Altered gene expression levels of genes related to muscle function in adults with cerebral palsy
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Altered gene expression levels of genes related to muscle function in adults with cerebral palsy. / Pingel, Jessica; Vandenrijt, Jasper; Kampmann, Marie Louise; Andersen, Jeppe Dyrberg.
In: Tissue and Cell, Vol. 76, 101744, 2022.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Altered gene expression levels of genes related to muscle function in adults with cerebral palsy
AU - Pingel, Jessica
AU - Vandenrijt, Jasper
AU - Kampmann, Marie Louise
AU - Andersen, Jeppe Dyrberg
N1 - Funding Information: This project was funded by the Danish research Council ( DFF-1333-00197 ), and the Elsass Foundation . Publisher Copyright: © 2022
PY - 2022
Y1 - 2022
N2 - Cerebral palsy (CP) is the most common cause of movement disorders in children. Next generation sequencing (NGS) studies have previously shown that expression levels are fundamentally different in children with CP compared to typically developing (TD). However, given that children are in full development, we might expect gene expression levels to change once maturity is reached. Therefore, the main purpose of this study was to investigate gene expression levels of 93 target genes in adults with CP using NGS on muscle biopsies of the gastrocnemius, taken from 22 participants (n = 12 adults with CP; n = 10 TD adults). Subsequently, we carried out NGS of the mitochondrial genome to identify mtDNA variants, and additionally we studied the mitochondrial content using transmission electron microscopy images of the gastrocnemius muscle. Finally, we compared systemic ion levels between TD adults and adults with CP. Differential gene expression levels were found in genes involved in muscle contraction (MYH1 and MYBPC2), mitochondrial function kATP5J, CYCS and NDUFB6), calcium handling (CAMK2B and ATP2A), metabolism (LPL), muscle signaling (MYC, CREB1, ACVR2B, LMNA and TRIM54), and ECM (TNC). There was no statistical significant difference between CP and TD for mtDNA variant frequencies and mitochondrial content. The ion levels of Ca2+, Na+ and K+ were statistically significantly reduced while the Cl− levels were significant increased in adults with CP compared to TD adults. These results highlight that most transcriptional differences are related to muscle function in adults with CP and that mitochondrial function might be altered but not mitochondrial content.
AB - Cerebral palsy (CP) is the most common cause of movement disorders in children. Next generation sequencing (NGS) studies have previously shown that expression levels are fundamentally different in children with CP compared to typically developing (TD). However, given that children are in full development, we might expect gene expression levels to change once maturity is reached. Therefore, the main purpose of this study was to investigate gene expression levels of 93 target genes in adults with CP using NGS on muscle biopsies of the gastrocnemius, taken from 22 participants (n = 12 adults with CP; n = 10 TD adults). Subsequently, we carried out NGS of the mitochondrial genome to identify mtDNA variants, and additionally we studied the mitochondrial content using transmission electron microscopy images of the gastrocnemius muscle. Finally, we compared systemic ion levels between TD adults and adults with CP. Differential gene expression levels were found in genes involved in muscle contraction (MYH1 and MYBPC2), mitochondrial function kATP5J, CYCS and NDUFB6), calcium handling (CAMK2B and ATP2A), metabolism (LPL), muscle signaling (MYC, CREB1, ACVR2B, LMNA and TRIM54), and ECM (TNC). There was no statistical significant difference between CP and TD for mtDNA variant frequencies and mitochondrial content. The ion levels of Ca2+, Na+ and K+ were statistically significantly reduced while the Cl− levels were significant increased in adults with CP compared to TD adults. These results highlight that most transcriptional differences are related to muscle function in adults with CP and that mitochondrial function might be altered but not mitochondrial content.
KW - Cerebral palsy
KW - Contractures
KW - Ions
KW - Mitochondria
KW - mRNA sequencing
U2 - 10.1016/j.tice.2022.101744
DO - 10.1016/j.tice.2022.101744
M3 - Journal article
C2 - 35151178
AN - SCOPUS:85124282587
VL - 76
JO - Tissue and Cell
JF - Tissue and Cell
SN - 0040-8166
M1 - 101744
ER -
ID: 298032810