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本文引用的文献

1
Growth-inhibiting conditions slow growth plate senescence.抑制生长的条件可减缓生长板衰老。
J Endocrinol. 2011 Jan;208(1):59-67. doi: 10.1677/JOE-10-0302. Epub 2010 Oct 25.
2
Connecting serum IGF-1, body size, and age in the domestic dog.家犬血清胰岛素样生长因子-1、体型与年龄之间的联系。
Age (Dordr). 2011 Sep;33(3):475-83. doi: 10.1007/s11357-010-9182-4. Epub 2010 Sep 24.
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Regulation of muscle mass by follistatin and activins.卵泡抑素和激活素对肌肉量的调节
Mol Endocrinol. 2010 Oct;24(10):1998-2008. doi: 10.1210/me.2010-0127. Epub 2010 Sep 1.
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Russell-Silver syndrome.Russell-Silver 综合征。
Am J Med Genet C Semin Med Genet. 2010 Aug 15;154C(3):355-64. doi: 10.1002/ajmg.c.30274.
5
The Merlin/NF2 tumor suppressor functions through the YAP oncoprotein to regulate tissue homeostasis in mammals.梅林/NF2 肿瘤抑制因子通过 YAP 癌蛋白在哺乳动物中调节组织内稳态。
Dev Cell. 2010 Jul 20;19(1):27-38. doi: 10.1016/j.devcel.2010.06.015.
6
In vitro measurement of post-natal changes in proliferating satellite cell frequency during rat muscle growth.在体测量大鼠肌肉生长过程中增殖卫星细胞频率的出生后变化。
Anim Sci J. 2010 Apr;81(2):245-51. doi: 10.1111/j.1740-0929.2009.00734.x.
7
The mTOR pathway: a new target in cancer therapy.mTOR 通路:癌症治疗的新靶点。
Curr Cancer Drug Targets. 2010 Aug;10(5):484-95. doi: 10.2174/156800910791517172.
8
Coordinated postnatal down-regulation of multiple growth-promoting genes: evidence for a genetic program limiting organ growth.协调产后多种促生长基因的下调:限制器官生长的遗传程序的证据。
FASEB J. 2010 Aug;24(8):3083-92. doi: 10.1096/fj.09-152835. Epub 2010 Apr 6.
9
Follistatin gene delivery enhances muscle growth and strength in nonhuman primates.卵泡抑素基因递送增强了非人灵长类动物的肌肉生长和力量。
Sci Transl Med. 2009 Nov 11;1(6):6ra15. doi: 10.1126/scitranslmed.3000112.
10
Comparison of gene expression in hepatocellular carcinoma, liver development, and liver regeneration.肝细胞癌、肝发育和肝再生中基因表达的比较。
Mol Genet Genomics. 2010 May;283(5):485-92. doi: 10.1007/s00438-010-0530-y. Epub 2010 Apr 1.

哺乳动物身体生长受限的机制。

Mechanisms limiting body growth in mammals.

机构信息

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.

出版信息

Endocr Rev. 2011 Jun;32(3):422-40. doi: 10.1210/er.2011-0001. Epub 2011 Mar 25.

DOI:10.1210/er.2011-0001
PMID:21441345
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3365796/
Abstract

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.

摘要

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。