TY - JOUR
T1 - CRP1, a protein localized in filopodia of growth cones, is involved in dendritic growth
AU - Ma, Liping
AU - Greenwood, Jeffrey A.
AU - Schachner, Melitta
PY - 2011/11/16
Y1 - 2011/11/16
N2 - The cysteine-rich protein (CRP) family is a subgroup of LIM domain proteins. CRP1, which cross-links actin filaments to make actin bundles, is the onlyCRPfamily member expressed in the CNS with little known about its function in nerve cells. Here, we report that CRP1 colocalizes with actin in the filopodia of growth cones in cultured rat hippocampal neurons. Knockdown of CRP1 expression by short hairpinRNAinterference results in inhibition of filopodia formation and dendritic growth in neurons. Overexpression of CRP1 increases filopodia formation and neurite branching, which require its actin-bundling activity. Expression ofCRP1with a constitutively active form of Cdc42, a GTPase involved in filopodia formation, increases filopodia formation in COS-7 cells, suggesting cooperation between the two proteins. Moreover, we demonstrate that neuronal activity upregulates CRP1 expression in hippocampal neurons via Ca 2+ influx after depolarization. Ca 2+/calmodulin-dependent protein kinase IV (CaMKIV) and cAMP response element binding protein mediate the Ca 2+-induced upregulation of CRP1 expression. Furthermore, CRP1 is required for the dendritic growth induced by Ca 2+ influx or CaMKIV. Together, these data are the first to demonstrate a role for CRP1 in dendritic growth.
AB - The cysteine-rich protein (CRP) family is a subgroup of LIM domain proteins. CRP1, which cross-links actin filaments to make actin bundles, is the onlyCRPfamily member expressed in the CNS with little known about its function in nerve cells. Here, we report that CRP1 colocalizes with actin in the filopodia of growth cones in cultured rat hippocampal neurons. Knockdown of CRP1 expression by short hairpinRNAinterference results in inhibition of filopodia formation and dendritic growth in neurons. Overexpression of CRP1 increases filopodia formation and neurite branching, which require its actin-bundling activity. Expression ofCRP1with a constitutively active form of Cdc42, a GTPase involved in filopodia formation, increases filopodia formation in COS-7 cells, suggesting cooperation between the two proteins. Moreover, we demonstrate that neuronal activity upregulates CRP1 expression in hippocampal neurons via Ca 2+ influx after depolarization. Ca 2+/calmodulin-dependent protein kinase IV (CaMKIV) and cAMP response element binding protein mediate the Ca 2+-induced upregulation of CRP1 expression. Furthermore, CRP1 is required for the dendritic growth induced by Ca 2+ influx or CaMKIV. Together, these data are the first to demonstrate a role for CRP1 in dendritic growth.
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U2 - 10.1523/JNEUROSCI.2595-11.2011
DO - 10.1523/JNEUROSCI.2595-11.2011
M3 - Article
C2 - 22090504
AN - SCOPUS:81255195528
SN - 0270-6474
VL - 31
SP - 16781
EP - 16791
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 46
ER -