TMT-Based Quantitative Proteomics Analysis Reveals Differentially Expressed Proteins between Different Sources of hMSCs

被引:0
作者
Naudot, Marie [1 ]
Le Ber, Julie [2 ]
Marcelo, Paulo [3 ]
机构
[1] Univ Picardie Jules Verne, UR7516, Chirurg IMagerie & REgenerat Tissulaire Extremite, F-80039 Amiens, France
[2] Univ Picardie Jules Verne, PLATANN, F-80039 Amiens, France
[3] Univ Picardie Jules Verne, Plateforme Ingn Cellulaire & Anal Prot ICAP, CNRS, FR 3085,ICP, F-80039 Amiens, France
关键词
mesenchymal stem cells; proteomics; tissue engineering; regenerative medicine; MESENCHYMAL STEM-CELLS; BONE-MARROW; ADIPOSE-TISSUE; STROMAL CELLS; DENTAL-PULP; TRANSPLANTATION; INFLAMMATION; ORIGIN;
D O I
10.3390/ijms241713544
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cells (MSCs) are an attractive therapeutic tool for tissue engineering and regenerative medicine owing to their regenerative and trophic properties. The best-known and most widely used are bone marrow MSCs, which are currently being harvested and developed from a wide range of adult and perinatal tissues. MSCs from different sources are believed to have different secretion potentials and production, which may influence their therapeutic effects. To confirm this, we performed a quantitative proteomic analysis based on the TMT technique of MSCs from three different sources: Wharton's jelly (WJ), dental pulp (DP), and bone marrow (BM). Our analysis focused on MSC biological properties of interest for tissue engineering. We identified a total of 611 differentially expressed human proteins. WJ-MSCs showed the greatest variation compared with the other sources. WJ produced more extracellular matrix (ECM) proteins and ECM-affiliated proteins and proteins related to the inflammatory and immune response processes. BM-MSCs expressed more proteins involved in osteogenic, adipogenic, neuronal, or muscular differentiation and proteins involved in paracrine communication. Compared to the other sources, DP-MSCs overexpressed proteins involved in the exocytosis process. The results obtained confirm the existence of differences between WJ, DP, and BM-MSCs and the need to select the MSC origin according to the therapeutic objective sought.
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页数:16
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