2015
DOI: 10.2460/ajvr.76.9.814
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Comparison of the characteristics and multipotential and in vivo cartilage formation capabilities between porcine adipose-derived stem cells and porcine skin-derived stem cell–like cells

Abstract: Results suggested that pSSCs may be a viable alternative to pASCs as a source of progenitor cells for tissue engineering in regenerative medicine.

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Cited by 4 publications
(5 citation statements)
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“…7,28,29 These include comparable morphology, proliferative capacity, alkaline phosphatase activity, cell surface marker expression, metabolic pathways, biologic functions, and transcription factors. 10,23,30 pASCs have often been compared side-by-side with porcine stem cells from these other tissue sources, revealing characteristics and comparable multilineage differentiation abilities as well. 9,23,28 While knowledge of the differentiation abilities of pASCs is currently limited to a few reports, porcine bone marrow-derived stem cells (pBMSCs) have been differentiated into myocytes, 31 endothelial cells, 32 and epithelial cells.…”
Section: Multilineage Differentiation Abilitiesmentioning
confidence: 99%
“…7,28,29 These include comparable morphology, proliferative capacity, alkaline phosphatase activity, cell surface marker expression, metabolic pathways, biologic functions, and transcription factors. 10,23,30 pASCs have often been compared side-by-side with porcine stem cells from these other tissue sources, revealing characteristics and comparable multilineage differentiation abilities as well. 9,23,28 While knowledge of the differentiation abilities of pASCs is currently limited to a few reports, porcine bone marrow-derived stem cells (pBMSCs) have been differentiated into myocytes, 31 endothelial cells, 32 and epithelial cells.…”
Section: Multilineage Differentiation Abilitiesmentioning
confidence: 99%
“…Cells from each pig were cultured separately and passaged once or twice with culture medium changed every two days. MSC characteristics of pSSCs were confirmed by fluorescence-activated cell sorting analysis as described previously [10].…”
Section: Methodsmentioning
confidence: 99%
“…For analysis of adipocytes generated during osteogenic differentiation, ORO staining and quantification were conducted as described previously [10]. Briefly, pSSCs were stained with a 0.6% ORO (Sigma-Aldrich) solution (w/v) for 1 h at room temperature.…”
Section: Methodsmentioning
confidence: 99%
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“…In mammals, WAT depots occupy different anatomical locations and demonstrate morphological and functional heterogeneity [26]. In the pig, abdominal and dorsal regions of subcutaneous fat have been the most frequently used source of ASCs [27][28][29][30]. There is only one report that refers to the caudal part of the body for ASC isolation [31].…”
Section: Basic Biology Of Ascs Isolated From Livestockmentioning
confidence: 99%