Jiang Xiaogang, Edstrom Erik, Altun Mikael, Ulfhake Brun
Experimental Neurogerontology, Department of Neuroscience, Retzius Laboratory, Karolinska Institutet, 171 77 Stockholm, Sweden.
Aging Cell. 2003 Feb;2(1):47-57. doi: 10.1046/j.1474-9728.2003.00030.x.
The Shc family of proteins participates in mitogenic and survival signalling through binding to receptor tyrosine kinases. We report here on the expression of Shc in forebrain, spinal cord and hind limb muscles from 30-month-old rats with different degrees of sensorimotor impairment. ShcA (mRNA and protein) is up-regulated in skeletal muscles and spinal cord of aged rats, and this change relates to biological age, i.e. degree of behavioural incapacitation, rather than to chronological age. Western blot and RT-PCR revealed that the increase in ShcA selectively affected the p46 isoform in the spinal cord, whereas in muscle tissue a robust increase of p66(ShcA) was also evident. Furthermore, in parallel with the up-regulation of ShcA, an increase of p75(NTR) mRNA in the aged animals was observed. ShcB mRNA showed a tendency for down-regulation in both spinal cord and skeletal muscles, whereas the expression of ShcC was unaltered. Our data show that the regulation of Shc mRNAs in senescence is region as well as isoform specific. The regulatory changes may reflect changes in mitogenic/survival signalling induced by age-related cell and tissue damage. The coup-regulation of p66(ShcA) and p75(NTR) is interesting since both molecules have been associated with apoptosis.
Shc蛋白家族通过与受体酪氨酸激酶结合参与有丝分裂和存活信号传导。我们在此报告Shc在30月龄不同程度感觉运动功能受损大鼠的前脑、脊髓和后肢肌肉中的表达情况。ShcA(mRNA和蛋白)在老年大鼠的骨骼肌和脊髓中上调,且这种变化与生物学年龄相关,即行为失能程度,而非实际年龄。蛋白质印迹法和逆转录聚合酶链反应显示,ShcA的增加选择性地影响脊髓中的p46亚型,而在肌肉组织中p66(ShcA)也明显大量增加。此外,与ShcA的上调同时,在老年动物中观察到p75(NTR) mRNA增加。ShcB mRNA在脊髓和骨骼肌中均有下调趋势,而ShcC的表达未改变。我们的数据表明,衰老过程中Shc mRNA的调节具有区域和亚型特异性。这些调节变化可能反映了与年龄相关的细胞和组织损伤诱导的有丝分裂/存活信号传导的变化。p66(ShcA)和p75(NTR)的协同调节很有意思,因为这两种分子都与细胞凋亡有关。