Russell S D, Cambon N, Nadal-Ginard B, Whalen R G
Département de Biologie Moléculaire, Institut Pasteur, Paris, France.
J Biol Chem. 1988 May 5;263(13):6370-4.
The appearance of the mRNA for the adult fast IIB myosin heavy chain (MHC) was examined during postnatal development of rats using an S1 nuclease assay. In normal rats, a large increase in the adult MHC mRNA began at 6-7 days after birth, whereas daily injections of newborn rats with 3 micrograms of triiodothyronine (T3) resulted in a precocious increase of the mRNA as early as 3 days after birth. Injection of a range of doses of T3 demonstrated that a large effect was obtained between 30 and 300 ng of T3/day/rat. Fast myosin protein was also precociously induced over the same range of T3 doses. This effect was also seen in denervated muscles, and muscles responded similarly to the different doses of T3 whether they were denervated or not. These results suggest that either thyroid hormone or some circulating factors induced by thyroid hormone are limiting factors in controlling the neonatal-to-adult fast MHC transition and that these factors may act directly on muscle tissue.
使用S1核酸酶分析法,在大鼠出生后的发育过程中检测了成年快速IIB型肌球蛋白重链(MHC)mRNA的出现情况。在正常大鼠中,成年MHC mRNA在出生后6 - 7天开始大幅增加,而每天给新生大鼠注射3微克三碘甲状腺原氨酸(T3)则导致mRNA早在出生后3天就出现早熟增加。注射一系列剂量的T3表明,在30至300 ng T3/天/大鼠的范围内可获得显著效果。快速肌球蛋白蛋白也在相同的T3剂量范围内被早熟诱导。在去神经支配的肌肉中也观察到了这种效应,并且无论肌肉是否去神经支配,它们对不同剂量T3的反应相似。这些结果表明,甲状腺激素或甲状腺激素诱导的某些循环因子是控制新生儿到成年快速MHC转变的限制因素,并且这些因素可能直接作用于肌肉组织。