2011
DOI: 10.1016/j.biomaterials.2011.05.092
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Spheroid formation of mesenchymal stem cells on chitosan and chitosan-hyaluronan membranes

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Cited by 198 publications
(221 citation statements)
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“…On the polycationic chitosan membrane, A-MSCs aggregated through noncontrolled cell motility and readily merged to form aggregates, but the size distribution displayed high variability. 71,72 Nanoculture and poly(ethylene glycol)-micropatterned plates promoted homogeneity and increased the viability of BM-MSC aggregates. 34,73 To enhance initial aggregate size homogeneity and cell viability, thermal lifting surface incorporating with endogenous ECMs was also applied to form BM-MSC aggregates.…”
Section: Methods To Generate 3d Msc Aggregatesmentioning
confidence: 99%
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“…On the polycationic chitosan membrane, A-MSCs aggregated through noncontrolled cell motility and readily merged to form aggregates, but the size distribution displayed high variability. 71,72 Nanoculture and poly(ethylene glycol)-micropatterned plates promoted homogeneity and increased the viability of BM-MSC aggregates. 34,73 To enhance initial aggregate size homogeneity and cell viability, thermal lifting surface incorporating with endogenous ECMs was also applied to form BM-MSC aggregates.…”
Section: Methods To Generate 3d Msc Aggregatesmentioning
confidence: 99%
“…34,35,50 Independent of the aggregation method, increased compactness has been reported in aggregates of A-MSC or BM-MSC over the prolonged culture. 5,35,50,61,72 In long-term culture, the proliferation capacity of placental and A-MSC aggregates generated on chitosan membranes was reduced. 71,72 The incorporation of hyaluronan in chitosan membrane increased the survival and proliferation ability presumably due to increased cell migration and matrix synthesis.…”
Section: -115mentioning
confidence: 99%
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“…21,22 DPSCs are an attractive postnatal stem cell source as they are easily accessible, can be easily expanded ex vivo, and exhibit multipotency and regenerative capacity, whereas extraction of MSCs requires an invasive procedure and MSCs exhibit less expansion capacity than do DPSCs. [23][24][25] Murine DPSCs are derived from neural crest origin and express the epithelial-mesenchymal transition (EMT) genes, Twist, Snail, and Slug. 21 These EMT genes have been shown to be important for inhibition of chondrogenesis both in vitro and in vivo, whereas downregulation of EMT genes enhances chondrogenic differentiation.…”
Section: Introductionmentioning
confidence: 99%