1998
DOI: 10.1016/s0006-8993(98)00498-3
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Affinity-purification and characterization of caveolins from the brain: Differential expression of caveolin-1, -2, and -3 in brain endothelial and astroglial cell types

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Cited by 179 publications
(173 citation statements)
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“…Indeed, caveolar-like microdomains (CLMs) were termed as the neuronal counterpart to non-neuronal caveolae. More recently, however, various reports have demonstrated the expression off all three caveolin isoforms in neurons [29,30,[83][84][85][86]. Data described below is consistent with reports from non-neuronal tissue and the initial descriptions in Dominique Toran-Allerand's review that caveolin proteins play an essential role in brain membrane estrogen receptor function.…”
Section: Caveolin Proteins and Estrogen Receptorssupporting
confidence: 87%
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“…Indeed, caveolar-like microdomains (CLMs) were termed as the neuronal counterpart to non-neuronal caveolae. More recently, however, various reports have demonstrated the expression off all three caveolin isoforms in neurons [29,30,[83][84][85][86]. Data described below is consistent with reports from non-neuronal tissue and the initial descriptions in Dominique Toran-Allerand's review that caveolin proteins play an essential role in brain membrane estrogen receptor function.…”
Section: Caveolin Proteins and Estrogen Receptorssupporting
confidence: 87%
“…There are three known caveolin proteins, caveolin 1 (CAV1, with splice variants α and β), caveolin 2 (CAV2), and caveolin 3 (CAV3) [26][27][28]. CAV1 and CAV2 have overlapping expression patterns in a variety of cell types including, neurons and glia [29,30], endothelial [31], and epithelial cells [32]. Disruption of CAV2 expression does not affect caveolae formation in vivo [33], inasmuch it is hypothesized that CAV2 only forms caveolae as hetero-oligomers with CAV1, and not in isolation [34].…”
Section: Caveolins: Important For the Trafficking And Clustering Of Mmentioning
confidence: 99%
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“…Caveolae are low density membrane microdomains that have been implicated in initiating the signaling events induced by growth factors, such as epidermal growth factor and endothelin-1, and receptors for these ligands are enriched within caveolae. 17 As expected, caveolin-1, a characteristic caveolar marker protein in the brain, 18 appeared to be retained in the Triton X-100 -insoluble fraction under basal conditions and after ICAM-1 crosslinking ( Figure 5D). Under basal ( Figure 5A) and ICAM-1 cross-linking conditions (data not shown), ICAM-1 and caveolin-1 showed no significant colocalization in GP8/3.9 cells, although data from sucrose density gradient fractionation of GP8/3.9 cell lysates showed that caveolin-1 and ICAM-1 cofractionated ( Figure 5C).…”
Section: Icam-1 and Caveolin-1 Cofractionate On Sucrose Density Gradisupporting
confidence: 74%
“…In brain, caveolins 1, 2 and 3 are expressed. Caveolin 3 was predominantly found on the endfeet of astrocytic processes, but not on neurons (Ikezu et al, 1998a). Dystroglycan is also present at astrocytic endfeet (Guadagno and Moukhles, 2004b).…”
Section: Caveolin-3mentioning
confidence: 92%