alive. Capsules demonstrated good capacity of absorption of liquid and cell viability was consistently high through the time points, indicating proper nutrient diffusion. Flow cytometry showed stability of stem cell surface markers, whereas immunohistochemistry revealed the expression of CD44 and absence of MHC-II through 7 days of culture. Stem cell encapsulation in sodium alginate hydrogel is a feasible technique that does not compromise cell viability and preserves their undifferentiated status, becoming a relevant option to further studies of tridimensional culture systems and in vivo bioactive agents delivery.
引用
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页数:10
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