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细胞外基质生物墨水可增强干性,并促进肠类器官的移植,作为一种生物安全的基质胶替代品。

Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative.

作者信息

Xu Zi-Yan, Huang Jin-Jian, Liu Ye, Chen Can-Wen, Qu Gui-Wen, Wang Ge-Fei, Zhao Yun, Wu Xiu-Wen, Ren Jian-An

机构信息

Research Institute of General Surgery, Affiliated Jinling Hospital, Medical School of Nanjing University Nanjing Jiangsu Province China.

School of Medicine, Southeast University Nanjing Jiangsu Province China.

出版信息

Bioeng Transl Med. 2022 Apr 26;8(1):e10327. doi: 10.1002/btm2.10327. eCollection 2023 Jan.

DOI:10.1002/btm2.10327
PMID:36684067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9842023/
Abstract

Organoids hold inestimable therapeutic potential in regenerative medicine and are increasingly serving as an in vitro research platform. Still, their expanding applications are critically restricted by the canonical culture matrix and system. Synthesis of a suitable bioink of bioactivity, biosecurity, tunable stiffness, and printability to replace conventional matrices and fabricate customized culture systems remains challenging. Here, we envisaged a novel bioink formulation based on decellularized extracellular matrix (dECM) from porcine small intestinal submucosa for organoids bioprinting, which provides intestinal stem cells (ISCs) with niche-specific ECM content and biomimetic microstructure. Intestinal organoids cultured in the fabricated bioink exhibited robust generation as well as a distinct differentiation pattern and transcriptomic signature. This bioink established a new co-culture system able to study interaction between epithelial homeostasis and submucosal cells and promote organoids maturation after transplantation into the mesentery of immune-deficient NODSCID-gamma (NSG) mice. In summary, the development of such photo-responsive bioink has the potential to replace tumor-derived Matrigel and facilitate the application of organoids in translational medicine and disease modeling.

摘要

类器官在再生医学中具有不可估量的治疗潜力,并且越来越多地作为体外研究平台。然而,它们不断扩大的应用受到传统培养基质和系统的严重限制。合成一种具有生物活性、生物安全性、可调节硬度和可打印性的合适生物墨水以取代传统基质并制造定制培养系统仍然具有挑战性。在此,我们设想了一种基于猪小肠黏膜下层脱细胞细胞外基质(dECM)的新型生物墨水配方用于类器官生物打印,它为肠道干细胞(ISC)提供特定微环境的细胞外基质成分和仿生微观结构。在制备的生物墨水中培养的肠道类器官表现出强劲的生成以及独特的分化模式和转录组特征。这种生物墨水建立了一种新的共培养系统,能够研究上皮内稳态与黏膜下细胞之间的相互作用,并在移植到免疫缺陷的NOD-SCID-γ(NSG)小鼠肠系膜后促进类器官成熟。总之,这种光响应性生物墨水的开发有可能取代肿瘤来源的基质胶,并促进类器官在转化医学和疾病建模中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/675f6f3968c3/BTM2-8-e10327-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/c4eb5ff74e02/BTM2-8-e10327-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/b8c0fb9e019a/BTM2-8-e10327-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/4f2d0378da55/BTM2-8-e10327-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/63a48299484b/BTM2-8-e10327-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/6d80adc7cbe8/BTM2-8-e10327-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/c2af2b464530/BTM2-8-e10327-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/049844587eae/BTM2-8-e10327-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/d7d3a6185e79/BTM2-8-e10327-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/675f6f3968c3/BTM2-8-e10327-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/c4eb5ff74e02/BTM2-8-e10327-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/b8c0fb9e019a/BTM2-8-e10327-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/4f2d0378da55/BTM2-8-e10327-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/63a48299484b/BTM2-8-e10327-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/6d80adc7cbe8/BTM2-8-e10327-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/c2af2b464530/BTM2-8-e10327-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/049844587eae/BTM2-8-e10327-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/d7d3a6185e79/BTM2-8-e10327-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c479/9842023/675f6f3968c3/BTM2-8-e10327-g009.jpg

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