Plasma and intracellular membrane inositol 1,4,5-trisphosphate receptors mediate the Ca<SUP>2+</SUP> increase associated with the ATP-induced increase in ciliary beat frequency
dc.contributor.author | Barrera, NP | |
dc.contributor.author | Morales, B | |
dc.contributor.author | Villalón, M | |
dc.date.accessioned | 2025-01-21T01:07:36Z | |
dc.date.available | 2025-01-21T01:07:36Z | |
dc.date.issued | 2004 | |
dc.description.abstract | An increase in intracellular free Ca2+ concentration ([Ca2+](i)) has been shown to be involved in the increase in ciliary beat frequency (CBF) in response to ATP; however, the signaling pathways associated with inositol 1,4,5-trisphosphate (IP3) receptor-dependent Ca2+ mobilization remain unresolved. Using radioimmunoassay techniques, we have demonstrated the appearance of two IP3 peaks occurring 10 and 60 s after ATP addition, which was strongly correlated with a release of intracellular Ca2+ from internal stores and an influx of extracellular Ca2+, respectively. In addition, ATP-dependent Ca2+ mobilization required protein kinase C (PKC) and Ca2+/ calmodulin-dependent protein kinase II activation. We found an increase in PKC activity in response to ATP, with a peak at 60 s after ATP addition. Xestospongin C, an IP3 receptor blocker, significantly diminished both the ATP-induced increase in CBF and the initial transient [Ca2+](i) component. ATP addition in the presence of xestospongin C or thapsigargin revealed that the Ca2+ influx is also dependent on IP3 receptor activation. Immunofluorescence and confocal microscopic studies showed the presence of IP3 receptor types 1 and 3 in cultured ciliated cells. Immunogold electron microscopy localized IP3 receptor type 3 to the nucleus, the endoplasmic reticulum, and, interestingly, the plasma membrane. In contrast, IP3 receptor type 1 was found exclusively in the nucleus and the endoplasmic reticulum. Our study demonstrates for the first time the presence of IP3 receptor type 3 in the plasma membrane in ciliated cells and leads us to postulate that the IP3 receptor can directly trigger Ca2+ influx in response to ATP. | |
dc.fuente.origen | WOS | |
dc.identifier.doi | 10.1152/ajpcell.00343.2003 | |
dc.identifier.eissn | 1522-1563 | |
dc.identifier.issn | 0363-6143 | |
dc.identifier.uri | https://doi.org/10.1152/ajpcell.00343.2003 | |
dc.identifier.uri | https://repositorio.uc.cl/handle/11534/96355 | |
dc.identifier.wosid | WOS:000223762000032 | |
dc.issue.numero | 4 | |
dc.language.iso | en | |
dc.pagina.final | C1124 | |
dc.pagina.inicio | C1114 | |
dc.revista | American journal of physiology-cell physiology | |
dc.rights | acceso restringido | |
dc.subject | transduction mechanisms | |
dc.subject | P2Y receptor | |
dc.subject | calcium influx | |
dc.subject.ods | 03 Good Health and Well-being | |
dc.subject.odspa | 03 Salud y bienestar | |
dc.title | Plasma and intracellular membrane inositol 1,4,5-trisphosphate receptors mediate the Ca<SUP>2+</SUP> increase associated with the ATP-induced increase in ciliary beat frequency | |
dc.type | artículo | |
dc.volumen | 287 | |
sipa.index | WOS | |
sipa.trazabilidad | WOS;2025-01-12 |