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Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction.

Publication ,  Journal Article
Gao, C; Howard-Quijano, K; Rau, C; Takamiya, T; Song, Y; Shivkumar, K; Wang, Y; Mahajan, A
Published in: PLoS One
2017

BACKGROUND: Chronic myocardial infarction (MI) triggers pathological remodeling in the heart and cardiac nervous system. Abnormal function of the autonomic nervous system (ANS), including stellate ganglia (SG) and dorsal root ganglia (DRG) contribute to increased sympathoexcitation, cardiac dysfunction and arrythmogenesis. ANS modulation is a therapeutic target for arrhythmia associated with cardiac injury. However, the molecular mechanism involved in the pathological remodeling in ANS following cardiac injury remains to be established. METHODS AND RESULTS: In this study, we performed transcriptome analysis by RNA-sequencing in thoracic SG and (T1-T4) DRG obtained from Yorkshire pigs following either acute (3 to 5 hours) or chronic (8 weeks) myocardial infarction. By differential expression and weighted gene co-expression network analysis (WGCNA), we identified significant transcriptome changes and specific gene modules in the ANS tissues in response to myocardial infarction at either acute or chronic phases. Both differential expressed genes and the member genes of the WGCNA gene module associated with post-infarct condition were significantly enriched for inflammatory signaling and apoptotic cell death. Targeted validation analysis supported a significant induction of inflammatory and apoptotic signal in both SG and DRG following myocardial infarction, along with cellular evidence of apoptosis induction based on TUNEL analysis. Importantly, these molecular changes were observed specifically in the thoracic segments but not in their counterparts obtained from lumbar sections. CONCLUSION: Myocardial injury leads to time-dependent global changes in gene expression in the innervating ANS. Induction of inflammatory gene expression and loss of neuron cell viability in SG and DRG are potential novel mechanisms contributing to abnormal ANS function which can promote cardiac arrhythmia and pathological remodeling in myocardium.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2017

Volume

12

Issue

5

Start / End Page

e0177750

Location

United States

Related Subject Headings

  • Swine
  • Stellate Ganglion
  • Myocardial Infarction
  • Male
  • Inflammation
  • General Science & Technology
  • Gene Expression Profiling
  • Ganglia, Spinal
  • Apoptosis
  • Animals
 

Citation

APA
Chicago
ICMJE
MLA
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Gao, C., Howard-Quijano, K., Rau, C., Takamiya, T., Song, Y., Shivkumar, K., … Mahajan, A. (2017). Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction. PLoS One, 12(5), e0177750. https://doi.org/10.1371/journal.pone.0177750
Gao, Chen, Kimberly Howard-Quijano, Christoph Rau, Tatsuo Takamiya, Yang Song, Kalyanam Shivkumar, Yibin Wang, and Aman Mahajan. “Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction.PLoS One 12, no. 5 (2017): e0177750. https://doi.org/10.1371/journal.pone.0177750.
Gao C, Howard-Quijano K, Rau C, Takamiya T, Song Y, Shivkumar K, et al. Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction. PLoS One. 2017;12(5):e0177750.
Gao, Chen, et al. “Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction.PLoS One, vol. 12, no. 5, 2017, p. e0177750. Pubmed, doi:10.1371/journal.pone.0177750.
Gao C, Howard-Quijano K, Rau C, Takamiya T, Song Y, Shivkumar K, Wang Y, Mahajan A. Inflammatory and apoptotic remodeling in autonomic nervous system following myocardial infarction. PLoS One. 2017;12(5):e0177750.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2017

Volume

12

Issue

5

Start / End Page

e0177750

Location

United States

Related Subject Headings

  • Swine
  • Stellate Ganglion
  • Myocardial Infarction
  • Male
  • Inflammation
  • General Science & Technology
  • Gene Expression Profiling
  • Ganglia, Spinal
  • Apoptosis
  • Animals