Literature DB >> 8363059

Development of innervation of skeletal muscle fibers in man: relation to acetylcholine receptors.

L F Hesselmans1, F G Jennekens, C J Van den Oord, H Veldman, A Vincent.   

Abstract

The aim of this study was to establish the time scale of developmental changes in innervation of skeletal muscle fibers in man. Specimens of thigh and intercostal muscle from 19 embryos and 18 infants were examined with histological methods which enabled the discrimination between fetal (gamma) and adult (epsilon) types of acetylcholine receptors (AChRs). At 8 weeks of development, AChRs were distributed diffusely in the myotube membranes. Following onset of innervation in approximately the ninth week the length of the AChR positive area diminished and reached its shortest size at the sixteenth developmental week. At the sixteenth and eighteenth week some nerve terminals opposed the muscle membrane outside the AChR positive area. Decrease in the number of nerve terminals, strongly suggesting elimination of polyneuronal innervation, started in the sixteenth week and was completed in the twenty-fifth week. This fetal (gamma) type of AChR could no longer be demonstrated after the thirty-first week. The length of the end-plates as determined by the presence of AChRs increased again in the last week before birth and reached a plateau size by the end of the first year after birth. It is concluded that in man the transition from poly- to mononeuronal innervation takes place between the sixteenth and twenty-fifth weeks of development. The evidence available suggests that the retraction of nerve terminals is preceded by loss of AChRs from the muscle membrane facing the terminals. There is no relationship between retraction of nerve terminals and the switch from fetal to adult type of AChR. The size of the presynaptic apparatus changes little after the first year of life.

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Year:  1993        PMID: 8363059     DOI: 10.1002/ar.1092360315

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  36 in total

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2.  A comparison of MyoD1 and fetal acetylcholine receptor expression in childhood tumors and normal tissues: implications for the molecular diagnosis of minimal disease in rhabdomyosarcomas.

Authors:  S Gattenloehner; B Dockhorn-Dworniczak; I Leuschner; A Vincent; H K Müller-Hermelink; A Marx
Journal:  J Mol Diagn       Date:  1999-11       Impact factor: 5.568

3.  Expression of intermediate filaments at muscle insertions in human fetuses.

Authors:  Shinichi Abe; Sun-ki Rhee; Makoto Osonoi; Takuo Nakamura; Baik Hwan Cho; Gen Murakami; Yoshinobu Ide
Journal:  J Anat       Date:  2010-05-25       Impact factor: 2.610

4.  Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome.

Authors:  Neil V Morgan; Louise A Brueton; Phillip Cox; Marie T Greally; John Tolmie; Shanaz Pasha; Irene A Aligianis; Hans van Bokhoven; Tamas Marton; Lihadh Al-Gazali; Jenny E V Morton; Christine Oley; Colin A Johnson; Richard C Trembath; Han G Brunner; Eamonn R Maher
Journal:  Am J Hum Genet       Date:  2006-06-20       Impact factor: 11.025

5.  Neuromotor synapses in Escobar syndrome.

Authors:  Karyn G Robinson; Matthew J Viereck; Megan V Margiotta; Karen W Gripp; Omar A Abdul-Rahman; Robert E Akins
Journal:  Am J Med Genet A       Date:  2013-08-16       Impact factor: 2.802

6.  The fetal form of the acetylcholine receptor distinguishes rhabdomyosarcomas from other childhood tumors.

Authors:  S Gattenloehner; A Vincent; I Leuschner; S Tzartos; H K Müller-Hermelink; T Kirchner; A Marx
Journal:  Am J Pathol       Date:  1998-02       Impact factor: 4.307

7.  Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit.

Authors:  Katrin Hoffmann; Juliane S Muller; Sigmar Stricker; Andre Megarbane; Anna Rajab; Tom H Lindner; Monika Cohen; Eliane Chouery; Lynn Adaimy; Ismat Ghanem; Valerie Delague; Eugen Boltshauser; Beril Talim; Rita Horvath; Peter N Robinson; Hanns Lochmüller; Christoph Hübner; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2006-06-20       Impact factor: 11.025

Review 8.  Current status of the congenital myasthenic syndromes.

Authors:  Andrew G Engel
Journal:  Neuromuscul Disord       Date:  2011-11-21       Impact factor: 4.296

9.  Plasma from human mothers of fetuses with severe arthrogryposis multiplex congenita causes deformities in mice.

Authors:  L Jacobson; A Polizzi; G Morriss-Kay; A Vincent
Journal:  J Clin Invest       Date:  1999-04       Impact factor: 14.808

10.  Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.

Authors:  Stéphanie Bauché; Seana O'Regan; Yoshiteru Azuma; Fanny Laffargue; Grace McMacken; Damien Sternberg; Guy Brochier; Céline Buon; Nassima Bouzidi; Ana Topf; Emmanuelle Lacène; Ganaelle Remerand; Anne-Marie Beaufrere; Céline Pebrel-Richard; Julien Thevenon; Salima El Chehadeh-Djebbar; Laurence Faivre; Yannis Duffourd; Federica Ricci; Tiziana Mongini; Chiara Fiorillo; Guja Astrea; Carmen Magdalena Burloiu; Niculina Butoianu; Carmen Sandu; Laurent Servais; Gisèle Bonne; Isabelle Nelson; Isabelle Desguerre; Marie-Christine Nougues; Benoit Bœuf; Norma Romero; Jocelyn Laporte; Anne Boland; Doris Lechner; Jean-François Deleuze; Bertrand Fontaine; Laure Strochlic; Hanns Lochmuller; Bruno Eymard; Michèle Mayer; Sophie Nicole
Journal:  Am J Hum Genet       Date:  2016-08-25       Impact factor: 11.025

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