Literature DB >> 21505075

Peripheral nerve pathology, including aberrant Schwann cell differentiation, is ameliorated by doxycycline in a laminin-α2-deficient mouse model of congenital muscular dystrophy.

Sachiko Homma1, Mary Lou Beermann, Jeffrey Boone Miller.   

Abstract

The most common form of childhood congenital muscular dystrophy, Type 1A (MDC1A), is caused by mutations in the human LAMA2 gene that encodes the laminin-α2 subunit. In addition to skeletal muscle deficits, MDC1A patients typically show a loss of peripheral nerve function. To identify the mechanisms underlying this loss of nerve function, we have examined pathology and cell differentiation in sciatic nerves and ventral roots of the laminin-α2-deficient (Lama2(-/-)) mice, which are models for MDC1A. We found that, compared with wild-type, sciatic nerves of Lama2(-/-) mice had a significant increase in both proliferating (Ki67+) cells and premyelinating (Oct6+) Schwann cells, but also had a significant decrease in both immature/non-myelinating [glial fibrillary acidic protein (GFAP)(+)] and myelinating (Krox20+) Schwann cells. To extend our previous work in which we found that doxycycline, which has multiple effects on mammalian cells, improves motor behavior and more than doubles the median life-span of Lama2(-/-) mice, we also determined how nerve pathology was affected by doxycycline treatment. We found that myelinating (Krox20+) Schwann cells were significantly increased in doxycycline-treated compared with untreated sciatic nerves. In addition, doxycycline-treated peripheral nerves had significantly less pathology as measured by assays such as amount of unmyelinated or disorganized axons. This study thus identified aberrant proliferation and differentiation of Schwann cells as key components of pathogenesis in peripheral nerves and provided proof-of-concept that pharmaceutical therapy can be of potential benefit for peripheral nerve dysfunction in MDC1A.

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Year:  2011        PMID: 21505075      PMCID: PMC3110004          DOI: 10.1093/hmg/ddr168

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  53 in total

Review 1.  The congenital muscular dystrophies in 2004: a century of exciting progress.

Authors:  Francesco Muntoni; Thomas Voit
Journal:  Neuromuscul Disord       Date:  2004-10       Impact factor: 4.296

Review 2.  Effect of doxycycline on atherosclerosis: from bench to bedside.

Authors:  Gastón A Rodriguez-Granillo; Agustina Rodriguez-Granillo; José Milei
Journal:  Recent Pat Cardiovasc Drug Discov       Date:  2011-01

3.  Schwann cell myelination occurred without basal lamina formation in laminin alpha2 chain-null mutant (dy3K/dy3K) mice.

Authors:  M Nakagawa; Y Miyagoe-Suzuki; K Ikezoe; Y Miyata; I Nonaka; K Harii; S Takeda
Journal:  Glia       Date:  2001-08       Impact factor: 7.452

4.  An agrin minigene rescues dystrophic symptoms in a mouse model for congenital muscular dystrophy.

Authors:  J Moll; P Barzaghi; S Lin; G Bezakova; H Lochmüller; E Engvall; U Müller; M A Ruegg
Journal:  Nature       Date:  2001-09-20       Impact factor: 49.962

5.  Proteasome inhibition improves the muscle of laminin α2 chain-deficient mice.

Authors:  Virginie Carmignac; Ronan Quéré; Madeleine Durbeej
Journal:  Hum Mol Genet       Date:  2010-11-17       Impact factor: 6.150

6.  Complement 3 deficiency and oral prednisolone improve strength and prolong survival of laminin alpha2-deficient mice.

Authors:  Anne M Connolly; Richard M Keeling; Elizabeth M Streif; Alan Pestronk; Shobhna Mehta
Journal:  J Neuroimmunol       Date:  2002-06       Impact factor: 3.478

7.  Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice.

Authors:  L T Guo; X U Zhang; W Kuang; H Xu; L A Liu; J-T Vilquin; Y Miyagoe-Suzuki; S Takeda; M A Ruegg; U M Wewer; E Engvall
Journal:  Neuromuscul Disord       Date:  2003-03       Impact factor: 4.296

8.  Disruption of ErbB receptor signaling in adult non-myelinating Schwann cells causes progressive sensory loss.

Authors:  Suzhen Chen; Carlos Rio; Ru-Rong Ji; Pieter Dikkes; Richard E Coggeshall; Clifford J Woolf; Gabriel Corfas
Journal:  Nat Neurosci       Date:  2003-10-12       Impact factor: 24.884

9.  Laminin alpha1 chain reduces muscular dystrophy in laminin alpha2 chain deficient mice.

Authors:  Kinga Gawlik; Yuko Miyagoe-Suzuki; Peter Ekblom; Shin'ichi Takeda; Madeleine Durbeej
Journal:  Hum Mol Genet       Date:  2004-06-22       Impact factor: 6.150

10.  Laminin gamma1 is critical for Schwann cell differentiation, axon myelination, and regeneration in the peripheral nerve.

Authors:  Zu-Lin Chen; Sidney Strickland
Journal:  J Cell Biol       Date:  2003-11-24       Impact factor: 10.539

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  5 in total

1.  Aberrant Caspase Activation in Laminin-α2-Deficient Human Myogenic Cells is Mediated by p53 and Sirtuin Activity.

Authors:  Soonsang Yoon; Mary Lou Beermann; Bryant Yu; Di Shao; Markus Bachschmid; Jeffrey Boone Miller
Journal:  J Neuromuscul Dis       Date:  2018

Review 2.  A Family of Laminin α2 Chain-Deficient Mouse Mutants: Advancing the Research on LAMA2-CMD.

Authors:  Kinga I Gawlik; Madeleine Durbeej
Journal:  Front Mol Neurosci       Date:  2020-04-21       Impact factor: 5.639

3.  Tetracyclines and neuromuscular disorders.

Authors:  Daniele Orsucci; Michelangelo Mancuso; Massimiliano Filosto; Gabriele Siciliano
Journal:  Curr Neuropharmacol       Date:  2012-06       Impact factor: 7.363

4.  Amelioration of Muscle and Nerve Pathology in LAMA2 Muscular Dystrophy by AAV9-Mini-Agrin.

Authors:  Chunping Qiao; Yi Dai; Viktoriya D Nikolova; Quan Jin; Jianbin Li; Bin Xiao; Juan Li; Sheryl S Moy; Xiao Xiao
Journal:  Mol Ther Methods Clin Dev       Date:  2018-01-31       Impact factor: 6.698

5.  Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models.

Authors:  Andrea J Arreguin; Holly Colognato
Journal:  Front Mol Neurosci       Date:  2020-07-23       Impact factor: 5.639

  5 in total

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