Mavrakis Manos, Lippincott-Schwartz Jennifer, Stratakis Constantine A, Bossis Ioannis
Cell Biology and Metabolism Branch, Section on Endocrinology and Genetics, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-5430, USA.
Autophagy. 2007 Mar-Apr;3(2):151-3. doi: 10.4161/auto.3632. Epub 2007 Mar 28.
The regulatory subunit 1-alpha (RIalpha) of protein kinase A (PKA) and the mTOR kinase are involved in a common pathway regulating mammalian autophagy. RIalpha was found to localize on Rab7-positive late endosomes and on LC3-positive autophagosomal membranes in cultured cells. RIalpha was also shown to physically interact with mTOR kinase and affect its phosphorylation and activity. In this addendum, we further explore the subcellular distribution of mTOR related to RIalpha and LC3. We present experiments showing that mTOR colocalizes with RIalpha-, Rab7- and LC3-positive membranes in cultured cells. Because RIalpha regulates the phosphorylation and activity of mTOR kinase, which we now show localizes on autophagosomal membranes, the possibility emerges that the RIalpha-mTOR complex acts at the level of autophagosome maturation.
蛋白激酶A(PKA)的调节亚基1-α(RIα)和mTOR激酶参与调控哺乳动物自噬的共同通路。研究发现,RIα定位于培养细胞中Rab7阳性的晚期内体和LC3阳性的自噬体膜上。RIα还被证明能与mTOR激酶发生物理相互作用,并影响其磷酸化和活性。在本附录中,我们进一步探究了与RIα和LC3相关的mTOR的亚细胞分布。我们展示的实验表明,mTOR在培养细胞中与RIα、Rab7和LC3阳性膜共定位。由于RIα调节mTOR激酶的磷酸化和活性,而我们现在表明mTOR定位于自噬体膜上,因此有可能RIα-mTOR复合物在自噬体成熟水平发挥作用。