Abstract
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Current Biology |
| Vol/bind | 15 |
| Udgave nummer | 20 |
| Sider (fra-til) | 1861-1866 |
| ISSN | 0960-9822 |
| DOI | |
| Status | Udgivet - 2005 |
Adgang til dokumentet
Citationsformater
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS
PDGFRaa Signaling Is Regulated through the Primary Cilium in Fibroblasts. / Schneider, Linda; Clement, Christian Alexandro; Teilmann, S.C.; Pazour, G.; Hofman, Kay; Satir, P.; Christensen, Søren T.
I: Current Biology, Bind 15, Nr. 20, 2005, s. 1861-1866.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - PDGFRaa Signaling Is Regulated through the Primary Cilium in Fibroblasts
AU - Schneider, Linda
AU - Clement, Christian Alexandro
AU - Teilmann, S.C.
AU - Pazour, G.
AU - Hofman, Kay
AU - Satir, P.
AU - Christensen, Søren T.
PY - 2005
Y1 - 2005
N2 - Recent findings show that cilia are sensory organelles that display specific receptors and ion channels, which transmit signals from the extracellular environment via the cilium to the cell to control tissue homeostasis and function [[1], [2], [3], [4], [5] and [6]]. Agenesis of primary cilia or mislocation of ciliary signal components affects human pathologies, such as polycystic kidney disease [7] and disorders associated with Bardet-Biedl syndrome [8]. Primary cilia are essential for hedgehog ligand-induced signaling cascade regulating growth and patterning [[9] and [10]]. Here, we show that the primary cilium in fibroblasts [11] plays a critical role in growth control via platelet-derived growth factor receptor a (PDGFRa), which localizes to the primary cilium during growth arrest in NIH3T3 cells and primary cultures of mouse embryonic fibroblasts. Ligand-dependent activation of PDGFRaa is followed by activation of Akt and the Mek1/2-Erk1/2 pathways, with Mek1/2 being phosphorylated within the cilium and at the basal body. Fibroblasts derived from Tg737orpk mutants fail to form normal cilia and to upregulate the level of PDGFRa; PDGF-AA fails to activate PDGFRaa and the Mek1/2-Erk1/2 pathway. Signaling through PDGFRß, which localizes to the plasma membrane, is maintained at comparable levels in wild-type and mutant cells. We propose that ciliary PDGFRaa signaling is linked to tissue homeostasis and to mitogenic signaling pathways.
AB - Recent findings show that cilia are sensory organelles that display specific receptors and ion channels, which transmit signals from the extracellular environment via the cilium to the cell to control tissue homeostasis and function [[1], [2], [3], [4], [5] and [6]]. Agenesis of primary cilia or mislocation of ciliary signal components affects human pathologies, such as polycystic kidney disease [7] and disorders associated with Bardet-Biedl syndrome [8]. Primary cilia are essential for hedgehog ligand-induced signaling cascade regulating growth and patterning [[9] and [10]]. Here, we show that the primary cilium in fibroblasts [11] plays a critical role in growth control via platelet-derived growth factor receptor a (PDGFRa), which localizes to the primary cilium during growth arrest in NIH3T3 cells and primary cultures of mouse embryonic fibroblasts. Ligand-dependent activation of PDGFRaa is followed by activation of Akt and the Mek1/2-Erk1/2 pathways, with Mek1/2 being phosphorylated within the cilium and at the basal body. Fibroblasts derived from Tg737orpk mutants fail to form normal cilia and to upregulate the level of PDGFRa; PDGF-AA fails to activate PDGFRaa and the Mek1/2-Erk1/2 pathway. Signaling through PDGFRß, which localizes to the plasma membrane, is maintained at comparable levels in wild-type and mutant cells. We propose that ciliary PDGFRaa signaling is linked to tissue homeostasis and to mitogenic signaling pathways.
U2 - 10.1016/j.cub.2005.09.012
DO - 10.1016/j.cub.2005.09.012
M3 - Journal article
VL - 15
SP - 1861
EP - 1866
JO - Current Biology
JF - Current Biology
SN - 0960-9822
IS - 20
ER -