2013
DOI: 10.1016/j.jcyt.2012.11.009
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Mesenchymal stromal/stem cells markers in the human bone marrow

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Cited by 100 publications
(96 citation statements)
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“…These cells were found to represent a heterogeneous cell population, most of them constitutively expressing PDGFR and CD10 but variably expressing alpha-SMA, c-kit, Oct4 and CD68 [40]. The expression of CD10 in MSCs was reported either positive, or negative [5,14,22,28,33]. In the present study, the CD10 expression in the mammary samples was heterogeneous, positive or negative, as compared with the homogenous expression of CD34.…”
Section: Discussionmentioning
confidence: 41%
“…These cells were found to represent a heterogeneous cell population, most of them constitutively expressing PDGFR and CD10 but variably expressing alpha-SMA, c-kit, Oct4 and CD68 [40]. The expression of CD10 in MSCs was reported either positive, or negative [5,14,22,28,33]. In the present study, the CD10 expression in the mammary samples was heterogeneous, positive or negative, as compared with the homogenous expression of CD34.…”
Section: Discussionmentioning
confidence: 41%
“…In the human bone and BM, which are currently a major source for MSC therapeutics (table 1), MSC subpopulations, such as fibroblastoid reticular stromal cells, adipose stromal cells, round stromal cells and bone lining cells, reside in distinct microanatomical localizations [30]. In addition, the perivascular niche harbors cells featuring MSC phenotypes as shown for various organs [4,30,31].…”
Section: The Heterogeneity Of Mscs and Non-standardized Ex Vivo Cultumentioning
confidence: 99%
“…In addition, the perivascular niche harbors cells featuring MSC phenotypes as shown for various organs [4,30,31]. Due to the low frequency of MSCs in the BM (below 0.1% of nucleated cells [32]), manufacturing substantial numbers of MSC doses for therapeutic applications requires isolation/enrichment of MSCs as well as their in vitro expansion.…”
Section: The Heterogeneity Of Mscs and Non-standardized Ex Vivo Cultumentioning
confidence: 99%
“…It is also expressed abundantly in retinoblastoma tumour cells, so it was used as a suitable marker for identification of suspicious tumour cells in the bone marrow or cerebrospinal fluid of affected patients (Seeger 2011;Laurent et al 2013). However, low levels of GD2 expression in some normal tissues such as the peripheral nerves, neurons (Mennel et al 1992), skin melanocytes (Hersey 1991) and bone marrow stem cells (Rasini et al 2013) limit the widespread use of this antigen for delivering targeted therapy to the eye because of anticipated toxicity, as evident when used for immunotherapy of neuroblastoma (Sorkin et al 2010).…”
Section: Introductionmentioning
confidence: 99%