2019
DOI: 10.1007/s10517-019-04388-1
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Comparative Analysis of Secretome of Human Umbilical Cord- and Bone Marrow-Derived Multipotent Mesenchymal Stromal Cells

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Cited by 20 publications
(9 citation statements)
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“…Compared with BM-MSCs, however, human umbilical cord Wharton's jelly-derived MSCs (hUC-MSCs) offer the advantages of being easily obtained from a routinely discarded tissue without the need of an invasive procedure, having a high harvest rate and exhibiting a greater proliferative activity in vitro [15]. Moreover, BM-MSCs and hUC-MSCs have distinctive transcriptional profiles [16,17] and secretomes [18][19][20]. Although systemic hUC-MSC administration has been widely used in preclinical and clinical studies for other conditions, including ischemic stroke [21], the preclinical efficacy of hUC-MSCs in ICH has so far only been assessed in a few studies.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with BM-MSCs, however, human umbilical cord Wharton's jelly-derived MSCs (hUC-MSCs) offer the advantages of being easily obtained from a routinely discarded tissue without the need of an invasive procedure, having a high harvest rate and exhibiting a greater proliferative activity in vitro [15]. Moreover, BM-MSCs and hUC-MSCs have distinctive transcriptional profiles [16,17] and secretomes [18][19][20]. Although systemic hUC-MSC administration has been widely used in preclinical and clinical studies for other conditions, including ischemic stroke [21], the preclinical efficacy of hUC-MSCs in ICH has so far only been assessed in a few studies.…”
Section: Introductionmentioning
confidence: 99%
“…However, these results were observed in animals and have not been confirmed in clinical studies, despite arguments confirming their predominance [108]. Some studies have confirmed the superiority of UC-MSCs over BM in terms of secretome [109] and migration speed [110]. An evaluation of the expression of 106 cytokines between UCB-derived and UC-derived MSCs showed differences in the excretion of the following: TSP-1, TSG-14, TIMP-1, IL-8, IL-6, CXCL1, GIF, and IGFBP3.…”
Section: Past and Future Perspectivesmentioning
confidence: 85%
“…To further verify the universality of AFSC secretomes and their therapeutic potential, a broader range of donor AFSC should be studied. SCS promote a substantial regenerative effect, and when generated by reproductive stem cells, produce 10 × to 100 × higher SBF concentrations, showing more pronounced therapeutic effects than SCS generated by adult stem cells 35 . SBF released in the AFSC secretome confer immune-modulatory, anti-inflammatory and regenerative properties via the paracrine effect that could be beneficial in cardiovascular applications, and AFSC-S induce dose-dependent angiogenesis and vasculogenesis in ischemic animal models [36][37][38] .…”
Section: Discussionmentioning
confidence: 99%