Department of Human Genetics (K.R., C.B.W.), University of California.
Department of Medicine (K.R.), University of California.
Circ Res. 2022 Jun 10;130(12):1747-1762. doi: 10.1161/CIRCRESAHA.122.320259. Epub 2022 Jun 9.
Sex is a key risk factor for many types of cardiovascular disease. It is imperative to understand the mechanisms underlying sex differences to devise optimal preventive and therapeutic approaches for all individuals. Both biological sex (determined by sex chromosomes and gonadal hormones) and gender (social and cultural behaviors associated with femininity or masculinity) influence differences between men and women in disease susceptibility and pathology. Here, we focus on the application of experimental mouse models that elucidate the influence of 2 components of biological sex-sex chromosome complement (XX or XY) and gonad type (ovaries or testes). These models have revealed that in addition to well-known effects of gonadal hormones, sex chromosome complement influences cardiovascular risk factors, such as plasma cholesterol levels and adiposity, as well as the development of atherosclerosis and pulmonary hypertension. One mechanism by which sex chromosome dosage influences cardiometabolic traits is through sex-biased expression of X chromosome genes that escape X inactivation. These include chromatin-modifying enzymes that regulate gene expression throughout the genome. The identification of factors that determine sex-biased gene expression and cardiometabolic traits will expand our mechanistic understanding of cardiovascular disease processes and provide insight into sex differences that remain throughout the lifespan as gonadal hormone levels alter with age.
性别是许多类型心血管疾病的一个关键风险因素。了解性别差异的潜在机制对于为所有个体设计最佳的预防和治疗方法至关重要。生物学性别(由性染色体和性腺激素决定)和性别(与女性气质或男性气质相关的社会和文化行为)都影响着疾病易感性和病理方面男性和女性之间的差异。在这里,我们重点介绍了实验小鼠模型的应用,这些模型阐明了生物学性别两个组成部分(XX 或 XY 性染色体组成和卵巢或睾丸类型)对心血管风险因素的影响。这些模型表明,除了性腺激素的已知影响外,性染色体组成还会影响心血管风险因素,如血浆胆固醇水平和肥胖,以及动脉粥样硬化和肺动脉高压的发展。性染色体剂量影响心脏代谢特征的一种机制是通过逃避 X 染色体失活的 X 染色体基因的性别偏性表达。这些包括调节整个基因组基因表达的染色质修饰酶。确定决定性别偏性基因表达和心脏代谢特征的因素将扩展我们对心血管疾病过程的机制理解,并深入了解随着年龄的增长,随着性腺激素水平的变化,贯穿整个生命周期的性别差异。