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Human tendon cell response to 7 commercially available extracellular matrix materials: an in vitro study.

机译:人类肌腱细胞反应7商业可用的细胞外基质材料:一个体外研究。

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摘要

PURPOSE: To evaluate the response of human tenocytes in culture to 7 commercially available extracellular matrix (ECM) patches. METHODS: Four samples of each ECM were incubated in human tenocyte cultures by use of standard methods. Cell adhesion, cell proliferation, and cellular production of type I and type III collagen, decorin, and scleraxis were measured for each sample according to established experimental methods. Histologic samples were examined to measure the migration of the tenocytes into the ECM. RESULTS: Tenocytes adhered more to samples of layered submucosal pig intestine than the 6 other ECM materials (P < .002). Tenocytes proliferated more and produced more matrix proteins when cultured on ECM derived from unaltered dermal specimens of human or porcine origin (P < .001). Cells were not seen to have migrated into the matrix of any ECM sample. CONCLUSIONS: Human tenocytes reacted most favorably to dermal ECM samples that were not chemically cross-linked by the manufacturer. Less favorable responses of the human cells were seen when cultured with equine or synthetic ECM, which showed favorable biologic responses in nonhuman models. Cellular migration into the matrix of the ECM is a complex process and cannot be replicated in this model entirely. CLINICAL RELEVANCE: The results of this study suggest that dermal ECM may more favorably react with human tendon tissue than ECM of other origins. This may have great relevance as research continues in the field of augmenting surgical soft-tissue repair.
机译:目的:评价人类的反应tenocytes文化7商用细胞外基质(ECM)补丁。每个ECM在人工孵化的样本tenocyte文化通过使用标准的方法。细胞粘附、细胞增殖和细胞我型和III型胶原蛋白的生产,decorin, scleraxis测量根据建立的实验样品方法。测量tenocytes迁移到ECM。分层的猪小肠粘膜下比6其他ECM材料(P < .002)。扩散和产生更多的矩阵当培养在ECM来自蛋白质不变的人类或猪的皮肤标本起源(P <措施)。迁移到任何ECM的矩阵样本。结论:人类tenocytes反应最多顺利地没有真皮基质的样品化学交联的制造商。有利的反应的人类细胞当用马或合成ECM培养显示良好的非人类的生物反应模型。ECM是一个复杂的过程,不能被复制在这个模型中。本研究的结果表明,真皮基质更顺利地与人体肌腱组织反应比其他ECM的起源。相关领域的研究仍在继续增加手术软组织修复。

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