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基于工程化硫酸化多糖和丝素蛋白的可注射 IPN 水凝胶,具有增强和生长因子呈现能力,用于软骨组织工程。

Engineering sulfated polysaccharides and silk fibroin based injectable IPN hydrogels with stiffening and growth factor presentation abilities for cartilage tissue engineering.

机构信息

Department of Biological Sciences and Bioengineering, Indian Institute of Technology-Kanpur, Kanpur-208016, Uttar Pradesh, India.

The Mehta Family Centre for Engineering in Medicine, Indian Institute of Technology-Kanpur, Kanpur-208016, Uttar Pradesh, India.

出版信息

Biomater Sci. 2024 Apr 16;12(8):2067-2085. doi: 10.1039/d3bm01466e.

Abstract

The extracellular matrix (ECM) presents a framework for various biological cues and regulates homeostasis during both developing and mature stages of tissues. During development of cartilage, the ECM plays a critical role in endowing both biophysical and biochemical cues to the progenitor cells. Hence, designing microenvironments that recapitulate these biological cues as provided by the ECM during development may facilitate the engineering of cartilage tissue. In the present study, we fabricated an injectable interpenetrating hydrogel (IPN) system which serves as an artificial ECM and provides chondro-inductive niches for the differentiation of stem cells to chondrocytes. The hydrogel was designed to replicate the gradual stiffening (as a biophysical cue) and the presentation of growth factors (as a biochemical cue) as provided by the natural ECM of the tissue, thus exemplifying a biomimetic approach. This dynamic stiffening was achieved by incorporating silk fibroin, while the growth factor presentation was accomplished using sulfated-carboxymethyl cellulose. Silk fibroin and sulfated-carboxymethyl cellulose (s-CMC) were combined with tyraminated-carboxymethyl cellulose (t-CMC) and crosslinked using HRP/HO to fabricate s-CMC/t-CMC/silk IPN hydrogels. Initially, the fabricated hydrogel imparted a soft microenvironment to promote chondrogenic differentiation, and with time it gradually stiffened to offer mechanical support to the joint. Additionally, the presence of s-CMC conferred the hydrogel with the property of sequestering cationic growth factors such as TGF-β and allowing their prolonged presentation to the cells. More importantly, TGF-β loaded in the developed hydrogel system remained active and induced chondrogenic differentiation of stem cells, resulting in the deposition of cartilage ECM components which was comparable to the hydrogels that were treated with TGF-β provided through media. Overall, the developed hydrogel system acts as a reservoir of the necessary biological cues for cartilage regeneration and simultaneously provides mechanical support for load-bearing tissues such as cartilage.

摘要

细胞外基质 (ECM) 为各种生物线索提供了一个框架,并在组织的发育和成熟阶段调节其动态平衡。在软骨发育过程中,ECM 对于向祖细胞提供生物物理和生化线索起着至关重要的作用。因此,设计能够再现 ECM 在发育过程中提供的这些生物线索的微环境可能有助于软骨组织的工程化。在本研究中,我们制备了一种可注射的互穿水凝胶 (IPN) 系统,该系统充当人工 ECM,并为干细胞向软骨细胞的分化提供了软骨诱导龛。该水凝胶的设计旨在复制逐渐变硬(作为生物物理线索)和生长因子的呈现(作为生化线索),这与组织的天然 ECM 提供的线索相类似,因此是一种仿生方法。这种动态变硬是通过掺入丝素蛋白来实现的,而生长因子的呈现是通过使用硫酸化羧甲基纤维素来实现的。丝素蛋白和硫酸化羧甲基纤维素 (s-CMC) 与接枝酪氨酸羧甲基纤维素 (t-CMC) 结合,并使用 HRP/HO 交联,以制备 s-CMC/t-CMC/丝素 IPN 水凝胶。最初,所制备的水凝胶赋予软微环境以促进软骨分化,随着时间的推移,它逐渐变硬,为关节提供机械支撑。此外,s-CMC 的存在赋予水凝胶隔离阳离子生长因子(如 TGF-β)的特性,并允许其向细胞进行长时间呈现。更重要的是,负载在开发的水凝胶系统中的 TGF-β 保持活性,并诱导干细胞的软骨分化,导致软骨 ECM 成分的沉积,其与通过介质处理的 TGF-β 处理的水凝胶相当。总的来说,所开发的水凝胶系统充当软骨再生所需的必要生物线索的储存库,同时为软骨等承重组织提供机械支撑。

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