4.3 Article

Kalirin loss results in cortical morphological alterations

Journal

MOLECULAR AND CELLULAR NEUROSCIENCE
Volume 43, Issue 1, Pages 81-89

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.mcn.2009.09.006

Keywords

Dendrites; Synaptic plasticity; Prefrontal cortex; Rac1; Knockout; KALRN; Small GTPase; Dendritic spine

Categories

Funding

  1. NIH-NIMH [R01MH071316]
  2. National Alliance for Autism Research (NAAR)
  3. National Alliance for Research on Schizophrenia and Depression (NARSAD)
  4. Alzheimer's Association
  5. NINDS [5T32NS041234-08]
  6. NIH [1F31AG031621-01A2]
  7. NATIONAL INSTITUTE OF MENTAL HEALTH [R01MH071316] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [T32NS041234] Funding Source: NIH RePORTER
  9. NATIONAL INSTITUTE ON AGING [F31AG031621] Funding Source: NIH RePORTER

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Morphogenesis of pyramidal neuronal dendrites and spines is Crucial for the formation and refinement of forebrain neuronal Circuits underlying cognition. Aberrant dendrite and spine morphology is associated with neuropathological disorders. However, the molecular mechanisms controlling pyramidal neuronal dendrite and spine morphogenesis in vivo remain largely unknown. Kalirin is a brain-specific guanine-nucleotide exchange factor for Rho-like small GTPases, and an important regulator of spine morphogenesis in cultured neurons. Here we show that RNAi-dependent knockdown of kalirin in cultured neurons affected dendrite morphology. Cortical pyramidal neurons from KALRN-null mice showed reduced spine density and impaired activity-dependent spine plasticity; and they exhibited reduced complexity of dendritic trees. KALRN-null mice also displayed smaller neuronal cell bodies and reductions in the size of the cortex and cortical layers. These data demonstrate important roles for kalirin in the regulation of cortical Structure, ultrastructure, and spine Structural plasticity. (C) 2009 Elsevier Inc. All rights reserved.

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