Marino Rose, Hegde Anita, Barnes Kevin M, Schrier Lenneke, Emons Joyce A, Nilsson Ola, Baron Jeffrey
Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, National Institute of Child Health and Human Development, Bethesda, MD 20892-1103, USA.
Endocrinology. 2008 Apr;149(4):1820-8. doi: 10.1210/en.2007-0993. Epub 2008 Jan 3.
Catch-up growth is defined as a linear growth rate greater than expected for age after a period of growth inhibition. We hypothesized that catch-up growth occurs because growth-inhibiting conditions conserve the limited proliferative capacity of growth plate chondrocytes, thus slowing the normal process of growth plate senescence. When the growth-inhibiting condition resolves, the growth plates are less senescent and therefore grow more rapidly than normal for age. To test this hypothesis, we administered propylthiouracil to newborn rats for 8 wk to induce hypothyroidism and then stopped the propylthiouracil to allow catch-up growth. In untreated controls, the growth plates underwent progressive, senescent changes in multiple functional and structural characteristics. We also identified genes that showed large changes in mRNA expression in growth plate and used these changes as molecular markers of senescence. In treated animals, after stopping propylthiouracil, these functional, structural, and molecular senescent changes were delayed, compared with controls. This delayed senescence included a delayed decline in longitudinal growth rate, resulting in catch-up growth. The findings demonstrate that growth inhibition due to hypothyroidism slows the developmental program of growth plate senescence, including the normal decline in the rate of longitudinal bone growth, thus accounting for catch-up growth.
追赶生长被定义为在一段生长抑制期后,线性生长速率高于同年龄预期水平。我们推测,追赶生长的发生是因为生长抑制条件保存了生长板软骨细胞有限的增殖能力,从而减缓了生长板衰老的正常进程。当生长抑制条件解除时,生长板的衰老程度较低,因此比同年龄的正常情况生长得更快。为了验证这一假设,我们给新生大鼠服用丙硫氧嘧啶8周以诱导甲状腺功能减退,然后停止服用丙硫氧嘧啶以实现追赶生长。在未治疗的对照组中,生长板在多个功能和结构特征方面经历了渐进性的衰老变化。我们还鉴定了在生长板中mRNA表达有大幅变化的基因,并将这些变化用作衰老的分子标记。在治疗的动物中,停止服用丙硫氧嘧啶后,与对照组相比,这些功能、结构和分子水平的衰老变化出现延迟。这种衰老延迟包括纵向生长速率下降的延迟,从而导致追赶生长。这些发现表明,甲状腺功能减退引起的生长抑制减缓了生长板衰老的发育进程,包括纵向骨生长速率的正常下降,从而解释了追赶生长现象。