Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, Torrance, California.
Am J Physiol Cell Physiol. 2013 Oct 1;305(7):C682-9. doi: 10.1152/ajpcell.00197.2013. Epub 2013 Jul 24.
I hypothesize that the First Principles of Physiology (FPPs) were co-opted during the vertebrate transition from water to land, beginning with the acquisition of cholesterol by eukaryotes, facilitating unicellular evolution over the course of the first 4.5 billion years of the Earth's history, in service to the reduction in intracellular entropy, far from equilibrium. That mechanism was perpetuated by the advent of cholesterol in the cell membrane of unicellular eukaryotes, ultimately giving rise to the metazoan homologs of the gut, lung, kidney, skin, bone, and brain. Parathyroid hormone-related protein (PTHrP), whose cognate receptor underwent a gene duplication during the transition from fish to amphibians, facilitated gas exchange for the water-to-land transition, since PTHrP is necessary for the formation of lung alveoli: deletion of the PTHrP gene in mice causes the offspring to die within a few minutes of birth due to the absence of alveoli. Moreover, PTHrP is central to the development and homeostasis of the kidney, skin, gut, bone, and brain. Therefore, duplication of the PTHrP receptor gene is predicted to have facilitated the molecular evolution of all the necessary traits for land habitation through a common cellular and molecular motif. Subsequent duplication of the β-adrenergic receptor gene permitted blood pressure control within the lung microvasculature, allowing further evolution of the lung by increasing its surface area. I propose that such gene duplications were the result of shear stress on the microvasculature, locally generating radical oxygen species that caused DNA mutations, giving rise to duplication of the PTHrP and β-adrenergic receptor genes. I propose that one can determine the FPPs by systematically tracing the molecular homologies between the lung, skin, kidney, gut, bone, and brain across development, phylogeny, and pathophysiology as a type of "reverse evolution." By tracing such relationships back to unicellular organisms, one can use the underlying principles to predict homeostatic failure as disease, thereby also potentially forming the basis for maneuvers that can treat or even prevent such failure.
我假设生理学基本原理(FPPs)在脊椎动物从水中到陆地的过渡中被共同采用,最初是真核生物获得胆固醇,促进了单细胞在地球历史的前 45 亿年中的进化,服务于远离平衡的细胞内熵的减少。这种机制通过胆固醇在单细胞真核生物的细胞膜中的出现而得以延续,最终导致了肠道、肺、肾、皮肤、骨骼和大脑的后生动物同源物的出现。甲状旁腺激素相关蛋白(PTHrP)的同源受体在鱼类到两栖动物的过渡中发生了基因复制,促进了从水中到陆地的过渡中的气体交换,因为 PTHrP 是肺肺泡形成所必需的:在老鼠中删除 PTHrP 基因会导致后代在出生后的几分钟内死亡,因为缺乏肺泡。此外,PTHrP 是肾脏、皮肤、肠道、骨骼和大脑的发育和稳态的核心。因此,PTHrP 受体基因的复制预计通过一个共同的细胞和分子主题促进了所有适应陆地生活所需特征的分子进化。β-肾上腺素能受体基因的随后复制允许在肺微血管中控制血压,通过增加其表面积进一步促进肺的进化。我提出,这种基因复制是微血管上的剪切应力的结果,局部产生自由基氧物质,导致 DNA 突变,导致 PTHrP 和 β-肾上腺素能受体基因的复制。我提出,可以通过系统地追踪肺、皮肤、肾脏、肠道、骨骼和大脑在发育、系统发育和病理生理学之间的分子同源性来确定 FPPs,作为一种“反向进化”。通过将这些关系追溯到单细胞生物,可以利用潜在的原则来预测稳态衰竭作为疾病,从而也有可能形成可以治疗甚至预防这种衰竭的操作的基础。