Matches in SemOpenAlex for { <https://semopenalex.org/work/W2600180123> ?p ?o ?g. }
- W2600180123 endingPage "835" @default.
- W2600180123 startingPage "826" @default.
- W2600180123 abstract "Hydrogel-based cartilage tissue engineering strategies require the induction and long-term maintenance of adipose derived mesenchymal stem cells (ADMSC) into a stable chondrogenic phenotype. However, ADMSC exhibit the tendency to undergo hypertrophic differentiation, rather than forming permanent hyaline cartilage phenotype changes. This may hinder their implementation in articular cartilage regeneration, but may allow the possibility for bone and bone to soft tissue interface repair. In this study, we examined the effects of hydroxyapatite (HAp) on the chondrogenesis and hypertrophy of ADMSC within bioprinted hyaluronic acid (HA)-based hydrogels. We found that a small amount of HAp (∼10% of polymer concentration) promoted both chondrogenic and hypertrophic differentiation of ADMSC. Increased HAp contents promoted hypertrophic conversion and early osteogenic differentiation of encapsulated ADMSC. Subsequently, ADMSC-laden, stratified constructs with nonmineralized and mineralized layers (i.e., HA based and HA-HAp based) were 3D bioprinted. The constructs were conditioned in chondrogenic medium in either a normoxic or hypoxic environment for 8 weeks to assess the effects of oxygen tension on ADMSC differentiation and interface integration. We further implanted the bioprinted constructs subcutaneously into nude mice for 4 weeks. It was found that hypoxia partially inhibited hypertrophic differentiation by significantly down-regulating the expression of COL10A1, ALP, and MMP13. In addition, hypoxia also suppressed spontaneous calcification of ADMSC and promoted interface integration. This study demonstrates that both HAp content and hypoxia are important to mediate chondrogenesis, hypertrophy, and endochondral ossification of ADMSC. An optimized recipe and condition will allow for 3D bioprinting of multizonal grafts with integrated hard tissue and soft tissue interfaces for the treatment of complex orthopedic defects." @default.
- W2600180123 created "2017-04-07" @default.
- W2600180123 creator A5003930539 @default.
- W2600180123 creator A5016598187 @default.
- W2600180123 creator A5018863416 @default.
- W2600180123 creator A5070577965 @default.
- W2600180123 creator A5074628661 @default.
- W2600180123 date "2017-03-29" @default.
- W2600180123 modified "2023-10-14" @default.
- W2600180123 title "Effects of Hydroxyapatite and Hypoxia on Chondrogenesis and Hypertrophy in 3D Bioprinted ADMSC Laden Constructs" @default.
- W2600180123 cites W1480838859 @default.
- W2600180123 cites W1895404670 @default.
- W2600180123 cites W1970692048 @default.
- W2600180123 cites W1976054112 @default.
- W2600180123 cites W1982423027 @default.
- W2600180123 cites W1985735581 @default.
- W2600180123 cites W2002310197 @default.
- W2600180123 cites W2003576847 @default.
- W2600180123 cites W2014865554 @default.
- W2600180123 cites W2015830031 @default.
- W2600180123 cites W2017894359 @default.
- W2600180123 cites W2021224420 @default.
- W2600180123 cites W2022558287 @default.
- W2600180123 cites W2022712204 @default.
- W2600180123 cites W2025111182 @default.
- W2600180123 cites W2025515198 @default.
- W2600180123 cites W2028422840 @default.
- W2600180123 cites W2032824364 @default.
- W2600180123 cites W2035247102 @default.
- W2600180123 cites W2038857063 @default.
- W2600180123 cites W2039294109 @default.
- W2600180123 cites W2041401385 @default.
- W2600180123 cites W2041708829 @default.
- W2600180123 cites W2046069338 @default.
- W2600180123 cites W2048644480 @default.
- W2600180123 cites W2054711890 @default.
- W2600180123 cites W2068175449 @default.
- W2600180123 cites W2070206697 @default.
- W2600180123 cites W2072288858 @default.
- W2600180123 cites W2077515150 @default.
- W2600180123 cites W2085572225 @default.
- W2600180123 cites W2086542098 @default.
- W2600180123 cites W2087721125 @default.
- W2600180123 cites W2100287997 @default.
- W2600180123 cites W2102525474 @default.
- W2600180123 cites W2109415576 @default.
- W2600180123 cites W2110666890 @default.
- W2600180123 cites W2115728174 @default.
- W2600180123 cites W2145795759 @default.
- W2600180123 cites W2148699117 @default.
- W2600180123 cites W2156622891 @default.
- W2600180123 cites W2159468893 @default.
- W2600180123 cites W2168855290 @default.
- W2600180123 cites W2180957069 @default.
- W2600180123 cites W2253113710 @default.
- W2600180123 cites W2271618911 @default.
- W2600180123 cites W2290631951 @default.
- W2600180123 cites W2307984414 @default.
- W2600180123 cites W2308058717 @default.
- W2600180123 cites W2309305101 @default.
- W2600180123 cites W2313431446 @default.
- W2600180123 cites W2337523494 @default.
- W2600180123 cites W2337961396 @default.
- W2600180123 cites W2376741234 @default.
- W2600180123 cites W2419162533 @default.
- W2600180123 cites W2487381011 @default.
- W2600180123 cites W2500804873 @default.
- W2600180123 cites W2504826727 @default.
- W2600180123 cites W2528088648 @default.
- W2600180123 cites W38879183 @default.
- W2600180123 cites W4249937174 @default.
- W2600180123 doi "https://doi.org/10.1021/acsbiomaterials.7b00101" @default.
- W2600180123 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33440487" @default.
- W2600180123 hasPublicationYear "2017" @default.
- W2600180123 type Work @default.
- W2600180123 sameAs 2600180123 @default.
- W2600180123 citedByCount "39" @default.
- W2600180123 countsByYear W26001801232018 @default.
- W2600180123 countsByYear W26001801232019 @default.
- W2600180123 countsByYear W26001801232020 @default.
- W2600180123 countsByYear W26001801232021 @default.
- W2600180123 countsByYear W26001801232022 @default.
- W2600180123 countsByYear W26001801232023 @default.
- W2600180123 crossrefType "journal-article" @default.
- W2600180123 hasAuthorship W2600180123A5003930539 @default.
- W2600180123 hasAuthorship W2600180123A5016598187 @default.
- W2600180123 hasAuthorship W2600180123A5018863416 @default.
- W2600180123 hasAuthorship W2600180123A5070577965 @default.
- W2600180123 hasAuthorship W2600180123A5074628661 @default.
- W2600180123 hasConcept C105702510 @default.
- W2600180123 hasConcept C108586683 @default.
- W2600180123 hasConcept C136229726 @default.
- W2600180123 hasConcept C178790620 @default.
- W2600180123 hasConcept C17938293 @default.
- W2600180123 hasConcept C185592680 @default.
- W2600180123 hasConcept C189165786 @default.
- W2600180123 hasConcept C198826908 @default.
- W2600180123 hasConcept C2779718196 @default.