Literature DB >> 23278576

Synaptic basal lamina-associated congenital myasthenic syndromes.

Ricardo A Maselli1, Juan Arredondo, Michael J Ferns, Robert L Wollmann.   

Abstract

Proteins associated with the basal lamina (BL) participate in complex signal transduction processes that are essential for the development and maintenance of the neuromuscular junction (NMJ). Most important junctional BL proteins are collagens, such as collagen IV (α3-6), collagen XIII, and ColQ; laminins; nidogens; and heparan sulfate proteoglycans, such as perlecan and agrin. Mice lacking Colq (Colq(-/-)), laminin β2 (Lamb2(-/-)), or collagen XIII (Col13a1(-/-)) show immature nerve terminals enwrapped by Schwann cell projections that invaginate into the synaptic cleft and decrease contact surface for neurotransmission. Human mutations in COLQ, LAMB2, and AGRN cause congenital myasthenic syndromes (CMSs) owing to deficiency of ColQ, laminin-β2, and agrin, respectively. In these syndromes the NMJ ultrastructure shows striking resemblance to that of mice lacking the corresponding protein; furthermore, the extracellular localization of mutant proteins may provide favorable conditions for replacement strategies based on gene therapy and stem cells.
© 2012 New York Academy of Sciences.

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Year:  2012        PMID: 23278576     DOI: 10.1111/j.1749-6632.2012.06807.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  13 in total

1.  Pathogenic effects of agrin V1727F mutation are isoform specific and decrease its expression and affinity for HSPGs and LRP4.

Authors:  John B Rudell; Ricardo A Maselli; Vladimir Yarov-Yarovoy; Michael J Ferns
Journal:  Hum Mol Genet       Date:  2019-08-15       Impact factor: 6.150

2.  The Clinical and Genetic Features in Chinese Children With Steroid-Resistant or Early-Onset Nephrotic Syndrome: A Multicenter Cohort Study.

Authors:  Xiujuan Zhu; Yanqin Zhang; Zihua Yu; Li Yu; Wenyan Huang; Shuzhen Sun; Yingjie Li; Mo Wang; Yongzhen Li; Liangzhong Sun; Qing Yang; Fang Deng; Xiaoshan Shao; Ling Liu; Cuihua Liu; Yuanhan Qin; Shipin Feng; Hongtao Zhu; Fang Yang; Weimin Zheng; Wanqi Zheng; Rirong Zhong; Ling Hou; Jianhua Mao; Fang Wang; Jie Ding
Journal:  Front Med (Lausanne)       Date:  2022-06-09

3.  COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina.

Authors:  Juan Arredondo; Marian Lara; Fiona Ng; Danielle A Gochez; Diana C Lee; Stephanie P Logia; Joanna Nguyen; Ricardo A Maselli
Journal:  Hum Genet       Date:  2013-11-27       Impact factor: 4.132

Review 4.  How to Spot Congenital Myasthenic Syndromes Resembling the Lambert-Eaton Myasthenic Syndrome? A Brief Review of Clinical, Electrophysiological, and Genetics Features.

Authors:  Paulo José Lorenzoni; Rosana Herminia Scola; Claudia Suemi Kamoi Kay; Lineu Cesar Werneck; Rita Horvath; Hanns Lochmüller
Journal:  Neuromolecular Med       Date:  2018-04-25       Impact factor: 3.843

5.  Roles of the synaptic molecules Hevin and SPARC in mouse neuromuscular junction development and repair.

Authors:  Vanessa L Brayman; Thomas Taetzsch; MacKenzie Miko; Shreyaska Dahal; W Christopher Risher; Gregorio Valdez
Journal:  Neurosci Lett       Date:  2021-01-22       Impact factor: 3.046

6.  Endplate denervation correlates with Nogo-A muscle expression in amyotrophic lateral sclerosis patients.

Authors:  Gaëlle Bruneteau; Stéphanie Bauché; Jose Luis Gonzalez de Aguilar; Guy Brochier; Nathalie Mandjee; Marie-Laure Tanguy; Ghulam Hussain; Anthony Behin; Frédéric Khiami; Elhadi Sariali; Caroline Hell-Remy; François Salachas; Pierre-François Pradat; Lucette Lacomblez; Sophie Nicole; Bertrand Fontaine; Michel Fardeau; Jean-Philippe Loeffler; Vincent Meininger; Emmanuel Fournier; Jeanine Koenig; Daniel Hantaï
Journal:  Ann Clin Transl Neurol       Date:  2015-02-16       Impact factor: 4.511

7.  Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain.

Authors:  Clare V Logan; Judith Cossins; Pedro M Rodríguez Cruz; David A Parry; Susan Maxwell; Pilar Martínez-Martínez; Joey Riepsaame; Zakia A Abdelhamed; Alice V R Lake; Maria Moran; Stephanie Robb; Gabriel Chow; Caroline Sewry; Philip M Hopkins; Eamonn Sheridan; Sandeep Jayawant; Jacqueline Palace; Colin A Johnson; David Beeson
Journal:  Am J Hum Genet       Date:  2015-11-25       Impact factor: 11.025

8.  Motor function recovery: deciphering a regenerative niche at the neuromuscular synapse.

Authors:  Diego Zelada; Francisca Bermedo-García; Nicolás Collao; Juan P Henríquez
Journal:  Biol Rev Camb Philos Soc       Date:  2020-12-17

9.  Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome.

Authors:  Gina L O'Grady; Corien Verschuuren; Michaela Yuen; Richard Webster; Manoj Menezes; Johanna M Fock; Natalie Pride; Heather A Best; Tatiana Benavides Damm; Christian Turner; Monkol Lek; Andrew G Engel; Kathryn N North; Nigel F Clarke; Daniel G MacArthur; Erik-Jan Kamsteeg; Sandra T Cooper
Journal:  Neurology       Date:  2016-09-02       Impact factor: 9.910

10.  Myasthenia Gravis: From the Viewpoint of Pathogenicity Focusing on Acetylcholine Receptor Clustering, Trans-Synaptic Homeostasis and Synaptic Stability.

Authors:  Masaharu Takamori
Journal:  Front Mol Neurosci       Date:  2020-05-28       Impact factor: 5.639

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