Cation-dependent Mannose 6-Phosphate Receptor Functions as a Key Regulator of Palmitic Acid-induced Cell Death in Cardiomyocytes
*Corresponding Author:Received Date: Oct 01, 2023 / Published Date: Oct 30, 2023
Copyright: © 2023 . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Background: Palmitic acid (PA), a common saturated free fatty acid, is known as inducer of apoptosis in numerous cell types. M6PR-CD has been reported as a potential pro-apoptotic factor in several models. Objective: We aim to identify the critical regulatory molecules in the process of palmitate-induced apoptosis in H9C2 cardiomyocytes. Methods: Cells treated with 250 μM PA for 24 hours were collected. Transcriptome sequencing and bioinformatics analysis were carried out to screen the differentially expressed genes. RT-PCR and western blot were used to confirm the up-regulation of M6PR-CD. The function of M6PR-CD was studied through the detection of cell viability, apoptosis and intracellular ROS levels. Results: A total of 1025 differentially expressed genes were screened by transcriptome sequencing, including 718 up-regulated genes and 307 down-regulated genes. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis were mainly focused on the apoptotic and stress. M6PR-CD was significantly upregulated with PA treatment. Knockdown of M6PR-CD alleviated the PA-induced apoptosis with lower ROS levels. After transfection with M6PR-CD siRNA, it was also found that compensatory increase in M6PR-CI subtype did not exist, and the expression of caspase-3 was almost the same. Conclusion: This study identified a number of genes related to PA-induced cardiomyocytes apoptosis through transcriptome sequencing. It was clarified for the first time that M6PR-CD could induce H9C2 cardiomyocytes apoptosis by enhancing ROS production rather than being Caspase-3-dependent, providing a theoretic basis for us to have a better understanding of the intrinsic mechanism.