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角质形成细胞诱导间充质干细胞分化为真皮成肌纤维细胞:在有效伤口愈合中的作用

Keratinocyte Induced Differentiation of Mesenchymal Stem Cells into Dermal Myofibroblasts: A Role in Effective Wound Healing.

作者信息

Mishra Pravin J, Mishra Prasun J, Banerjee Debabrata

机构信息

Intermountain Precision Genomics, Intermountain Healthcare, Dixie Regional Medical Center 292 South 1470 East, Suite 201 & 301, St. George, UT 84770, USA.

Department of Biochemical and Cellular Pharmacology, Genentech, 1, DNA Way, South San Francisco, California 94080, USA.

出版信息

Int J Transl Sci. 2016 Jan;2016(1):5-32. doi: 10.13052/ijts2246-8765.2016.002.

Abstract

We have previously demonstrated that human mesenchymal stem cells (hMSCs) migrate toward human keratinocytes as well as toward conditioned medium from cultured human keratinocytes (KCM) indicating that the hMSCs respond to signals from keratinocytes [1]. Using fluorescently labeled cells we now show that hMSCs appear to surround keratinocytes, and this organization is recapitulated . Incubation of hMSCs with KCM induced dermal myofibroblast like differentiation characterized by expression of cytoskeletal markers and increased expression of cytokines including SDF-1, IL-8, IL-6 and CXCL5. Interaction of keratinocytes with hMSCs appears to be important in the wound healing process. Therapeutic efficacy of hMSCs in wound healing was examined in two animal models representing normal and chronic wound healing. Accelerated wound healing was observed when hMSCs and KCM exposed hMSCs (KCMSCs) were injected near wound site in nude and NOD/SCID mice. Long term follow up of wound healing revealed that in the hMSC treated wounds there was little evidence of residual scarring. These dermal myofibroblast like hMSCs add to the wound healing process. Together, the keratinocyte and hMSCs morphed dermal myofibroblast like cells as well as the factors secreted by these cells support wound healing with minimal scarring. The ability of hMSCs to support wound healing process represents another striking example of the importance of keratinocyte and hMSCs interplay in the wound microenvironment resulting in effective wound healing with minimal scarring.

摘要

我们之前已经证明,人间充质干细胞(hMSCs)会向人角质形成细胞迁移,也会向培养的人角质形成细胞的条件培养基(KCM)迁移,这表明hMSCs会对来自角质形成细胞的信号作出反应[1]。现在我们使用荧光标记细胞表明,hMSCs似乎会包围角质形成细胞,并且这种组织形式得以重现。将hMSCs与KCM共同孵育会诱导其向真皮肌成纤维细胞样分化,其特征为细胞骨架标志物的表达以及包括SDF-1、IL-8、IL-6和CXCL5在内的细胞因子表达增加。角质形成细胞与hMSCs的相互作用在伤口愈合过程中似乎很重要。在代表正常和慢性伤口愈合的两种动物模型中检测了hMSCs在伤口愈合中的治疗效果。当将hMSCs和经KCM处理的hMSCs(KCMSCs)注射到裸鼠和NOD/SCID小鼠的伤口部位附近时,观察到伤口愈合加速。对伤口愈合的长期随访显示,在接受hMSCs治疗的伤口中,几乎没有残留瘢痕的迹象。这些真皮肌成纤维细胞样的hMSCs促进了伤口愈合过程。总之,角质形成细胞和hMSCs转变而来的真皮肌成纤维细胞样细胞以及这些细胞分泌的因子支持了伤口愈合,且瘢痕形成最少。hMSCs支持伤口愈合过程的能力代表了角质形成细胞与hMSCs在伤口微环境中相互作用的重要性的另一个显著例子,从而实现了有效的伤口愈合且瘢痕形成最少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3171/4902180/cb8892ad6683/nihms785579f1a.jpg

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