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Decoding JMJD proteins in cardiovascular and cerebrovascular diseases: From structure to function
Guangzhi Hao1, Yiyang Chen2, Yong Liang1
1Department of Neurosurgery, The General Hospital of Northern Theater Command, No. 83, Wenhua Road, Shenhe District, Shenyang, Liaoning 110016, China.
Insights
Jumonji C domain-containing (JMJD) proteins are key epigenetic regulators influencing cardiovascular and cerebrovascular diseases. Understanding their roles offers potential for new therapeutic strategies targeting these widespread conditions.
Area of Science:
- Biochemistry
- Epigenetics
- Molecular Biology
Background:
- Cardiovascular and cerebrovascular diseases are leading global causes of mortality and disability.
- Epigenetic modifications, influenced by environmental factors, play a crucial role in disease susceptibility.
- The Jumonji C domain-containing (JMJD) protein family acts as critical histone demethylases in epigenetic regulation.
Purpose of the Study:
- To review the structural characteristics of JMJD family members.
- To highlight the roles of JMJD proteins in cardiovascular and cerebrovascular disorders.
- To explore potential pharmacological strategies targeting JMJD proteins.
Main Methods:
- Literature review of recent studies on JMJD proteins.
- Analysis of structural features of JMJD family members.
- Synthesis of findings on JMJD protein involvement in disease pathology.
Main Results:
- JMJD proteins are identified as pivotal epigenetic regulators in cardiac hypertrophy, atherosclerosis, myocardial ischemia-reperfusion injury, and ischemic stroke.
- These proteins are implicated in pathological processes including oxidative stress, macrophage polarization, mitochondrial autophagy, and apoptosis.
- The review details the involvement of specific JMJD proteins in disease mechanisms.
Conclusions:
- JMJD proteins are critical epigenetic modulators in cardiovascular and cerebrovascular diseases.
- Elucidating JMJD protein functions provides insights into disease pathogenesis.
- Targeting JMJD proteins may offer novel therapeutic avenues for treating these conditions.
Abstract:
Cardiovascular and cerebrovascular diseases remain major causes of death and disability worldwide. Their susceptibility is closely linked to epigenetic modifications triggered by environmental factors. The Jumonji C domain-containing (JMJD) protein family consists of Fe²⁺- and 2-oxoglutarate (2OG)-dependent oxidases that primarily mediate histone demethylation or hydroxylation of specific amino acid residues, functioning as critical histone demethylases in epigenetic regulation. Recent studies have identified JMJD proteins as pivotal epigenetic regulators in various cardiovascular and cerebrovascular diseases, including cardiac hypertrophy (CH), atherosclerosis (AS), myocardial ischemia-reperfusion injury (MIRI), and ischemic stroke (IS). These proteins are deeply involved in pathological processes such as oxidative stress, macrophage polarization, mitochondrial autophagy, and apoptosis. Accordingly, elucidating the functions of JMJD proteins has gained increasing attention. This review summarizes the structural characteristics of JMJD family members and highlights their roles in cardiovascular and cerebrovascular disorders. These insights may help guide future pharmacological strategies targeting JMJD proteins.
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