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用于体外和体内应用的人心脏组织向细胞外基质自组装水凝胶的加工

Processing of Human Cardiac Tissue Toward Extracellular Matrix Self-assembling Hydrogel for In Vitro and In Vivo Applications.

作者信息

Becker Matthias, Maring Janita A, Oberwallner Barbara, Kappler Benjamin, Klein Oliver, Falk Volkmar, Stamm Christof

机构信息

Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health; Berlin-Brandenburg Center for Regenerative Therapies (BCRT).

Berlin-Brandenburg Center for Regenerative Therapies (BCRT).

出版信息

J Vis Exp. 2017 Dec 4(130):56419. doi: 10.3791/56419.

Abstract

Acellular extracellular matrix preparations are useful for studying cell-matrix interactions and facilitate regenerative cell therapy applications. Several commercial extracellular matrix products are available as hydrogels or membranes, but these do not possess tissue-specific biological activity. Because perfusion decellularization is usually not possible with human heart tissue, we developed a 3-step immersion decellularization process. Human myocardial slices procured during surgery are first treated with detergent-free hyperosmolar lysis buffer, followed by incubation with the ionic detergent, sodium dodecyl sulfate, and the process is completed by exploiting the intrinsic DNase activity of fetal bovine serum. This technique results in cell-free sheets of cardiac extracellular matrix with largely preserved fibrous tissue architecture and biopolymer composition, which were shown to provide specific environmental cues to cardiac cell populations and pluripotent stem cells. Cardiac extracellular matrix sheets can then be further processed into a microparticle powder without further chemical modification, or, via short-term pepsin digestion, into a self-assembling cardiac extracellular matrix hydrogel with preserved bioactivity.

摘要

去细胞细胞外基质制剂可用于研究细胞与基质的相互作用,并促进再生细胞治疗的应用。有几种商业细胞外基质产品以水凝胶或膜的形式提供,但这些产品不具备组织特异性生物活性。由于人心脏组织通常无法进行灌注去细胞处理,我们开发了一种三步浸泡去细胞处理方法。手术中获取的人心肌切片首先用不含洗涤剂的高渗裂解缓冲液处理,然后与离子洗涤剂十二烷基硫酸钠一起孵育,该过程通过利用胎牛血清的内在DNase活性来完成。该技术产生了无细胞的心脏细胞外基质片,其纤维组织结构和生物聚合物组成在很大程度上得以保留,这些基质片被证明能为心脏细胞群体和多能干细胞提供特定的环境线索。然后,心脏细胞外基质片可以在不进行进一步化学修饰的情况下进一步加工成微粒粉末,或者通过短期胃蛋白酶消化,加工成具有保留生物活性的自组装心脏细胞外基质水凝胶。

相似文献

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The cytoprotective capacity of processed human cardiac extracellular matrix.加工后的人心脏细胞外基质的细胞保护能力。
J Mater Sci Mater Med. 2016 Jul;27(7):120. doi: 10.1007/s10856-016-5730-5. Epub 2016 Jun 7.

本文引用的文献

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The cytoprotective capacity of processed human cardiac extracellular matrix.加工后的人心脏细胞外基质的细胞保护能力。
J Mater Sci Mater Med. 2016 Jul;27(7):120. doi: 10.1007/s10856-016-5730-5. Epub 2016 Jun 7.

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