Literature DB >> 19800004

Kalirin loss results in cortical morphological alterations.

Zhong Xie1, Michael E Cahill, Peter Penzes.   

Abstract

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. Copyright 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 19800004      PMCID: PMC2818244          DOI: 10.1016/j.mcn.2009.09.006

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  56 in total

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6.  Reduced dendritic spine density on cerebral cortical pyramidal neurons in schizophrenia.

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Journal:  J Neurosci       Date:  2008-11-19       Impact factor: 6.167

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Authors:  Zhong Xie; Huzefa Photowala; Michael E Cahill; Deepak P Srivastava; Kevin M Woolfrey; Cassandra Y Shum; Richard L Huganir; Peter Penzes
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  31 in total

Review 1.  Glutamatergic postsynaptic density protein dysfunctions in synaptic plasticity and dendritic spines morphology: relevance to schizophrenia and other behavioral disorders pathophysiology, and implications for novel therapeutic approaches.

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3.  Kalirin-7 prevents dendritic spine dysgenesis induced by amyloid beta-derived oligomers.

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Review 4.  Developmental vulnerability of synapses and circuits associated with neuropsychiatric disorders.

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Review 6.  Dendritic spine pathology in neuropsychiatric disorders.

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Review 7.  KALRN: A central regulator of synaptic function and synaptopathies.

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8.  Age-dependent increase in Kalirin-9 and Kalirin-12 transcripts in human orbitofrontal cortex.

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9.  Mammalian diseases of phosphatidylinositol transfer proteins and their homologs.

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10.  Neuregulin1 signaling promotes dendritic spine growth through kalirin.

Authors:  Michael E Cahill; Christine Remmers; Kelly A Jones; Zhong Xie; Robert A Sweet; Peter Penzes
Journal:  J Neurochem       Date:  2013-06-27       Impact factor: 5.372

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