Matches in SemOpenAlex for { <https://semopenalex.org/work/W2018680437> ?p ?o ?g. }
- W2018680437 endingPage "321" @default.
- W2018680437 startingPage "313" @default.
- W2018680437 abstract "Glomerular podocytes play a key role in maintaining the integrity of the glomerular filtration barrier. This function may be regulated by angiotensin II (Ang II) through activation of cell-surface receptors. Although studies suggest that podocytes express receptors for Ang II, the Ang II binding site has not been characterized with radioligand binding techniques. We therefore used iodine 125-labeled Ang II to monitor Ang II-receptor density during differentiation of a mouse podocyte cell line. Scatchard analyses of equilibrium binding data revealed a single class of high-affinity binding sites (dissociation constant approximately 3 nmol/L) in both differentiated and nondifferentiated cells. During differentiation, the density of Ang II-receptor sites increased roughly 15-fold in differentiated podocytes (maximal density of specific binding sites 881 fmol/mg protein) compared with that in nondifferentiated cells (52 fmol/mg protein; P<.005). Glomerular podocytes expressed messenger RNA for AT1A, AT1B, and AT2 receptor subtypes, and competitive binding studies found that differentiated podocytes expressed mostly AT1 receptors (approximately 75%) with lesser amounts of AT2 (approximately 25%). Up-regulation of Ang II-receptor number was associated with increased Ang II-receptor responsiveness, as evidenced by enhanced Ang II-stimulated inositol phosphate (IP) generation and incorporation of tritiated thymidine. Both [3H]thymidine incorporation and IP generation were mediated by AT1-receptor activation. These data suggest that glomerular podocytes express a high-affinity binding site for Ang II with pharmacologic characteristics of both AT1 and AT2 receptors. This receptor site is up-regulated during podocyte differentiation, and receptor activation induces both IP generation and DNA synthesis by AT1-dependent mechanisms. We speculate that activation of podocyte Ang II receptors contributes to glomerular damage in disease states." @default.
- W2018680437 created "2016-06-24" @default.
- W2018680437 creator A5007293606 @default.
- W2018680437 creator A5022045066 @default.
- W2018680437 creator A5045282174 @default.
- W2018680437 date "2003-11-01" @default.
- W2018680437 modified "2023-09-23" @default.
- W2018680437 title "Characterization of angiotensin II–receptor subtypes in podocytes" @default.
- W2018680437 cites W1527240164 @default.
- W2018680437 cites W1591510379 @default.
- W2018680437 cites W1965570459 @default.
- W2018680437 cites W1967561584 @default.
- W2018680437 cites W1968874083 @default.
- W2018680437 cites W1971498397 @default.
- W2018680437 cites W1981308965 @default.
- W2018680437 cites W1983649348 @default.
- W2018680437 cites W1984775628 @default.
- W2018680437 cites W1992425802 @default.
- W2018680437 cites W2000938726 @default.
- W2018680437 cites W2002237956 @default.
- W2018680437 cites W2004295184 @default.
- W2018680437 cites W2006592008 @default.
- W2018680437 cites W2010031713 @default.
- W2018680437 cites W2013690237 @default.
- W2018680437 cites W2017800047 @default.
- W2018680437 cites W2025458195 @default.
- W2018680437 cites W2037154107 @default.
- W2018680437 cites W2039063169 @default.
- W2018680437 cites W2052352814 @default.
- W2018680437 cites W2054225562 @default.
- W2018680437 cites W2068838843 @default.
- W2018680437 cites W2074998975 @default.
- W2018680437 cites W2083455540 @default.
- W2018680437 cites W2086389958 @default.
- W2018680437 cites W2110230080 @default.
- W2018680437 cites W2114938192 @default.
- W2018680437 cites W2117044603 @default.
- W2018680437 cites W2119534102 @default.
- W2018680437 cites W2119995804 @default.
- W2018680437 cites W2129416468 @default.
- W2018680437 cites W2131033837 @default.
- W2018680437 cites W2133485626 @default.
- W2018680437 cites W2134319114 @default.
- W2018680437 cites W2155522776 @default.
- W2018680437 cites W2169665073 @default.
- W2018680437 cites W2171001136 @default.
- W2018680437 cites W2275083029 @default.
- W2018680437 cites W2281691222 @default.
- W2018680437 cites W4293247451 @default.
- W2018680437 cites W4317524290 @default.
- W2018680437 doi "https://doi.org/10.1016/s0022-2143(03)00139-2" @default.
- W2018680437 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/14647035" @default.
- W2018680437 hasPublicationYear "2003" @default.
- W2018680437 type Work @default.
- W2018680437 sameAs 2018680437 @default.
- W2018680437 citedByCount "37" @default.
- W2018680437 countsByYear W20186804372012 @default.
- W2018680437 countsByYear W20186804372013 @default.
- W2018680437 countsByYear W20186804372015 @default.
- W2018680437 countsByYear W20186804372018 @default.
- W2018680437 countsByYear W20186804372019 @default.
- W2018680437 countsByYear W20186804372021 @default.
- W2018680437 crossrefType "journal-article" @default.
- W2018680437 hasAuthorship W2018680437A5007293606 @default.
- W2018680437 hasAuthorship W2018680437A5022045066 @default.
- W2018680437 hasAuthorship W2018680437A5045282174 @default.
- W2018680437 hasConcept C104849204 @default.
- W2018680437 hasConcept C107824862 @default.
- W2018680437 hasConcept C123915805 @default.
- W2018680437 hasConcept C126322002 @default.
- W2018680437 hasConcept C134018914 @default.
- W2018680437 hasConcept C153911025 @default.
- W2018680437 hasConcept C170493617 @default.
- W2018680437 hasConcept C185592680 @default.
- W2018680437 hasConcept C2777146197 @default.
- W2018680437 hasConcept C2779561371 @default.
- W2018680437 hasConcept C2780091579 @default.
- W2018680437 hasConcept C2780368995 @default.
- W2018680437 hasConcept C2908929049 @default.
- W2018680437 hasConcept C3018920779 @default.
- W2018680437 hasConcept C55493867 @default.
- W2018680437 hasConcept C67847695 @default.
- W2018680437 hasConcept C71924100 @default.
- W2018680437 hasConcept C86803240 @default.
- W2018680437 hasConcept C95444343 @default.
- W2018680437 hasConceptScore W2018680437C104849204 @default.
- W2018680437 hasConceptScore W2018680437C107824862 @default.
- W2018680437 hasConceptScore W2018680437C123915805 @default.
- W2018680437 hasConceptScore W2018680437C126322002 @default.
- W2018680437 hasConceptScore W2018680437C134018914 @default.
- W2018680437 hasConceptScore W2018680437C153911025 @default.
- W2018680437 hasConceptScore W2018680437C170493617 @default.
- W2018680437 hasConceptScore W2018680437C185592680 @default.
- W2018680437 hasConceptScore W2018680437C2777146197 @default.
- W2018680437 hasConceptScore W2018680437C2779561371 @default.
- W2018680437 hasConceptScore W2018680437C2780091579 @default.
- W2018680437 hasConceptScore W2018680437C2780368995 @default.
- W2018680437 hasConceptScore W2018680437C2908929049 @default.