Research and Development, Organogenesis Inc., Birmingham, Alabama.
Int Wound J. 2019 Jun;16(3):827-840. doi: 10.1111/iwj.13103. Epub 2019 Mar 10.
The purpose of this study is to characterise the composition of a dehydrated amnion and chorion graft and investigate how factors released from this graft interact with cells important to the wound microenvironment using in vitro models. Characterisation was completed by proteomic analysis of growth factors and cytokines, evaluation of matrix components and protease inhibition, immunohistochemistry, and in vitro release of key growth factors and cytokines. To evaluate the effect of released factors on cells found within the microenvironment, in vitro assays including: cell proliferation, migration, gene expression, protein production, and intracellular pathway activation were used; additionally, responses of fibroblasts in the context of inflammation were measured. We found that released factors from dehydrated amnion/chorion membranes (dACM) stimulated cell proliferation, migration, and altered gene and protein expression profiles of cells important for wound repair in vitro. When cells were cultured in the presence of pro-inflammatory cytokines, the addition of releasate from dACM resulted in an altered production of cytokines, including a reduction of pro-inflammatory regulated on activation, normal T cell expressed and secreted (RANTES). In sum, the results presented here characterise the components of dACM, and in vitro studies were used to evaluate interactions of dACM with cell types important in wound healing.
本研究旨在描述脱水羊膜和绒毛膜移植物的组成,并利用体外模型研究来自该移植物的释放因子如何与对伤口微环境重要的细胞相互作用。通过对生长因子和细胞因子的蛋白质组分析、基质成分和蛋白酶抑制的评估、免疫组织化学以及关键生长因子和细胞因子的体外释放来完成特性描述。为了评估释放因子对微环境中发现的细胞的影响,使用了体外测定法,包括细胞增殖、迁移、基因表达、蛋白质产生和细胞内途径激活;此外,还测量了炎症背景下成纤维细胞的反应。我们发现,脱水羊膜/绒毛膜膜(dACM)释放的因子刺激细胞增殖、迁移,并改变体外伤口修复中重要细胞的基因和蛋白质表达谱。当细胞在促炎细胞因子存在的情况下培养时,dACM 释放物的添加导致细胞因子的产生发生改变,包括促炎调节的激活、正常 T 细胞表达和分泌(RANTES)的减少。总之,这里呈现的结果描述了 dACM 的成分,并且体外研究用于评估 dACM 与伤口愈合中重要的细胞类型的相互作用。