2014
DOI: 10.1016/j.nano.2014.04.002
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Substrate topography determines the fate of chondrogenesis from human mesenchymal stem cells resulting in specific cartilage phenotype formation

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Cited by 109 publications
(99 citation statements)
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“…Béduer et al [51] hMSC PDMS Micropatterned with striped groove morphology coated with collagen type I Neuronal Biehl et al [52] hESC PDMS Groove Neuronal Lu et al [53] hMSC PCL Nanopillar, nanohole and nanogrill Nanopillar and nanohole topography enhanced Wu et al [54] hNSC PUA Groove and Pillar MSC chondrogenesis and facilitated hyaline cartilage. Neuronal…”
Section: Neuronalmentioning
confidence: 99%
See 1 more Smart Citation
“…Béduer et al [51] hMSC PDMS Micropatterned with striped groove morphology coated with collagen type I Neuronal Biehl et al [52] hESC PDMS Groove Neuronal Lu et al [53] hMSC PCL Nanopillar, nanohole and nanogrill Nanopillar and nanohole topography enhanced Wu et al [54] hNSC PUA Groove and Pillar MSC chondrogenesis and facilitated hyaline cartilage. Neuronal…”
Section: Neuronalmentioning
confidence: 99%
“…This study highlighted that MSC fate in 3D-culture can be controlled even in the absence of differentiation supplements [48] . Table 1 provides the summary of the key research studies highlighting the effect of nanotopographies on directing stem cell fate [49][50][51][52][53][54][55][56] .…”
mentioning
confidence: 99%
“…They can be isolated from various tissues, such as bone marrow and adipose tissue, and comprise a subpopulation that is capable of differentiation towards multiple cell types of the mesodermal lineage including osteocytes, adipocytes, and chondrocytes [22]. It has been suggested that specific surface patterns can either maintain MSCs in an undifferentiated state [23] or drive them towards osteogenic [24], adipogenic [25], or chondrogenic lineages [26]. Cell shape, cytoskeletal tension and RhoA signaling are thought to direct this commitment [27].…”
Section: Introductionmentioning
confidence: 99%
“…Namely, the gene expression of osteocalcin, osteopontin, procollagen type I, alkaline phosphatase, and the transcription factors Runx2 and TGFβ-1 was consistently upregulated only in osteoblastic cells seeded on translationally ordered composite films made by dispersing HAp nanoparticles in a 80 kDa poly(ε-caprolactone) matrix, as opposed to translationally disordered and flat surfaces of the same composition 233 . Many prior studies have shown that topography can be a more important determinant of the viability of the biomaterial/tissue interface than the surface chemistry or stiffness 234,235,236 . This finding has, however, implied that the order at the level of the distribution of topographic features can be a more decisive factor than their surface density, size and geometry.…”
Section: Additional Common Ingredients Of Composite Biomaterialsmentioning
confidence: 99%