Shyng S L, Salpeter M M
Department of Neurobiology and Behavior, Cornell University, Ithaca, New York 14853.
J Cell Biol. 1989 Feb;108(2):647-51. doi: 10.1083/jcb.108.2.647.
Many studies exist on the effect of denervation on the degradation of acetylcholine receptors (AChRs) at the vertebrate neuromuscular junction (nmj). These studies have described the behavior of either the total population of junctional receptors at different times after denervation, or of the receptors present at the time of denervation (referred to as original receptors). No experimental studies yet exist on the degradation rate of the receptors newly inserted into denervated junctions. In the previous studies, the original receptors of mouse sternomastoid muscles were found to retain the slow degradation (t 1/2) of approximately 8-10 d of innervated junctional receptors for up to 10 d after denervation before accelerating to a t 1/2 of approximately 3 d. The total junctional receptors, on the other hand, showed a progressive increase in degradation rate from a t 1/2 of 8-10 d to a t 1/2 of 1 d. To reconcile these earlier observations, the present study examines the degradation of new receptors inserted into the nmj after denervation. To avoid possible contamination of the data with postdenervation extrajunctional receptors, we used transmission electron microscope autoradiography to study only receptors located at the postjunctional fold of the nmj. We established that the new receptors inserted into denervated junctions have a t 1/2 of approximately 1 d, considerably faster than that of the original receptors and equivalent to that of postdenervation extrajunctional receptors. Both original and new receptors are interspersed at the top of the junctional folds. Thus, until all the original receptors are degraded, the postjunctional membrane contains two populations of AChRs that maintain a total steady-state site density but degrade at different rates. The progressive increase in turnover rate of total AChRs therefore reflects the combined rates of the original and new receptors, as earlier postulated by Levitt and Salpeter (1981).
关于去神经支配对脊椎动物神经肌肉接头(nmj)处乙酰胆碱受体(AChRs)降解的影响,已有许多研究。这些研究描述了去神经支配后不同时间点接头受体的总体行为,或者去神经支配时存在的受体(称为原始受体)的行为。目前尚无关于新插入去神经支配接头的受体降解速率的实验研究。在先前的研究中,发现小鼠胸锁乳突肌的原始受体在去神经支配后长达10天内,仍保持着与神经支配接头受体相似的约8 - 10天的缓慢降解半衰期(t 1/2),之后加速至约3天的t 1/2。另一方面,接头受体总数的降解速率则从8 - 10天的t 1/2逐渐增加至1天的t 1/2。为了协调这些早期观察结果,本研究考察了去神经支配后插入nmj的新受体的降解情况。为避免去神经支配后接头外受体可能对数据造成的污染,我们使用透射电子显微镜放射自显影技术,仅研究位于nmj接头后褶皱处的受体。我们确定,插入去神经支配接头的新受体的t 1/2约为1天,这比原始受体的降解速度快得多,且与去神经支配后接头外受体的降解速度相当。原始受体和新受体都散布在接头褶皱的顶部。因此,在所有原始受体降解之前,接头后膜含有两类AChRs,它们维持着总的稳态位点密度,但降解速率不同。因此,总AChRs周转率的逐渐增加反映了原始受体和新受体的综合速率,正如Levitt和Salpeter(1981年)早期所推测的那样。