Rios Coronado Pamela E, Zhou Jiayan, Fan Xiaochen, Zanetti Daniela, Naftaly Jeffrey A, Prabala Pratima, Martínez Jaimes Azalia M, Farah Elie N, Kundu Soumya, Deshpande Salil S, Evergreen Ivy, Kho Pik Fang, Ma Qixuan, Hilliard Austin T, Abramowitz Sarah, Pyarajan Saiju, Dochtermann Daniel, Damrauer Scott M, Chang Kyong-Mi, Levin Michael G, Winn Virginia D, Paşca Anca M, Plomondon Mary E, Waldo Stephen W, Tsao Philip S, Kundaje Anshul, Chi Neil C, Clarke Shoa L, Red-Horse Kristy, Assimes Themistocles L
Department of Biology, Stanford University, Stanford, CA, USA.
Department of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA; VA Palo Alto Health Care System, Palo Alto, CA, USA.
Cell. 2025 Apr 3;188(7):1784-1806.e22. doi: 10.1016/j.cell.2025.02.005. Epub 2025 Mar 5.
Coronary arteries have a specific branching pattern crucial for oxygenating heart muscle. Among humans, there is natural variation in coronary anatomy with respect to perfusion of the inferior/posterior left heart, which can branch from either the right arterial tree, the left, or both-a phenotype known as coronary dominance. Using angiographic data for >60,000 US veterans of diverse ancestry, we conducted a genome-wide association study of coronary dominance, revealing moderate heritability and identifying ten significant loci. The strongest association occurred near CXCL12 in both European- and African-ancestry cohorts, with downstream analyses implicating effects on CXCL12 expression. We show that CXCL12 is expressed in human fetal hearts at the time dominance is established. Reducing Cxcl12 in mice altered coronary dominance and caused septal arteries to develop away from Cxcl12 expression domains. These findings indicate that CXCL12 patterns human coronary arteries, paving the way for "medical revascularization" through targeting developmental pathways.
冠状动脉具有特定的分支模式,这对于为心肌提供氧气至关重要。在人类中,冠状动脉解剖结构在为左心室下壁/后壁供血方面存在自然变异,其供血分支可以来自右冠状动脉系统、左冠状动脉系统,或者两者皆有——这种表型被称为冠状动脉优势。利用超过60000名不同血统的美国退伍军人的血管造影数据,我们进行了一项关于冠状动脉优势的全基因组关联研究,揭示了适度的遗传力并确定了10个显著位点。在欧洲和非洲血统队列中,最强的关联出现在CXCL12附近,下游分析表明其对CXCL12表达有影响。我们发现CXCL12在人类胎儿心脏确立优势时表达。在小鼠中减少Cxcl12会改变冠状动脉优势,并导致间隔动脉远离Cxcl12表达域发育。这些发现表明CXCL12塑造了人类冠状动脉,为通过靶向发育途径进行“医学血管再生”铺平了道路。