Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes

Chih Yuan Fang, Mien Cheng Chen, Tzu Hao Chang, Chia Chen Wu, Jen Ping Chang, Hsien Da Huang, Wan Chun Ho, Yi Zhen Wang, Kuo Li Pan, Yu Sheng Lin, Yao Kuang Huang, Chien Jen Chen, Wei Chieh Lee

Research output: Contribution to journalArticle

Abstract

Background: Lipid expression is increased in the atrial myocytes of mitral regurgitation (MR) patients. This study aimed to investigate key regulatory genes and mechanisms of atrial lipotoxic myopathy in MR. Methods: The HL-1 atrial myocytes were subjected to uniaxial cyclic stretching for eight hours. Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism were analyzed by PCR assay (168 genes). Results: The stretched myocytes had significantly larger cell size and higher lipid expression than non-stretched myocytes (all p < 0.001). Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism in the myocytes were analyzed by PCR assay (168 genes). In comparison with their counterparts in non-stretched myocytes, seven genes in stretched monocytes (Idi1, Olr1, Nr1h4, Fabp2, Prkag3, Slc27a5, Fabp6) revealed differential upregulation with an altered fold change >1.5. Nine genes in stretched monocytes (Apoa4, Hmgcs2, Apol8, Srebf1, Acsm4, Fabp1, Acox2, Acsl6, Gk) revealed differential downregulation with an altered fold change <0.67. Canonical pathway analysis, using Ingenuity Pathway Analysis software, revealed that the only genes in the “superpathway of cholesterol biosynthesis” were Idi1 (upregulated) and Hmgcs2 (downregulated). The fraction of stretched myocytes expressing Nile red was significantly decreased by RNA interference of Idi1 (p < 0.05) and was significantly decreased by plasmid transfection of Hmgcs2 (p = 0.004). Conclusions: The Idi1 and Hmgcs2 genes have regulatory roles in atrial lipotoxic myopathy associated with atrial enlargement.

Original languageEnglish
Article number4094
JournalInternational Journal of Molecular Sciences
Volume19
Issue number12
DOIs
Publication statusPublished - Jan 1 2018

Fingerprint

muscle cells
genes
Muscle Cells
Genes
Cholesterol
cholesterol
Mitral Valve Insufficiency
metabolism
Muscular Diseases
Regulator Genes
Metabolism
Lipids
lipids
Down-Regulation
monocytes
lipoproteins
Lipoproteins
biosynthesis
plasmids
Biosynthesis

Keywords

  • Atrium
  • Genes
  • Lipid
  • Myopathy

ASJC Scopus subject areas

  • Catalysis
  • Molecular Biology
  • Spectroscopy
  • Computer Science Applications
  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

Cite this

Fang, C. Y., Chen, M. C., Chang, T. H., Wu, C. C., Chang, J. P., Huang, H. D., ... Lee, W. C. (2018). Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes. International Journal of Molecular Sciences, 19(12), [4094]. https://doi.org/10.3390/ijms19124094

Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes. / Fang, Chih Yuan; Chen, Mien Cheng; Chang, Tzu Hao; Wu, Chia Chen; Chang, Jen Ping; Huang, Hsien Da; Ho, Wan Chun; Wang, Yi Zhen; Pan, Kuo Li; Lin, Yu Sheng; Huang, Yao Kuang; Chen, Chien Jen; Lee, Wei Chieh.

In: International Journal of Molecular Sciences, Vol. 19, No. 12, 4094, 01.01.2018.

Research output: Contribution to journalArticle

Fang, CY, Chen, MC, Chang, TH, Wu, CC, Chang, JP, Huang, HD, Ho, WC, Wang, YZ, Pan, KL, Lin, YS, Huang, YK, Chen, CJ & Lee, WC 2018, 'Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes', International Journal of Molecular Sciences, vol. 19, no. 12, 4094. https://doi.org/10.3390/ijms19124094
Fang, Chih Yuan ; Chen, Mien Cheng ; Chang, Tzu Hao ; Wu, Chia Chen ; Chang, Jen Ping ; Huang, Hsien Da ; Ho, Wan Chun ; Wang, Yi Zhen ; Pan, Kuo Li ; Lin, Yu Sheng ; Huang, Yao Kuang ; Chen, Chien Jen ; Lee, Wei Chieh. / Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes. In: International Journal of Molecular Sciences. 2018 ; Vol. 19, No. 12.
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abstract = "Background: Lipid expression is increased in the atrial myocytes of mitral regurgitation (MR) patients. This study aimed to investigate key regulatory genes and mechanisms of atrial lipotoxic myopathy in MR. Methods: The HL-1 atrial myocytes were subjected to uniaxial cyclic stretching for eight hours. Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism were analyzed by PCR assay (168 genes). Results: The stretched myocytes had significantly larger cell size and higher lipid expression than non-stretched myocytes (all p < 0.001). Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism in the myocytes were analyzed by PCR assay (168 genes). In comparison with their counterparts in non-stretched myocytes, seven genes in stretched monocytes (Idi1, Olr1, Nr1h4, Fabp2, Prkag3, Slc27a5, Fabp6) revealed differential upregulation with an altered fold change >1.5. Nine genes in stretched monocytes (Apoa4, Hmgcs2, Apol8, Srebf1, Acsm4, Fabp1, Acox2, Acsl6, Gk) revealed differential downregulation with an altered fold change <0.67. Canonical pathway analysis, using Ingenuity Pathway Analysis software, revealed that the only genes in the “superpathway of cholesterol biosynthesis” were Idi1 (upregulated) and Hmgcs2 (downregulated). The fraction of stretched myocytes expressing Nile red was significantly decreased by RNA interference of Idi1 (p < 0.05) and was significantly decreased by plasmid transfection of Hmgcs2 (p = 0.004). Conclusions: The Idi1 and Hmgcs2 genes have regulatory roles in atrial lipotoxic myopathy associated with atrial enlargement.",
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T1 - Idi1 and Hmgcs2 are affected by stretch in HL-1 atrial myocytes

