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Search for Novel Plasma Membrane Proteins as Potential Biomarkers in Human Mesenchymal Stem Cells Derived from Dental Pulp, Adipose Tissue, Bone Marrow, and Hair Follicle
被引:12
作者:

Akpinar, Gurler
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机构:
Kocaeli Univ, Sch Med, Dept Med Biol, TR-41001 Kocaeli, Turkey Kocaeli Univ, Sch Med, Dept Med Biol, TR-41001 Kocaeli, Turkey

Yoneten, Kubra Karaosmanoglu
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机构:
Kocaeli Univ, Dept Biomed Engn, Technol Fac, TR-41001 Kocaeli, Turkey Kocaeli Univ, Sch Med, Dept Med Biol, TR-41001 Kocaeli, Turkey

论文数: 引用数:
h-index:
机构:

Karaoz, Erdal
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h-index: 0
机构:
Istinye Univ, Dept Histol & Embryol, Sch Med, TR-34010 Istanbul, Turkey Kocaeli Univ, Sch Med, Dept Med Biol, TR-41001 Kocaeli, Turkey
机构:
[1] Kocaeli Univ, Sch Med, Dept Med Biol, TR-41001 Kocaeli, Turkey
[2] Kocaeli Univ, Dept Biomed Engn, Technol Fac, TR-41001 Kocaeli, Turkey
[3] Istinye Univ, Dept Histol & Embryol, Sch Med, TR-34010 Istanbul, Turkey
关键词:
Plasma membrane proteomics;
Mesenchymal stem cell markers;
CDs;
nLC-MS/MS;
QUANTITATIVE PROTEOMICS;
INTERNATIONAL-SOCIETY;
PROGENITOR CELLS;
STROMAL CELLS;
DIFFERENTIATION;
MARKERS;
GENE;
NOMENCLATURE;
EXPRESSION;
CHALLENGES;
D O I:
10.1007/s00232-021-00190-1
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:
One of the drawbacks preventing the use of mesenchymal stem cells (MSCs) in clinical practice is the heterogeneous nature of their cultures. MSC cultures are not homogeneously formed by the MSCs and may contain non-mesenchymal cell types. Therefore, prior to use in clinics or research, complete characterization of MSCs should be performed to demonstrate the existence or absence of proper stem cell markers, many of which are happened to be cell-surface proteins. Unfortunately, the success of MSC characterization studies is limited due to the low specificity of the currently available cell-surface markers. Therefore, in this study, we aimed to investigate the plasma membrane (PM) proteins of MSCs isolated from human dental pulp (DP), adipose tissue (AT), bone marrow (BM), and hair follicle (HF) with the hope of proposing novel putative specific MSC markers. Differential-velocity centrifugation was used to enrich PM proteins. The isolated proteins were then identified by nLC-MS/MS and subjected to bioinformatics analysis. Proteins that were unique to each MSC type (CD9, CD10, CD63 for DP-MSCs; CD26, CD81, CD201, CD364 for AT-MSCs; Cd49a, CD49d for HF-MSCs; CD49e, CD56, CD92, CD97, CD156b, CD156c, CD220, CD221, CD298, CD315 for BM-MSCs) and common to all four MSC types (CD13, CD29, CD44, CD51, CD59, CD73, CD90) were identified. Uncharacterized proteins that have transmembrane (TM) domains were also detected. Some of the proteins identified in this study were the putative cell-surface markers that might be used for characterization of MSCs.
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页码:409 / 422
页数:14
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Ravau, Joachim
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Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium

Andre, Floriane
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Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium

Najimi, Mustapha
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Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium

Sokal, Etienne
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Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium

Lombard, Catherine
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Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium Catholic Univ Louvain, IREC, Lab Pediat Hepatol & Cell Therapy, Ave Mounier 52, B-1200 Brussels, Belgium