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The Journal of Neuroscience, March 12, 2008, 28(11):2903-2911; doi:10.1523/JNEUROSCI.0225-08.2008

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Development/Plasticity/Repair
Rapid Loss of Dendritic Spines after Stress Involves Derangement of Spine Dynamics by Corticotropin-Releasing Hormone

Yuncai Chen,¹ Céline M. Dubé,¹ Courtney J. Rice,² and Tallie Z. Baram^1,2

Departments of ¹Pediatrics and ²Anatomy/Neurobiology, University of California Irvine, Irvine, California 92697-4475

Correspondence should be addressed to Dr. Tallie Z. Baram, Departments of Pediatrics and Anatomy/Neurobiology, University of California Irvine, Medical Sciences I, ZOT: 4475, Irvine, CA 92697-4475. Email: tallie{at}uci.edu

Chronic stress causes dendritic regression and loss of dendritic spines in hippocampal neurons that is accompanied by deficits in synaptic plasticity and memory. However, the responsible mechanisms remain unresolved. Here, we found that within hours of the onset of stress, the density of dendritic spines declined in vulnerable dendritic domains. This rapid, stress-induced spine loss was abolished by blocking the receptor (CRFR₁) of corticotropin-releasing hormone (CRH), a hippocampal neuropeptide released during stress. Exposure to CRH provoked spine loss and dendritic regression in hippocampal organotypic cultures, and selective blockade of the CRFR₁ receptor had the opposite effect. Live, time-lapse imaging revealed that CRH reduced spine density by altering dendritic spine dynamics: the peptide selectively and reversibly accelerated spine retraction, and this mechanism involved destabilization of spine F-actin. In addition, mice lacking the CRFR₁ receptor had augmented spine density. These findings support a mechanistic role for CRH–CRFR₁ signaling in stress-evoked spine loss and dendritic remodeling.

Key words: dendritic spine; stress; CRF; CRH; actin; synaptic plasticity; two photon; hippocampus

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Received Nov. 21, 2007; accepted Feb. 4, 2008.

Correspondence should be addressed to Dr. Tallie Z. Baram, Departments of Pediatrics and Anatomy/Neurobiology, University of California Irvine, Medical Sciences I, ZOT: 4475, Irvine, CA 92697-4475. Email: tallie{at}uci.edu

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				H. Sugiura, H. Tanaka, S. Yasuda, T. Takemiya, and K. Yamagata Transducing Neuronal Activity into Dendritic Spine Morphology: New Roles for p38 MAP Kinase and N-cadherin Neuroscientist, February 1, 2009; 15(1): 90 - 104. [Abstract] [PDF]

				H. Sheng, T. Sun, B. Cong, P. He, Y. Zhang, J. Yan, C. Lu, and X. Ni Corticotropin-releasing hormone stimulates SGK-1 kinase expression in cultured hippocampal neurons via CRH-R1 Am J Physiol Endocrinol Metab, October 1, 2008; 295(4): E938 - E946. [Abstract] [Full Text] [PDF]

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