Literature DB >> 19217433

Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations.

Jennifer L Larimore1, Christopher A Chapleau, Shinichi Kudo, Anne Theibert, Alan K Percy, Lucas Pozzo-Miller.   

Abstract

The expression of the methylated DNA-binding protein MeCP2 increases during neuronal development, which suggests that this epigenetic factor is crucial for neuronal terminal differentiation. We evaluated dendritic and axonal development in embryonic day-18 hippocampal neurons in culture by measuring total length and counting branch point numbers at 4 days in vitro, well before synapse formation. Pyramidal neurons transfected with a plasmid encoding a small hairpin RNA (shRNA) to knockdown endogenous Mecp2 had shorter dendrites than control untransfected neurons, without detectable changes in axonal morphology. On the other hand, overexpression of wildtype (wt) human MECP2 increased dendritic branching, in addition to axonal branching and length. Consistent with reduced neuronal growth and complexity in Rett syndrome (RTT) brains, overexpression of human MECP2 carrying missense mutations common in RTT individuals (R106W or T158M) reduced dendritic and axonal length. One of the targets of MeCP2 transcriptional control is the Bdnf gene. Indeed, endogenous Mecp2 knockdown increased the intracellular levels of BDNF protein compared to untransfected neurons, suggesting that MeCP2 represses Bdnf transcription. Surprisingly, overexpression of wt MECP2 also increased BDNF levels, while overexpression of RTT-associated MECP2 mutants failed to affect BDNF levels. The extracellular BDNF scavenger TrkB-Fc prevented dendritic overgrowth in wt MECP2-overexpressing neurons, while overexpression of the Bdnf gene reverted the dendritic atrophy caused by Mecp2-knockdown. However, this effect was only partial, since Bdnf increased dendritic length only to control levels in mutant MECP2-overexpressing neurons, but not as much as in Bdnf-transfected cells. Our results demonstrate that MeCP2 plays varied roles in dendritic and axonal development during neuronal terminal differentiation, and that some of these effects are mediated by autocrine actions of BDNF.

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Year:  2009        PMID: 19217433      PMCID: PMC2726722          DOI: 10.1016/j.nbd.2008.12.011

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  98 in total

1.  Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome.

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2.  Increased dendritic complexity and axonal length in cultured mouse cortical neurons overexpressing methyl-CpG-binding protein MeCP2.

Authors:  Denis G M Jugloff; Benjamin P Jung; Diana Purushotham; Richard Logan; James H Eubanks
Journal:  Neurobiol Dis       Date:  2005 Jun-Jul       Impact factor: 5.996

3.  DNA binding selectivity of MeCP2 due to a requirement for A/T sequences adjacent to methyl-CpG.

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Journal:  Mol Cell       Date:  2005-09-02       Impact factor: 17.970

Review 4.  MeCP2 expression and function during brain development: implications for Rett syndrome's pathogenesis and clinical evolution.

Authors:  Walter E Kaufmann; Michael V Johnston; Mary E Blue
Journal:  Brain Dev       Date:  2005-09-22       Impact factor: 1.961

5.  Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome.

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Review 7.  MeCP2 in neurons: closing in on the causes of Rett syndrome.

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Review 8.  Rett syndrome: model of neurodevelopmental disorders.

Authors:  Alan K Percy; Jane B Lane
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10.  The impact of MECP2 mutations in the expression patterns of Rett syndrome patients.

Authors:  Esteban Ballestar; Santiago Ropero; Miguel Alaminos; Judith Armstrong; Fernando Setien; Ruben Agrelo; Mario F Fraga; Michel Herranz; Sonia Avila; Mercedes Pineda; Eugenia Monros; Manel Esteller
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  58 in total

Review 1.  Complexities of Rett syndrome and MeCP2.

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2.  Normal mitral cell dendritic development in the setting of Mecp2 mutation.

Authors:  A M Palmer; A L Degano; M J Park; S Ramamurthy; G V Ronnett
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3.  Exercise impacts brain-derived neurotrophic factor plasticity by engaging mechanisms of epigenetic regulation.

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4.  Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations.

Authors:  Christopher A Chapleau; Gaston D Calfa; Meredith C Lane; Asher J Albertson; Jennifer L Larimore; Shinichi Kudo; Dawna L Armstrong; Alan K Percy; Lucas Pozzo-Miller
Journal:  Neurobiol Dis       Date:  2009-05-12       Impact factor: 5.996

Review 5.  Rett syndrome: exploring the autism link.

Authors:  Alan K Percy
Journal:  Arch Neurol       Date:  2011-08

Review 6.  Experimental models of Rett syndrome based on Mecp2 dysfunction.

Authors:  Gaston Calfa; Alan K Percy; Lucas Pozzo-Miller
Journal:  Exp Biol Med (Maywood)       Date:  2011-01

Review 7.  MicroRNAs in addiction: adaptation's middlemen?

Authors:  M D Li; A D van der Vaart
Journal:  Mol Psychiatry       Date:  2011-05-24       Impact factor: 15.992

Review 8.  Epigenetic modulation during hippocampal development.

Authors:  Si-Jing Fan; An-Bang Sun; Lian Liu
Journal:  Biomed Rep       Date:  2018-10-18

9.  Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism.

Authors:  Christopher A Chapleau; Jennifer L Larimore; Anne Theibert; Lucas Pozzo-Miller
Journal:  J Neurodev Disord       Date:  2009-09       Impact factor: 4.025

10.  MeCP2 controls BDNF expression and cocaine intake through homeostatic interactions with microRNA-212.

Authors:  Heh-In Im; Jonathan A Hollander; Purva Bali; Paul J Kenny
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