Program in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892, USA.
Endocr Rev. 2011 Jun;32(3):422-40. doi: 10.1210/er.2011-0001. Epub 2011 Mar 25.
Recent studies have begun to provide insight into a long-standing mystery in biology-why body growth in animals is rapid in early life but then progressively slows, thus imposing a limit on adult body size. This growth deceleration in mammals is caused by potent suppression of cell proliferation in multiple tissues and is driven primarily by local, rather than systemic, mechanisms. Recent evidence suggests that this progressive decline in proliferation results from a genetic program that occurs in multiple organs and involves the down-regulation of a large set of growth-promoting genes. This program does not appear to be driven simply by time, but rather depends on growth itself, suggesting that the limit on adult body size is imposed by a negative feedback loop. Different organs appear to use different types of information to precisely target their adult size. For example, skeletal and cardiac muscle growth are negatively regulated by myostatin, the concentration of which depends on muscle mass itself. Liver growth appears to be modulated by bile acid flux, a parameter that reflects organ function. In pancreas, organ size appears to be limited by the initial number of progenitor cells, suggesting a mechanism based on cell-cycle counting. Further elucidation of the fundamental mechanisms suppressing juvenile growth is likely to yield important insights into the pathophysiology of childhood growth disorders and of the unrestrained growth of cancer. In addition, improved understanding of these growth-suppressing mechanisms may someday allow their therapeutic suspension in adult tissues to facilitate tissue regeneration.
最近的研究开始深入揭示生物学中的一个长期谜团——为什么动物在生命早期的身体生长迅速,但随后逐渐减缓,从而限制了成年后的身体大小。这种哺乳动物的生长减速是由多种组织中细胞增殖的强烈抑制引起的,主要是由局部而不是全身机制驱动的。最近的证据表明,这种增殖的逐渐下降是由一个在多个器官中发生的遗传程序引起的,涉及到大量促进生长的基因的下调。这个程序似乎不是简单地由时间驱动的,而是依赖于生长本身,这表明成年身体大小的限制是由负反馈回路引起的。不同的器官似乎使用不同类型的信息来精确地确定其成年大小。例如,骨骼和心肌的生长受到肌肉生长抑制素(myostatin)的负调控,其浓度取决于肌肉质量本身。肝生长似乎受到胆汁酸通量的调节,这是一个反映器官功能的参数。在胰腺中,器官大小似乎受到祖细胞初始数量的限制,这表明存在一种基于细胞周期计数的机制。进一步阐明抑制青少年生长的基本机制,可能会深入了解儿童生长障碍和癌症不受控制生长的病理生理学。此外,对这些生长抑制机制的更好理解,有朝一日可能会允许在成人组织中暂停这些机制,以促进组织再生。