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通过纳米液相色谱-质谱联用分析对无膜干细胞成分进行蛋白质组分析及其抗炎活性

Proteome Profiling of Membrane-Free Stem Cell Components by Nano-LS/MS Analysis and Its Anti-Inflammatory Activity.

作者信息

Venkatarame Gowda Saralamma Venu, Vetrivel Preethi, Kim Seong Min, Ha Sang Eun, Lee Ho Jeong, Lee Sang Joon, Kim Young Sil, Pak Jung Eun, Lee Hye Jin, Heo Jeong Doo, Kim Gon Sup

机构信息

Research Institute of Life Science and College of Veterinary Medicine, Gyeongsang National University, 501 Jinju-daero, Jinju, Gyeongnam 52828, Republic of Korea.

Gyeongnam Department of Environment Toxicology and Chemistry, Toxicity Screening Research Center, Korea Institute of Toxicology, 17 Jegok-gil, Munsan-eup, Jinju, Gyeongnam 52834, Republic of Korea.

出版信息

Evid Based Complement Alternat Med. 2019 Nov 4;2019:4683272. doi: 10.1155/2019/4683272. eCollection 2019.

Abstract

The use of adipose-derived stem cells (ADSCs) to enhance wound healing and tissue regeneration is progressively being accepted. Proteomic profiling of cultured ADSCs by mass spectrometry (MS) is a valuable tool to determine the identity of the proteins involved in multiple pathways, which make these ADSCs unique. In the current study, Nano-LC-MS/MS analysis was implemented on the membrane-free stem cell component (MFSCC), and the MS analysis revealed the presence of 252 proteins, that are involved in several biological functions, like metabolic process, biological regulation, developmental process, cell proliferation, and many more. Furthermore, bioinformatic analyses of the identified proteins in MFSCC found them to be involved in versatile pathways, like integrin pathway and wound healing response-related pathways. In addition, we also investigated the anti-inflammatory effects of MFSCC on lipopolysaccharide (LPS) stimulated mouse macrophage (RAW264.7) cells. The cell cytotoxicity of MFSCC was measured using MTT and LDH assays, the production of nitric oxide (NO) was measured by the Griess assay, and the protein expression levels of inducible nitric oxide (iNOS) and cyclooxygenase (COX-2) were examined by western blot analysis. The results showed that MFSCC concentrations ranging from 0.1 to 3 g/mL did not show any significant cytotoxicity in LPS-induced RAW264.7 cells. Treatment with MFSCC of LPS-stimulated RAW264.7 cells significantly suppressed the production of NO and the expression of iNOS and COX-2 proteins related to inflammation. The present findings lead to a better understanding of the therapeutic potential of MFSCC and strongly promote it for the future clinical development of novel non-cell-based stem cell therapeutics.

摘要

使用脂肪来源干细胞(ADSCs)促进伤口愈合和组织再生正逐渐被接受。通过质谱(MS)对培养的ADSCs进行蛋白质组分析是确定参与多种途径的蛋白质身份的宝贵工具,这些途径使这些ADSCs具有独特性。在本研究中,对无膜干细胞成分(MFSCC)进行了纳升级液相色谱-串联质谱(Nano-LC-MS/MS)分析,MS分析显示存在252种蛋白质,它们参与多种生物学功能,如代谢过程、生物调节、发育过程、细胞增殖等等。此外,对MFSCC中鉴定出的蛋白质进行生物信息学分析发现它们参与多种途径,如整合素途径和伤口愈合反应相关途径。此外,我们还研究了MFSCC对脂多糖(LPS)刺激的小鼠巨噬细胞(RAW264.7)细胞的抗炎作用。使用MTT和LDH测定法测量MFSCC的细胞毒性,通过Griess测定法测量一氧化氮(NO)的产生,并通过蛋白质印迹分析检测诱导型一氧化氮合酶(iNOS)和环氧化酶(COX-2)的蛋白质表达水平。结果表明,浓度范围为0.1至3 g/mL的MFSCC在LPS诱导的RAW264.7细胞中未显示出任何显著的细胞毒性。用MFSCC处理LPS刺激的RAW264.7细胞可显著抑制NO的产生以及与炎症相关的iNOS和COX-2蛋白的表达。本研究结果有助于更好地理解MFSCC的治疗潜力,并有力地推动其在新型非细胞型干细胞疗法未来临床开发中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e79/6875034/bea3a124f6e0/ECAM2019-4683272.001.jpg

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