MSK1 regulates homeostatic and experience-dependent synaptic plasticity. / Corrêa, Sonia A. L. ; Hunter, Christopher J.; Palygin, Oleg; Wauters, S.C.; Martin, Kirsty J.; McKenzie, Colin; McKelvey, Kim; Morris, Richard G. M. ; Pankratov, Yuriy; Arthur, J.Simon C.; Frenguelli, BrunoG.
In: Journal of Neuroscience, Vol. 32, No. 38, 2012, p. 13039-13051.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - MSK1 regulates homeostatic and experience-dependent synaptic plasticity
A1 - Corrêa,Sonia A. L.
A1 - Hunter,Christopher J.
A1 - Palygin,Oleg
A1 - Wauters,S.C.
A1 - Martin,Kirsty J.
A1 - McKenzie,Colin
A1 - McKelvey,Kim
A1 - Morris,Richard G. M.
A1 - Pankratov,Yuriy
A1 - Arthur,J.Simon C.
A1 - Frenguelli,BrunoG.
AU - Corrêa,Sonia A. L.
AU - Hunter,Christopher J.
AU - Palygin,Oleg
AU - Wauters,S.C.
AU - Martin,Kirsty J.
AU - McKenzie,Colin
AU - McKelvey,Kim
AU - Morris,Richard G. M.
AU - Pankratov,Yuriy
AU - Arthur,J.Simon C.
AU - Frenguelli,BrunoG.
PY - 2012
Y1 - 2012
N2 - The ability of neurons to modulate synaptic strength underpins synaptic plasticity, learning and memory, and adaptation to sensory experience. Despite the importance of synaptic adaptation in directing, reinforcing, and revising the behavioral response to environmental influences, the cellular and molecular mechanisms underlying synaptic adaptation are far from clear. Brain-derived neurotrophic factor (BDNF) is a prime initiator of structural and functional synaptic adaptation. However, the signaling cascade activated by BDNF to initiate these adaptive changes has not been elucidated. We have previously shown that BDNF activates mitogen- and stress-activated kinase 1 (MSK1), which regulates gene transcription via the phosphorylation of both CREB and histone H3. Using mice with a kinase-dead knock-in mutation of MSK1, we now show that MSK1 is necessary for the upregulation of synaptic strength in response to environmental enrichment in vivo. Furthermore, neurons from MSK1 kinase-dead mice failed to show scaling of synaptic transmission in response to activity deprivation in vitro, a deficit that could be rescued by reintroduction of wild-type MSK1. We also show that MSK1 forms part of a BDNF-and MAPK-dependent signaling cascade required for homeostatic synaptic scaling, which likely resides in the ability of MSK1 to regulate cell surface GluA1 expression via the induction of Arc/Arg3.1. These results demonstrate that MSK1 is an integral part of a signaling pathway that underlies the adaptive response to synaptic and environmental experience. MSK1 may thus act as a key homeostat in the activity- and experience-dependent regulation of synaptic strength. © 2012 the authors.
AB - The ability of neurons to modulate synaptic strength underpins synaptic plasticity, learning and memory, and adaptation to sensory experience. Despite the importance of synaptic adaptation in directing, reinforcing, and revising the behavioral response to environmental influences, the cellular and molecular mechanisms underlying synaptic adaptation are far from clear. Brain-derived neurotrophic factor (BDNF) is a prime initiator of structural and functional synaptic adaptation. However, the signaling cascade activated by BDNF to initiate these adaptive changes has not been elucidated. We have previously shown that BDNF activates mitogen- and stress-activated kinase 1 (MSK1), which regulates gene transcription via the phosphorylation of both CREB and histone H3. Using mice with a kinase-dead knock-in mutation of MSK1, we now show that MSK1 is necessary for the upregulation of synaptic strength in response to environmental enrichment in vivo. Furthermore, neurons from MSK1 kinase-dead mice failed to show scaling of synaptic transmission in response to activity deprivation in vitro, a deficit that could be rescued by reintroduction of wild-type MSK1. We also show that MSK1 forms part of a BDNF-and MAPK-dependent signaling cascade required for homeostatic synaptic scaling, which likely resides in the ability of MSK1 to regulate cell surface GluA1 expression via the induction of Arc/Arg3.1. These results demonstrate that MSK1 is an integral part of a signaling pathway that underlies the adaptive response to synaptic and environmental experience. MSK1 may thus act as a key homeostat in the activity- and experience-dependent regulation of synaptic strength. © 2012 the authors.
U2 - 10.1523/JNEUROSCI.0930-12.2012
DO - 10.1523/JNEUROSCI.0930-12.2012
M1 - Article
JO - Journal of Neuroscience
JF - Journal of Neuroscience
SN - 0270-6474
IS - 38
VL - 32
SP - 13039
EP - 13051
ER -