He Ruina, Peng Jingyu, Yuan Pengfei, Xu Fang, Wei Wensheng
a Biodynamic Optical Imaging Center (BIOPIC); Peking-Tsinghua Center for Life Sciences; State Key Laboratory of Protein and Plant Gene Research; School of Life Sciences; Peking University ; Beijing , China.
Autophagy. 2015;11(5):740-7. doi: 10.1080/15548627.2015.1034404.
BECN1/Beclin 1 is regarded as a critical component in the class III phosphatidylinositol 3-kinase (PtdIns3K) complex to trigger autophagy in mammalian cells. Despite its significant role in a number of cellular and physiological processes, the exact function of BECN1 in autophagy remains controversial. Here we created a BECN1 knockout human cell line using the TALEN technique. Surprisingly, the complete loss of BECN1 had little effect on LC3 (MAP1LC3B/LC3B) lipidation, and LC3B puncta resembling autophagosomes by fluorescence microscopy were still evident albeit significantly smaller than those in the wild-type cells. Electron microscopy (EM) analysis revealed that BECN1 deficiency led to malformed autophagosome-like structures containing multiple layers of membranes under amino acid starvation. We further confirmed that the PtdIns3K complex activity and autophagy flux were disrupted in BECN1(-/-) cells. Our results demonstrate the essential role of BECN1 in the functional formation of autophagosomes, but not in LC3B lipidation.
BECN1/Beclin 1被认为是III类磷脂酰肌醇3激酶(PtdIns3K)复合物中的关键成分,可在哺乳动物细胞中触发自噬。尽管它在许多细胞和生理过程中发挥着重要作用,但BECN1在自噬中的具体功能仍存在争议。在这里,我们使用TALEN技术创建了一个BECN1基因敲除的人类细胞系。令人惊讶的是,BECN1的完全缺失对LC3(MAP1LC3B/LC3B)脂化影响很小,通过荧光显微镜观察到的类似自噬体的LC3B斑点仍然明显,尽管比野生型细胞中的斑点小得多。电子显微镜(EM)分析显示,在氨基酸饥饿条件下,BECN1缺陷导致含有多层膜的畸形自噬体样结构。我们进一步证实,PtdIns3K复合物活性和自噬通量在BECN1(-/-)细胞中受到破坏。我们的结果表明,BECN1在自噬体的功能形成中起关键作用,但在LC3B脂化过程中并非如此。