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将细胞活性因子固定于伤口床可促进愈合。

Anchoring a cytoactive factor in a wound bed promotes healing.

作者信息

Chattopadhyay Sayani, Guthrie Kathleen M, Teixeira Leandro, Murphy Christopher J, Dubielzig Richard R, McAnulty Jonathan F, Raines Ronald T

机构信息

Department of Chemistry, University of Wisconsin-Madison, WI, USA.

Department of Surgical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, WI, USA.

出版信息

J Tissue Eng Regen Med. 2016 Dec;10(12):1012-1020. doi: 10.1002/term.1886. Epub 2014 Mar 27.

Abstract

Wound healing is a complex process that requires the intervention of cytoactive factors. The one-time application of soluble factors to a wound bed does not maintain a steady, sufficient concentration. Here we investigated the benefits of anchoring a factor in a wound bed via a tether to endogenous collagen. We used a collagen-mimetic peptide (CMP) as a pylon. The CMP binds to damaged but not intact collagen and thus localizes a pendant cytoactive factor in the regions of a wound bed that require intervention. As a model factor, we chose substance P, a peptide of the tachykinin family that promotes wound healing. Using splinted wounds in db/db mice, we found that the one-time application of a CMP-substance P conjugate enhances wound healing compared to unconjugated substance P and other controls. Specifically, all 16 wounds treated with the conjugate closed more thoroughly and, did so with extensive re-epithelialization and mitigated inflammatory activity. These data validate a simple and general strategy for re-engineering wound beds by the integration of beneficial cytoactive factors. Copyright © 2014 John Wiley & Sons, Ltd.

摘要

伤口愈合是一个复杂的过程,需要细胞活性因子的干预。将可溶性因子一次性应用于伤口床并不能维持稳定、足够的浓度。在此,我们研究了通过与内源性胶原蛋白相连的方式将一种因子固定在伤口床中的益处。我们使用一种胶原模拟肽(CMP)作为支柱。CMP与受损而非完整的胶原蛋白结合,从而将一种悬垂的细胞活性因子定位在伤口床中需要干预的区域。作为模型因子,我们选择了P物质,它是速激肽家族的一种促进伤口愈合的肽。使用db/db小鼠的夹板伤口,我们发现与未结合的P物质及其他对照相比,一次性应用CMP-P物质缀合物可增强伤口愈合。具体而言,用该缀合物处理的所有16个伤口愈合得更彻底,且伴有广泛的重新上皮化和减轻的炎症活动。这些数据验证了一种通过整合有益的细胞活性因子对伤口床进行重新构建的简单通用策略。版权所有© 2014约翰威立父子有限公司。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e89/4219926/141fb676df0e/nihms-592361-f0001.jpg

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