Effects of RNA interference of Atg4B on the limited proteolysis of LC3 in PC12 cells and expression of Atg4B in various rat tissues

被引:45
作者
Yoshimura, Kentaro
Shibata, Masahiro
Koike, Masato
Gotoh, Kunihito
Fukaya, Masahiro
Watanabe, Masahiko
Uchiyama, Yasuo
机构
[1] Osaka Univ, Grad Sch Med, Dept Cell Biol & Neurosci, Suita, Osaka 5650871, Japan
[2] Hokkaido Univ, Grad Sch Med, Dept Anat, Sapporo, Hokkaido, Japan
关键词
autophagy; Atg4; LC3; RNA interference; PC12; cells; rat tissues;
D O I
10.4161/auto.2744
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Atg4B, a mammalian homologue of yeast Atg4, has been shown to play an important role in the processing of LC3, a mammalian homologue of yeast Atg8, but the tissue distribution of Atg4B remains unknown. To better understand the role of Atg4B in rat tissue cells, we prepared antibodies against Atg4B, and PC 12 cells in which the expression of Atg4B was knocked down by RNA interference. In the RNA interference-treated PC 12 cells, for which the expression of Atg4B was 10% of wild-type PC 12 cells, the expression of cytosolic LC3-1 was similar to that in wild-type cells. Knockdown cell lysates, however, suppressed the cleavage of recombinant proLC3 to LC3-1. Moreover, the expression of Atg4B protein and mRNA was ubiquitous in rat tissues; however, the expression levels were not identical, but were dependent on the tissue, with the expression high in brain and testicular tissue, and low in muscular and heart tissue. In brain tissue, the expression of Atg4B protein and mRNA was higher in neurons, especially in the cerebellum and olfactory bulb, as evidenced by immunohistochemistry and in situ hybridization. These lines of evidence suggest that Atg4B plays a major role in the processing of LC3 and is widely distributed in rat tissues. In particular, in brain tissues, autophagy may be deeply associated with the metabolism of neurons, especially in the cerebellum.
引用
收藏
页码:200 / 208
页数:9
相关论文
共 42 条
  • [31] Coronavirus replication complex formation utilizes components of cellular autophagy
    Prentice, E
    Jerome, WG
    Yoshimori, T
    Mizushima, N
    Denison, MR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) : 10136 - 10141
  • [32] AUTOPHAGY AND OTHER VACUOLAR PROTEIN-DEGRADATION MECHANISMS
    SEGLEN, PO
    BOHLEY, P
    [J]. EXPERIENTIA, 1992, 48 (02): : 158 - 172
  • [33] Participation of cathepsins B and D in apoptosis of PC12 cells following serum deprivation
    Shibata, M
    Kanamori, S
    Isahara, K
    Ohsawa, Y
    Konishi, A
    Kametaka, S
    Watanabe, T
    Ebisu, S
    Ishido, K
    Kominami, E
    Uchiyama, Y
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 251 (01) : 199 - 203
  • [34] Structural basis for the specificity and catalysis of human Atg4B responsible for mammalian autophagy
    Sugawara, K
    Suzuki, NN
    Fujioka, Y
    Mizushima, N
    Ohsumi, Y
    Inagaki, F
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (48) : 40058 - 40065
  • [35] The crystal structure of microtubule-associated protein light chain 3, a mammalian homologue of Saccharomyces cerevisiae Atg8
    Sugawara, K
    Suzuki, NN
    Fujioka, Y
    Mizushima, N
    Ohsumi, Y
    Inagaki, F
    [J]. GENES TO CELLS, 2004, 9 (07) : 611 - 618
  • [36] HsAtg4B/HsApg4B/autophagin-1 cleaves the carboxyl termini of three human Atg8 homologues and delipidates microtubule-associated protein light chain 3-and GABAA receptor-associated protein-phospholipid conjugates
    Tanida, I
    Sou, YS
    Ezaki, J
    Minematsu-Ikeguchi, N
    Ueno, T
    Kominami, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (35) : 36268 - 36276
  • [37] Apg7p/Cvt2p: A novel protein-activating enzyme essential for autophagy
    Tanida, I
    Mizushima, N
    Kiyooka, M
    Ohsumi, M
    Ueno, T
    Ohsumi, Y
    Kominami, E
    [J]. MOLECULAR BIOLOGY OF THE CELL, 1999, 10 (05) : 1367 - 1379
  • [38] Human Apg3p/Aut1p homologue is an authentic E2 enzyme for multiple substrates, GATE-16, GABARAP, and MAP-LC3, and facilitates the conjugation of hApg12p to hApg5p
    Tanida, I
    Tanida-Miyake, E
    Komatsu, M
    Ueno, T
    Kominami, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (16) : 13739 - 13744
  • [39] The human homolog of Saccharomyces cerevisiae Apg7p is a protein-activating enzyme for multiple substrates including human Apg12p, GATE-16, GABARAP, and MAP-LC3
    Tanida, I
    Tanida-Miyake, E
    Ueno, T
    Kominami, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (03) : 1701 - 1706
  • [40] Human light chain 3/MAP1LC3B is cleaved at its carboxyl-terminal Met121 to expose Gly120 for lipidation and targeting to autophagosomal membranes
    Tanida, I
    Ueno, T
    Kominami, E
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (46) : 47704 - 47710