Sheehy Sean P, Huang Sui, Parker Kevin Kit
Disease Biophysics Group, School of Engineering and Applied Sciences, Harvard University, 29 Oxford Street, Cambridge, MA 02138, USA.
Circ Cardiovasc Genet. 2009 Apr;2(2):116-24. doi: 10.1161/CIRCGENETICS.108.806935. Epub 2009 Feb 18.
Cardiac hypertrophy is classically regarded as a compensatory response, yet the active tissue remodeling processes triggered by various types of mechanical stress can enhance or diminish the function of the heart. Despite the disparity in outcomes, there are similarities in the hypertrophic responses. We hypothesized that a generic genetic response that is not dependent on the particular nature of the hypertrophic stimulus exists. To test our hypothesis, we compared the temporal evolution of transcriptomes measured in hearts subjected to either adaptive (exercise-induced) or maladaptive (aortic banding-induced) hypertrophy.
Generic hypertrophy-associated genes were identified and distinguished from stimulus-dependent transcripts by coupling a metric of cardiac growth with a dynamic time-warping algorithm to align transcriptome changes with respect to the hypertrophy response. The major differences in expression between the adaptive and maladaptive hypertrophy models were centered around the genes involved in metabolism, fibrosis, and immune response. Conversely, transcripts with common expression patterns in both hypertrophy models were associated with signal transduction, cytoskeletal development, and muscle contraction. Thus, despite the apparent differences in the expression response of the heart to either athletic conditioning or pressure overload, there is a set of genes that displays similar expression profiles.
This finding lends support to the notion of a generalized cardiac growth mechanism that is activated in response to mechanical perturbation. The common and unique genetic signatures of adaptive and maladaptive hypertrophy may be useful in the diagnosis and treatment of pathological myocardial remodeling.
心脏肥大传统上被视为一种代偿反应,然而,由各种类型的机械应力触发的活跃组织重塑过程可增强或削弱心脏功能。尽管结果存在差异,但肥大反应存在相似之处。我们假设存在一种不依赖于肥大刺激的特定性质的通用遗传反应。为了验证我们的假设,我们比较了在经历适应性(运动诱导)或适应性不良(主动脉缩窄诱导)肥大的心脏中测量的转录组的时间演变。
通过将心脏生长指标与动态时间规整算法相结合,以对齐转录组变化与肥大反应,从而识别出通用的肥大相关基因,并将其与刺激依赖性转录本区分开来。适应性和适应性不良肥大模型之间表达的主要差异集中在参与代谢、纤维化和免疫反应的基因上。相反,在两种肥大模型中具有共同表达模式的转录本与信号转导、细胞骨架发育和肌肉收缩相关。因此,尽管心脏对运动调节或压力过载的表达反应存在明显差异,但仍有一组基因显示出相似的表达谱。
这一发现支持了一种广义心脏生长机制的概念,该机制在机械扰动时被激活。适应性和适应性不良肥大的共同和独特基因特征可能有助于病理性心肌重塑的诊断和治疗。