Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons

Abstract Insight into the bidirectional signaling between primary human myogenic cells and neurons is lacking. For this purpose, human myogenic cells were derived from the semitendinosus and gracilis muscles of five healthy individuals and co‐cultured with cerebellar granule neurons from two litters...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Michal Tamáš, Stanislava Pankratova, Peter Schjerling, Casper Soendenbroe, Ching‐Yan Chloé Yeung, Cristian Pablo Pennisi, Jens R. Jakobsen, Michael R. Krogsgaard, Michael Kjaer, Abigail L. Mackey
Formato: article
Lenguaje:EN
Publicado: Wiley 2021
Materias:
Acceso en línea:https://doaj.org/article/74cb20f03038431e9c90762e3b383d57
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:74cb20f03038431e9c90762e3b383d57
record_format dspace
spelling oai:doaj.org-article:74cb20f03038431e9c90762e3b383d572021-11-15T09:54:40ZMutual stimulatory signaling between human myogenic cells and rat cerebellar neurons2051-817X10.14814/phy2.15077https://doaj.org/article/74cb20f03038431e9c90762e3b383d572021-11-01T00:00:00Zhttps://doi.org/10.14814/phy2.15077https://doaj.org/toc/2051-817XAbstract Insight into the bidirectional signaling between primary human myogenic cells and neurons is lacking. For this purpose, human myogenic cells were derived from the semitendinosus and gracilis muscles of five healthy individuals and co‐cultured with cerebellar granule neurons from two litters of 7‐day‐old Wistar rat pups, in muscle medium or neural medium, alongside monocultures of myogenic cells or neurons. RT‐PCR was performed to determine human mRNA levels of GAPDH, Ki67, myogenin, and MUSK, and the acetylcholine receptor subtypes CHRNA1, CHRNB1, CHRNG, CHRND, and CHRNE, and rat mRNA levels of GAPDH, Fth1, Rack1, vimentin, Cdh13, and Ppp1r1a. Immunocytochemistry was used to evaluate neurite outgrowth (GAP43) in the presence and absence of myogenic cells. Co‐culture with primary neurons lead to higher myogenic cell gene expression levels of GAPDH, myogenin, MUSK, CHRNA1, CHRNG, and CHRND, compared to myogenic cells cultured alone. It appeared that neurons preferentially attached to myotubes and that neurite outgrowth was enhanced when neurons were cultured with myogenic cells compared to monoculture. In neural medium, rat mRNA levels of GAPDH, vimentin, Cdh13, and Ppp1r1a were greater in co‐culture, versus monoculture, whereas in muscle medium co‐culture lead to lower levels of Fth1, Rack1, vimentin, and Cdh13 than monoculture. These findings demonstrate mutually beneficial stimulatory signaling between rat cerebellar granule neurons and human myogenic cells, providing support for an active role for both the neuron and the muscle cell in stimulating neurite growth and myogenesis. Bidirectional muscle nerve signaling.Michal TamášStanislava PankratovaPeter SchjerlingCasper SoendenbroeChing‐Yan Chloé YeungCristian Pablo PennisiJens R. JakobsenMichael R. KrogsgaardMichael KjaerAbigail L. MackeyWileyarticleacetylcholine receptorinnervationmyogenesisneuronskeletal musclePhysiologyQP1-981ENPhysiological Reports, Vol 9, Iss 21, Pp n/a-n/a (2021)
institution DOAJ
collection DOAJ
language EN
topic acetylcholine receptor
innervation
myogenesis
neuron
skeletal muscle
Physiology
QP1-981
spellingShingle acetylcholine receptor
innervation
myogenesis
neuron
skeletal muscle
Physiology
QP1-981
Michal Tamáš
Stanislava Pankratova
Peter Schjerling
Casper Soendenbroe
Ching‐Yan Chloé Yeung
Cristian Pablo Pennisi
Jens R. Jakobsen
Michael R. Krogsgaard
Michael Kjaer
Abigail L. Mackey
Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
description Abstract Insight into the bidirectional signaling between primary human myogenic cells and neurons is lacking. For this purpose, human myogenic cells were derived from the semitendinosus and gracilis muscles of five healthy individuals and co‐cultured with cerebellar granule neurons from two litters of 7‐day‐old Wistar rat pups, in muscle medium or neural medium, alongside monocultures of myogenic cells or neurons. RT‐PCR was performed to determine human mRNA levels of GAPDH, Ki67, myogenin, and MUSK, and the acetylcholine receptor subtypes CHRNA1, CHRNB1, CHRNG, CHRND, and CHRNE, and rat mRNA levels of GAPDH, Fth1, Rack1, vimentin, Cdh13, and Ppp1r1a. Immunocytochemistry was used to evaluate neurite outgrowth (GAP43) in the presence and absence of myogenic cells. Co‐culture with primary neurons lead to higher myogenic cell gene expression levels of GAPDH, myogenin, MUSK, CHRNA1, CHRNG, and CHRND, compared to myogenic cells cultured alone. It appeared that neurons preferentially attached to myotubes and that neurite outgrowth was enhanced when neurons were cultured with myogenic cells compared to monoculture. In neural medium, rat mRNA levels of GAPDH, vimentin, Cdh13, and Ppp1r1a were greater in co‐culture, versus monoculture, whereas in muscle medium co‐culture lead to lower levels of Fth1, Rack1, vimentin, and Cdh13 than monoculture. These findings demonstrate mutually beneficial stimulatory signaling between rat cerebellar granule neurons and human myogenic cells, providing support for an active role for both the neuron and the muscle cell in stimulating neurite growth and myogenesis. Bidirectional muscle nerve signaling.
format article
author Michal Tamáš
Stanislava Pankratova
Peter Schjerling
Casper Soendenbroe
Ching‐Yan Chloé Yeung
Cristian Pablo Pennisi
Jens R. Jakobsen
Michael R. Krogsgaard
Michael Kjaer
Abigail L. Mackey
author_facet Michal Tamáš
Stanislava Pankratova
Peter Schjerling
Casper Soendenbroe
Ching‐Yan Chloé Yeung
Cristian Pablo Pennisi
Jens R. Jakobsen
Michael R. Krogsgaard
Michael Kjaer
Abigail L. Mackey
author_sort Michal Tamáš
title Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
title_short Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
title_full Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
title_fullStr Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
title_full_unstemmed Mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
title_sort mutual stimulatory signaling between human myogenic cells and rat cerebellar neurons
publisher Wiley
publishDate 2021
url https://doaj.org/article/74cb20f03038431e9c90762e3b383d57
work_keys_str_mv AT michaltamas mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT stanislavapankratova mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT peterschjerling mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT caspersoendenbroe mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT chingyanchloeyeung mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT cristianpablopennisi mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT jensrjakobsen mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT michaelrkrogsgaard mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT michaelkjaer mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
AT abigaillmackey mutualstimulatorysignalingbetweenhumanmyogeniccellsandratcerebellarneurons
_version_ 1718428442419003392