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ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 control myogenic differentiation of skeletal muscle satellite cells by retinoic acid-dependent and -independent mechanisms
by
Krabichler, Florian
, Wu, Wei
, Franzmeier, Sophie
, Koch, Marco
, Steingruber, Laura
, Schlegel, Jürgen
in
Aldehyde dehydrogenase
/ Aldehydes
/ autophagosomes
/ Autophagy
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ Cell cycle
/ Cell differentiation
/ Cell lines
/ CRISPR
/ Dehydrogenases
/ Disulfiram
/ Enzymatic activity
/ enzyme activity
/ Enzymes
/ Human Genetics
/ mice
/ Molecular Medicine
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Neomycin
/ Proteomics
/ Regular Article
/ Retinoic acid
/ Satellite cells
/ Skeletal muscle
/ Tretinoin
2023
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ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 control myogenic differentiation of skeletal muscle satellite cells by retinoic acid-dependent and -independent mechanisms
by
Krabichler, Florian
, Wu, Wei
, Franzmeier, Sophie
, Koch, Marco
, Steingruber, Laura
, Schlegel, Jürgen
in
Aldehyde dehydrogenase
/ Aldehydes
/ autophagosomes
/ Autophagy
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ Cell cycle
/ Cell differentiation
/ Cell lines
/ CRISPR
/ Dehydrogenases
/ Disulfiram
/ Enzymatic activity
/ enzyme activity
/ Enzymes
/ Human Genetics
/ mice
/ Molecular Medicine
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Neomycin
/ Proteomics
/ Regular Article
/ Retinoic acid
/ Satellite cells
/ Skeletal muscle
/ Tretinoin
2023
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ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 control myogenic differentiation of skeletal muscle satellite cells by retinoic acid-dependent and -independent mechanisms
by
Krabichler, Florian
, Wu, Wei
, Franzmeier, Sophie
, Koch, Marco
, Steingruber, Laura
, Schlegel, Jürgen
in
Aldehyde dehydrogenase
/ Aldehydes
/ autophagosomes
/ Autophagy
/ Biomedical and Life Sciences
/ Biomedicine
/ blood serum
/ Cell cycle
/ Cell differentiation
/ Cell lines
/ CRISPR
/ Dehydrogenases
/ Disulfiram
/ Enzymatic activity
/ enzyme activity
/ Enzymes
/ Human Genetics
/ mice
/ Molecular Medicine
/ muscle development
/ Muscles
/ Musculoskeletal system
/ Myoblasts
/ Myogenesis
/ Neomycin
/ Proteomics
/ Regular Article
/ Retinoic acid
/ Satellite cells
/ Skeletal muscle
/ Tretinoin
2023
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ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 control myogenic differentiation of skeletal muscle satellite cells by retinoic acid-dependent and -independent mechanisms
Journal Article
ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 control myogenic differentiation of skeletal muscle satellite cells by retinoic acid-dependent and -independent mechanisms
2023
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Overview
ALDH1A1 and ALDH1A3 paralogues of aldehyde dehydrogenase 1 (ALDH1) control myogenic differentiation of skeletal muscle satellite cells (SC) by formation of retinoic acid (RA) and subsequent cell cycle adjustments. The respective relevance of each paralogue for myogenic differentiation and the mechanistic interaction of each paralogue within RA-dependent and RA-independent pathways remain elusive.
We analysed the impact of ALDH1A1 and ALDH1A3 activity on myogenesis of murine C2C12 myoblasts. Both paralogues are pivotal factors in myogenic differentiation, since CRISPR/Cas9-edited single paralogue knock-out impaired serum withdrawal-induced myogenic differentiation, while successive recombinant re-expression of ALDH1A1 or ALDH1A3, respectively, in the corresponding ALDH1 paralogue single knock-out cell lines, recovered the differentiation potential. Loss of differentiation in single knock-out cell lines was restored by treatment with RA-analogue TTNPB, while RA-receptor antagonization by AGN 193109 inhibited differentiation of wildtype cell lines, supporting the idea that RA-dependent pathway is pivotal for myogenic differentiation which is accomplished by both paralogues.
However, overexpression of ALDH1-paralogues or disulfiram-mediated inhibition of ALDH1 enzymatic activity not only increased ALDH1A1 and ALDH1A3 protein levels but also induced subsequent differentiation of C2C12 myoblasts independently from serum withdrawal, indicating that ALDH1-dependent myogenic differentiation relies on different cellular conditions. Remarkably, ALDH1-paralogue knock-out impaired the autophagic flux, namely autophagosome cargo protein p62 formation and LC3B-I to LC3B-II conversion, demonstrating that ALDH1-paralogues interact with autophagy in myogenesis. Together, ALDH1 paralogues play a crucial role in myogenesis by orchestration of complex RA-dependent and RA-independent pathways.
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