Identification of Novel Gene Regulatory Networks for Dystrophin Protein in Vascular Smooth Muscle Cells by Single-Nuclear Transcriptome Analysis

• Published in: Cells (Basel, Switzerland) Vol. 12; no. 6; p. 892
• Main Authors: Shen, Yan, Kim, Il-Man, Tang, Yaoliang
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.03.2023; MDPI
• Subjects: and single nuclear RNA sequencing; Animals; Anions; Antibodies; Blood pressure; Cardiomyocytes; Care and treatment; Cations; Channel gating; Clustering; Congestive heart failure; Diagnosis; Duchenne muscular dystrophy; Duchenne's muscular dystrophy; Dystrophin; Dystrophin - metabolism; Gene expression; Gene Expression Profiling; Gene mutations; Gene Regulatory Networks; Genetic aspects; Genomes; Health aspects; Hypotension; KCNQ5; KCNQ5 protein; Laboratories; Medical examination; Metabolic pathways; Metabolism; Mice; Mice, Inbred mdx; Muscle, Smooth, Vascular; Muscular dystrophy; Muscular Dystrophy, Duchenne - metabolism; Muscular Dystrophy, Duchenne - pathology; Musculoskeletal system; Mutation; Nonsense mutation; Ontology; Potassium; Potassium channels (voltage-gated); Proteins; Pyruvic acid; RNA, Small Nuclear; Ryanodine receptors; Skeletal muscle; Smooth muscle; snRNA; Therapeutic applications; Transcriptomes; Vascular smooth muscle; United States; United States > US; blood pressure; and single nuclear RNA sequencing; KCNQ5; dystrophin; Duchenne muscular dystrophy
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12060892

Duchenne muscular dystrophy is an X-linked recessive disease caused by mutations in dystrophin proteins that lead to heart failure and respiratory failure. Dystrophin ( ) is not only expressed in cardiomyocytes and skeletal muscle cells, but also in vascular smooth muscle cells (VSMCs). Patients with DMD have been reported to have hypotension. Single nuclear RNA sequencing (snRNA-seq) is a state-of-the-art technology capable of identifying niche-specific gene programs of tissue-specific cell subpopulations. To determine whether mutation alters blood pressure, we compared systolic, diastolic, and mean blood pressure levels in mdx mice (a mouse model of DMD carrying a nonsense mutation in gene) and the wide-type control mice. We found that mdx mice showed significantly lower systolic, diastolic, and mean blood pressure than control mice. To understand how mutation changes gene expression profiles from VSMCs, we analyzed an snRNA-seq dataset from the muscle nucleus of mutant ( ) mice and control (Ctrl) mice. Gene Ontology (GO) enrichment analysis revealed that the most significantly activated pathways in -VSMCs are involved in ion channel function (potassium channel activity, cation channel complex, and cation channel activity). Notably, we discovered that the -VSMCs showed significantly upregulated expression of KCNQ5 and RYR2, whereas the most suppressed pathways were transmembrane transporter activity (such as anion transmembrane transporter activity, inorganic anion transmembrane transporter activity, import into cell, and import across plasma membrane). Moreover, we analyzed metabolic pathways from the Kyoto Encyclopedia of Genes and Genomes (KEGG) using "scMetabolism" R package. -VSMCs exhibited dysregulation of pyruvate metabolism and nuclear acid metabolism. In conclusion, via the application of snRNA-seq, we (for the first time) identify the potential molecular regulation by in the upregulation of the expression of KCNQ5 genes in VSMCs, which helps us to understand the mechanism of hypotension in DMD patients. Our study potentially offers new possibilities for therapeutic interventions in systemic hypotension in DMD patients with pharmacological inhibition of KCNQ5.