Matches in SemOpenAlex for { <https://semopenalex.org/work/W2076609872> ?p ?o ?g. }
- W2076609872 endingPage "467" @default.
- W2076609872 startingPage "459" @default.
- W2076609872 abstract "Abstract Diabetic retinopathy is characterized by progressive vascular dropout with subsequent vision loss. We have recently shown that an intravitreal injection of adipose-derived stem cells (ASCs) can stabilize the retinal microvasculature, enabling repair and regeneration of damaged capillary beds in vivo. Because an understanding of ASC status from healthy versus diseased donors will be important as autologous cellular therapies are developed for unmet clinical needs, we took advantage of the hyperglycemic Akimba mouse as a preclinical in vivo model of diabetic retinopathy in an effort aimed at evaluating therapeutic efficacy of adipose-derived stem cells (mASCs) derived either from healthy, nondiabetic or from diabetic mice. To these ends, Akimba mice received intravitreal injections of media conditioned by mASCs or mASCs themselves, subsequent to development of substantial retinal capillary dropout. mASCs from healthy mice were more effective than diabetic mASCs in protecting the diabetic retina from further vascular dropout. Engrafted ASCs were found to preferentially associate with the retinal vasculature. Conditioned medium was unable to recapitulate the vasoprotection seen with injected ASCs. In vitro diabetic ASCs showed decreased proliferation and increased apoptosis compared with healthy mASCs. Diabetic ASCs also secreted less vasoprotective factors than healthy mASCs, as determined by high-throughput enzyme-linked immunosorbent assay. Our findings suggest that diabetic ASCs are functionally impaired compared with healthy ASCs and support the utility of an allogeneic injection of ASCs versus autologous or conditioned media approaches in the treatment of diabetic retinopathy. Significance This work addresses the therapeutic potential of stem cells that are obtained from diabetic donors, and the clinical focus of our work is diabetic retinopathy. This work examined how injected murine adipose-derived stem cells (ASCs) affect the retinal microvasculature in a mouse model of diabetic retinopathy. Results show that ASCs obtained from healthy mice secrete angiogenic growth factors and promote retinal vascular stability when they are injected intravitreally. The findings further suggest that ASCs obtained from diabetic mice have a diminished ability to support the retinal vasculature in this mouse model of retinal vasculopathy." @default.
- W2076609872 created "2016-06-24" @default.
- W2076609872 creator A5006690579 @default.
- W2076609872 creator A5010100874 @default.
- W2076609872 creator A5016211526 @default.
- W2076609872 creator A5017480661 @default.
- W2076609872 creator A5020137042 @default.
- W2076609872 creator A5025486151 @default.
- W2076609872 creator A5032886347 @default.
- W2076609872 creator A5034594283 @default.
- W2076609872 creator A5052313487 @default.
- W2076609872 creator A5055963262 @default.
- W2076609872 creator A5063928870 @default.
- W2076609872 creator A5077822196 @default.
- W2076609872 date "2015-03-13" @default.
- W2076609872 modified "2023-10-15" @default.
- W2076609872 title "Adipose-Derived Stem Cells From Diabetic Mice Show Impaired Vascular Stabilization in a Murine Model of Diabetic Retinopathy" @default.
- W2076609872 cites W1605777639 @default.
- W2076609872 cites W1960543022 @default.
- W2076609872 cites W1964626979 @default.
- W2076609872 cites W1964818565 @default.
- W2076609872 cites W1968625953 @default.
- W2076609872 cites W1971376911 @default.
- W2076609872 cites W1971481846 @default.
- W2076609872 cites W1979274462 @default.
- W2076609872 cites W1995830850 @default.
- W2076609872 cites W1997720046 @default.
- W2076609872 cites W2000229809 @default.
- W2076609872 cites W2005943573 @default.
- W2076609872 cites W2011745548 @default.
- W2076609872 cites W2019780808 @default.
- W2076609872 cites W2021010305 @default.
- W2076609872 cites W2027605832 @default.
- W2076609872 cites W2029624973 @default.
- W2076609872 cites W2030758264 @default.
- W2076609872 cites W2039284766 @default.
- W2076609872 cites W2041386692 @default.
- W2076609872 cites W2052813707 @default.
- W2076609872 cites W2060550658 @default.
- W2076609872 cites W2071671229 @default.
- W2076609872 cites W2074661784 @default.
- W2076609872 cites W2076724486 @default.
- W2076609872 cites W2086411318 @default.
- W2076609872 cites W2086812792 @default.
- W2076609872 cites W2095132685 @default.
- W2076609872 cites W210264929 @default.
- W2076609872 cites W2109879260 @default.
- W2076609872 cites W2115284469 @default.
- W2076609872 cites W2121431403 @default.
- W2076609872 cites W2137602698 @default.
- W2076609872 cites W2138589210 @default.
- W2076609872 cites W2138811791 @default.
- W2076609872 cites W2140005424 @default.
- W2076609872 cites W2144202926 @default.
- W2076609872 cites W2144829538 @default.
- W2076609872 cites W2146479244 @default.
- W2076609872 cites W2152442991 @default.
- W2076609872 cites W2152711442 @default.
- W2076609872 cites W2153008086 @default.
- W2076609872 cites W2153096281 @default.
- W2076609872 cites W2158103340 @default.
- W2076609872 cites W2162883084 @default.
- W2076609872 cites W2164575981 @default.
- W2076609872 cites W2173497140 @default.
- W2076609872 cites W2605187236 @default.
- W2076609872 cites W2616361514 @default.
- W2076609872 doi "https://doi.org/10.5966/sctm.2014-0108" @default.
- W2076609872 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4414213" @default.
- W2076609872 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/25769654" @default.
- W2076609872 hasPublicationYear "2015" @default.
- W2076609872 type Work @default.
- W2076609872 sameAs 2076609872 @default.
- W2076609872 citedByCount "39" @default.
- W2076609872 countsByYear W20766098722016 @default.
- W2076609872 countsByYear W20766098722017 @default.
- W2076609872 countsByYear W20766098722018 @default.
- W2076609872 countsByYear W20766098722019 @default.
- W2076609872 countsByYear W20766098722020 @default.
- W2076609872 countsByYear W20766098722021 @default.
- W2076609872 countsByYear W20766098722022 @default.
- W2076609872 countsByYear W20766098722023 @default.
- W2076609872 crossrefType "journal-article" @default.
- W2076609872 hasAuthorship W2076609872A5006690579 @default.
- W2076609872 hasAuthorship W2076609872A5010100874 @default.
- W2076609872 hasAuthorship W2076609872A5016211526 @default.
- W2076609872 hasAuthorship W2076609872A5017480661 @default.
- W2076609872 hasAuthorship W2076609872A5020137042 @default.
- W2076609872 hasAuthorship W2076609872A5025486151 @default.
- W2076609872 hasAuthorship W2076609872A5032886347 @default.
- W2076609872 hasAuthorship W2076609872A5034594283 @default.
- W2076609872 hasAuthorship W2076609872A5052313487 @default.
- W2076609872 hasAuthorship W2076609872A5055963262 @default.
- W2076609872 hasAuthorship W2076609872A5063928870 @default.
- W2076609872 hasAuthorship W2076609872A5077822196 @default.
- W2076609872 hasBestOaLocation W20766098721 @default.
- W2076609872 hasConcept C118487528 @default.
- W2076609872 hasConcept C126322002 @default.
- W2076609872 hasConcept C134018914 @default.