Matches in SemOpenAlex for { <https://semopenalex.org/work/W3138839669> ?p ?o ?g. }
- W3138839669 endingPage "1832" @default.
- W3138839669 startingPage "1816" @default.
- W3138839669 abstract "Fragile X syndrome (FXS) is the leading monogenic cause of intellectual disability and autism spectrum disorders. With increasing investigation into the molecular mechanisms underlying FXS, there is growing evidence that perturbations in glial signaling are widely associated with neurological pathology. Purinergic signaling, which utilizes nucleoside triphosphates as signaling molecules, provides one of the most ubiquitous signaling systems for glial-neuronal and glial-glial crosstalk. Here, we sought to identify whether purinergic signaling is dysregulated within the FXS mouse cortex, and whether this dysregulation contributes to aberrant intercellular communication. In primary astrocyte cultures derived from the Fmr1 knockout (KO) mouse model of FXS, we found that application of exogenous ATP and UTP evoked elevated intracellular calcium responses compared to wildtype levels. Accordingly, purinergic P2Y2 and P2Y6 receptor expression was increased in Fmr1 KO astrocytes both in vitro and in acutely dissociated tissue, while P2Y antagonism via suramin prevented intracellular calcium elevations, suggesting a role for these receptors in aberrant FXS astrocyte activation. To investigate the impact of elevated purinergic signaling on astrocyte-mediated synaptogenesis, we quantified synaptogenic protein TSP-1, known to be regulated by P2Y activation. TSP-1 secretion and expression were both heightened in Fmr1 KO vs wildtype astrocytes following UTP application, while naïve TSP-1 cortical expression was also transiently elevated in vivo, indicating increased potential for excitatory TSP-1-mediated synaptogenesis in the FXS cortex. Together, our results demonstrate novel and significant purinergic signaling elevations in Fmr1 KO astrocytes, which may serve as a potential therapeutic target to mitigate the signaling aberrations observed in FXS." @default.
- W3138839669 created "2021-03-29" @default.
- W3138839669 creator A5024005856 @default.
- W3138839669 creator A5049109562 @default.
- W3138839669 creator A5088213319 @default.
- W3138839669 date "2021-03-22" @default.
- W3138839669 modified "2023-10-02" @default.
- W3138839669 title "Astrocyte‐mediated purinergic signaling is upregulated in a mouse model of Fragile X syndrome" @default.
- W3138839669 cites W1528423284 @default.
- W3138839669 cites W1535975452 @default.
- W3138839669 cites W1611735695 @default.
- W3138839669 cites W1794950817 @default.
- W3138839669 cites W1833314573 @default.
- W3138839669 cites W1875583344 @default.
- W3138839669 cites W1965484171 @default.
- W3138839669 cites W1982934241 @default.
- W3138839669 cites W1984618862 @default.
- W3138839669 cites W1988452935 @default.
- W3138839669 cites W1992826480 @default.
- W3138839669 cites W1994905856 @default.
- W3138839669 cites W1995530514 @default.
- W3138839669 cites W1995671386 @default.
- W3138839669 cites W2002780348 @default.
- W3138839669 cites W2002903762 @default.
- W3138839669 cites W2013419706 @default.
- W3138839669 cites W2014255722 @default.
- W3138839669 cites W2017750240 @default.
- W3138839669 cites W2022421090 @default.
- W3138839669 cites W2026147918 @default.
- W3138839669 cites W2027917639 @default.
- W3138839669 cites W2050429474 @default.
- W3138839669 cites W2050692236 @default.
- W3138839669 cites W2056358535 @default.
- W3138839669 cites W2058797642 @default.
- W3138839669 cites W2066073800 @default.
- W3138839669 cites W2069011094 @default.
- W3138839669 cites W2071482305 @default.
- W3138839669 cites W2087009012 @default.
- W3138839669 cites W2087311190 @default.
- W3138839669 cites W2089686007 @default.
- W3138839669 cites W2092742762 @default.
- W3138839669 cites W2093498373 @default.
- W3138839669 cites W2095138676 @default.
- W3138839669 cites W2097135760 @default.
- W3138839669 cites W2098622411 @default.
- W3138839669 cites W2129896275 @default.
- W3138839669 cites W2137395087 @default.
- W3138839669 cites W2141260882 @default.
- W3138839669 cites W2143882188 @default.
- W3138839669 cites W2147140183 @default.
- W3138839669 cites W2149579087 @default.
- W3138839669 cites W2153646819 @default.
- W3138839669 cites W2153955573 @default.
- W3138839669 cites W2155465918 @default.
- W3138839669 cites W2158972964 @default.
- W3138839669 cites W2160777380 @default.
- W3138839669 cites W2166941550 @default.
- W3138839669 cites W2236139809 @default.
- W3138839669 cites W2277998802 @default.
- W3138839669 cites W2321319950 @default.
- W3138839669 cites W2325591484 @default.
- W3138839669 cites W2327536542 @default.
- W3138839669 cites W2411374129 @default.
- W3138839669 cites W2469266539 @default.
- W3138839669 cites W2474147716 @default.
- W3138839669 cites W2476729051 @default.
- W3138839669 cites W2479769265 @default.
- W3138839669 cites W2518688015 @default.
- W3138839669 cites W2575460261 @default.
- W3138839669 cites W2587833244 @default.
- W3138839669 cites W2616987016 @default.
- W3138839669 cites W2736612025 @default.
- W3138839669 cites W2745685952 @default.
- W3138839669 cites W2752011313 @default.
- W3138839669 cites W2769140026 @default.
- W3138839669 cites W2790931908 @default.
- W3138839669 cites W2796199026 @default.
- W3138839669 cites W2802424922 @default.
- W3138839669 cites W2884522219 @default.
- W3138839669 cites W2886733693 @default.
- W3138839669 cites W2889500216 @default.
- W3138839669 cites W2894425411 @default.
- W3138839669 cites W2953275777 @default.
- W3138839669 doi "https://doi.org/10.1002/glia.23997" @default.
- W3138839669 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/33754385" @default.
- W3138839669 hasPublicationYear "2021" @default.
- W3138839669 type Work @default.
- W3138839669 sameAs 3138839669 @default.
- W3138839669 citedByCount "10" @default.
- W3138839669 countsByYear W31388396692021 @default.
- W3138839669 countsByYear W31388396692022 @default.
- W3138839669 countsByYear W31388396692023 @default.
- W3138839669 crossrefType "journal-article" @default.
- W3138839669 hasAuthorship W3138839669A5024005856 @default.
- W3138839669 hasAuthorship W3138839669A5049109562 @default.
- W3138839669 hasAuthorship W3138839669A5088213319 @default.
- W3138839669 hasConcept C104317684 @default.
- W3138839669 hasConcept C160225129 @default.