AU - Fang, Chih Yuan

AU - Chen, Mien Cheng

AU - Chang, Tzu Hao

AU - Wu, Chia Chen

AU - Chang, Jen Ping

AU - Huang, Hsien Da

AU - Ho, Wan Chun

AU - Wang, Yi Zhen

AU - Pan, Kuo Li

AU - Lin, Yu Sheng

AU - Huang, Yao Kuang

AU - Chen, Chien Jen

AU - Lee, Wei Chieh

PY - 2018/1/1

Y1 - 2018/1/1

N2 - Background: Lipid expression is increased in the atrial myocytes of mitral regurgitation (MR) patients. This study aimed to investigate key regulatory genes and mechanisms of atrial lipotoxic myopathy in MR. Methods: The HL-1 atrial myocytes were subjected to uniaxial cyclic stretching for eight hours. Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism were analyzed by PCR assay (168 genes). Results: The stretched myocytes had significantly larger cell size and higher lipid expression than non-stretched myocytes (all p < 0.001). Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism in the myocytes were analyzed by PCR assay (168 genes). In comparison with their counterparts in non-stretched myocytes, seven genes in stretched monocytes (Idi1, Olr1, Nr1h4, Fabp2, Prkag3, Slc27a5, Fabp6) revealed differential upregulation with an altered fold change >1.5. Nine genes in stretched monocytes (Apoa4, Hmgcs2, Apol8, Srebf1, Acsm4, Fabp1, Acox2, Acsl6, Gk) revealed differential downregulation with an altered fold change <0.67. Canonical pathway analysis, using Ingenuity Pathway Analysis software, revealed that the only genes in the “superpathway of cholesterol biosynthesis” were Idi1 (upregulated) and Hmgcs2 (downregulated). The fraction of stretched myocytes expressing Nile red was significantly decreased by RNA interference of Idi1 (p < 0.05) and was significantly decreased by plasmid transfection of Hmgcs2 (p = 0.004). Conclusions: The Idi1 and Hmgcs2 genes have regulatory roles in atrial lipotoxic myopathy associated with atrial enlargement.

AB - Background: Lipid expression is increased in the atrial myocytes of mitral regurgitation (MR) patients. This study aimed to investigate key regulatory genes and mechanisms of atrial lipotoxic myopathy in MR. Methods: The HL-1 atrial myocytes were subjected to uniaxial cyclic stretching for eight hours. Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism were analyzed by PCR assay (168 genes). Results: The stretched myocytes had significantly larger cell size and higher lipid expression than non-stretched myocytes (all p < 0.001). Fatty acid metabolism, lipoprotein signaling, and cholesterol metabolism in the myocytes were analyzed by PCR assay (168 genes). In comparison with their counterparts in non-stretched myocytes, seven genes in stretched monocytes (Idi1, Olr1, Nr1h4, Fabp2, Prkag3, Slc27a5, Fabp6) revealed differential upregulation with an altered fold change >1.5. Nine genes in stretched monocytes (Apoa4, Hmgcs2, Apol8, Srebf1, Acsm4, Fabp1, Acox2, Acsl6, Gk) revealed differential downregulation with an altered fold change <0.67. Canonical pathway analysis, using Ingenuity Pathway Analysis software, revealed that the only genes in the “superpathway of cholesterol biosynthesis” were Idi1 (upregulated) and Hmgcs2 (downregulated). The fraction of stretched myocytes expressing Nile red was significantly decreased by RNA interference of Idi1 (p < 0.05) and was significantly decreased by plasmid transfection of Hmgcs2 (p = 0.004). Conclusions: The Idi1 and Hmgcs2 genes have regulatory roles in atrial lipotoxic myopathy associated with atrial enlargement.

KW - Atrium

KW - Genes

KW - Lipid

KW - Myopathy

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