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山羊肌腱胶原-人纤维蛋白水凝胶用于基于 HUVEC 微组织的血管生成的全面参数评估。

Goat tendon collagen-human fibrin hydrogel for comprehensive parametric evaluation of HUVEC microtissue-based angiogenesis.

机构信息

Department of Biotechnology, Indian Institute of Technology, Kharagpur, West Bengal, 721302, India.

School of Bio-Sciences and Technology, Centre for Biomaterials Cellular and Molecular Theranostics, Vellore Institute of Technology University, Vellore, Tamil Nadu, 632014, India.

出版信息

Colloids Surf B Biointerfaces. 2018 Mar 1;163:291-300. doi: 10.1016/j.colsurfb.2017.12.056. Epub 2018 Jan 2.

DOI:10.1016/j.colsurfb.2017.12.056
PMID:29329074
Abstract

The cell and extracellular matrix (ECM) interactions play a very important role during angiogenesis. Remodeling of the extracellular matrix along with pro-angiogenic/anti-angiogenic factors, and matrix-degrading proteases, accounts for endothelial cell growth, migration, and tube formation. However, for studying angiogenesis, only limited and expensive biomaterials are available. Despite being biocompatible, inexpensive, and easy availability; the potential of goat tendon collagen (GTC) has never been explored for vascular tissue engineering applications. Hence, the current investigation was focused on evaluating GTC as an alternative matrix for HUVEC microtissue-based angiogenesis. HUVEC microtissues (MTs), synthesized via hanging drop method, were subjected to angiogenesis in GTC-human fibrin (HF) hydrogels. Sprouting tip cells originated from the MTs within 24 h. Further, comprehensive in vitro study and in vivo validation revealed that, endothelial media with FBS and growth factors, 24 h old HUVEC MTs of 500 cells, seeded at 200 aggregates/cm in GTC-HF gel of 100 Pa elastic modulus, resulted in most optimal angiogenesis with intact lumen that was stable up to a week, without any supporting cells. Although early to predict, GTC-HF matrix may serve as a potential ECM for engineering complex and functional tissues of clinical relevance.

摘要

细胞和细胞外基质 (ECM) 的相互作用在血管生成过程中起着非常重要的作用。细胞外基质的重塑以及促血管生成/抗血管生成因子和基质降解蛋白酶,导致内皮细胞的生长、迁移和管腔形成。然而,在研究血管生成时,只有有限的昂贵的生物材料可用。尽管山羊肌腱胶原 (GTC) 具有生物相容性、廉价和易于获得,但它从未被探索用于血管组织工程应用。因此,目前的研究集中在评估 GTC 作为基于 HUVEC 微组织的血管生成的替代基质。通过悬滴法合成的 HUVEC 微组织 (MTs) 在 GTC-人纤维蛋白 (HF) 水凝胶中进行血管生成。在 24 小时内,源自 MT 的发芽尖端细胞出现。此外,全面的体外研究和体内验证表明,内皮培养基中含有 FBS 和生长因子,500 个细胞的 24 小时龄 HUVEC MTs,以 200 个聚集物/cm2 的密度接种在弹性模量为 100Pa 的 GTC-HF 凝胶中,可实现最佳的血管生成,具有完整的管腔,稳定可达一周,无需任何支持细胞。尽管现在预测还为时过早,但 GTC-HF 基质可能成为工程复杂和具有临床相关性的功能性组织的潜在 ECM。

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