Age-Related Decline in NCKX4-Mediated Calcium Clearance Accelerates Aortic Remodeling and Drives Early Vascular Aging

NCKX4介导的钙清除率随年龄增长而下降,加速主动脉重塑并导致血管早期老化

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Abstract

Aging is the primary nonmodifiable risk factor for cardiovascular diseases (CVDs), with older women facing a greater risk of CVDs than age-matched men. Vascular smooth muscle cells (VSMCs) dysfunction and impaired calcium (Ca (2+) ) handling are recognized as central contributors to arterial stiffening and calcification. However, the molecular and functional determinants of Ca (2+) clearance in vascular aging remains a topic of ongoing research. We identify the ( N a (+) )-sodium/ C a (2+) -calcium ( K (+) )-potassium-dependent e x changer 4 ( NCKX4 ) as a critical functional regulator of VSMCs Ca²⁺ clearance and vascular integrity. We demonstrate that NCKX4 (coded by Slc24A4 ) expression is markedly reduced in aorta of aged (72-78 weeks) mice, with a pronounced decline in females. Functional assays revealed impaired Ca (2+) clearance in both aged and Nckx4 (⁻) (/) (⁻) VSMCs, which was accompanied by increased calcification. Histomorphometric analyses of young Nckx4 (⁻) (/) (⁻) mice revealed fragmentation of elastic fibers, collagen accumulation, wall thickening, and extracellular matrix (ECM) remodeling, all hallmarks of vascular aging that closely resembled those of aged wild-type mice. Transcriptomic profiling of VSMCs showed that loss of NCKX4 alters pathways linked to Ca (2+) -integrin signaling, ECM turnover, and mineralization, including dysregulation of protective anchorage integrins, microfibril-stabilizing, osteogenic drivers and pro-fibrotic integrins. These findings support a model in which impaired Ca (2+) clearance promotes maladaptive inside-out integrin signaling, disrupting VSMCs anchorage, ECM homeostasis, and mineralization processes. Collectively, our results establish NCKX4 as a previously unrecognized determinant of vascular aging, whose decline accelerates premature arterial remodeling and calcification. This study positions NCKX4 as a potential mechanistic link between age, sex-dependent vulnerability, and vascular stiffening, with implications for novel therapeutic strategies targeting Ca (2+) handling in CVDs prevention.

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