HAX1-Overexpression Augments Cardioprotective Efficacy of Stem Cell-Based Therapy Through Mediating Hippo-Yap Signaling

• Published in: Stem cell reviews and reports 2024-08, Vol.20 (6), p.1569-1586
• Main Authors: Cai, Wen-Feng, Jiang, Lin, Liang, Jialiang, Dutta, Suchandrima, Huang, Wei, He, Xingyu, Wu, Zhichao, Paul, Christian, Gao, Xiang, Xu, Meifeng, Kanisicak, Onur, Zheng, Junmeng, Wang, Yigang
• Format: Article
• Language: English
• Subjects: Angiogenesis; Ataxin; Biomedical and Life Sciences; Biomedical Engineering and Bioengineering; Cell Biology; Cell death; Cell proliferation; Cell survival; Cell therapy; Fibrosis; Growth factors; Heart; Hypoxia; Ischemia; Kinases; Life Sciences; Myocardial infarction; Nuclear transport; Phosphorylation; Progenitor cells; Protein transport; Protein X; Proteins; Regenerative Medicine/Tissue Engineering; Signal transduction; Stem Cells; Stromal cells; Transcription activation; Vascularization; Yes-associated protein
• ISSN: 2629-3269; 2629-3277; 2629-3277
• DOI: 10.1007/s12015-024-10729-z

Although stem/progenitor cell therapy shows potential for myocardial infarction repair, enhancing the therapeutic efficacy could be achieved through additional genetic modifications. HCLS1-associated protein X-1 (HAX1) has been identified as a versatile modulator responsible for cardio-protective signaling, while its role in regulating stem cell survival and functionality remains unknown. In this study, we investigated whether HAX1 can augment the protective potential of Sca1 + cardiac stromal cells (CSCs) for myocardial injury. The overexpression of HAX1 significantly increased cell proliferation and conferred enhanced resistance to hypoxia-induced cell death in CSCs. Mechanistically, HAX1 can interact with Mst1 (a prominent conductor of Hippo signal transduction) and inhibit its kinase activity for protein phosphorylation. This inhibition led to enhanced nuclear translocation of Yes-associated protein (YAP) and activation of downstream therapeutic-related genes. Notably, HAX1 overexpression significantly increased the pro-angiogenic potential of CSCs, as demonstrated by elevated expression of vascular endothelial growth factors. Importantly, implantation of HAX1-overexpressing CSCs promoted neovascularization, protected against functional deterioration, and ameliorated cardiac fibrosis in ischemic mouse hearts. In conclusion, HAX1 emerges as a valuable and efficient inducer for enhancing the effectiveness of cardiac stem or progenitor cell therapeutics. Graphical Abstract