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Items: 1 to 20 of 88

1.
Tracking the transition from an ATG9A vesicle to an autophagosome
David Broadbent, Carlo Barnaba, Jens C. Schmidt
Autophagy. 2024; 20(4): 976–977. Published online 2023 Jul 26. doi: 10.1080/15548627.2023.2232641
PMCID:
PMC11062357
AbstractArticlePDF–231K
2.
The core autophagy protein ATG9A controls dynamics of cell protrusions and directed migration
Daniele Campisi, Laurence Desrues, Kléouforo-Paul Dembélé, Alexandre Mutel, Renaud Parment, Pierrick Gandolfo, Hélène Castel, Fabrice Morin
J Cell Biol. 2022 Mar 7; 221(3): e202106014. Published online 2022 Feb 18. doi: 10.1083/jcb.202106014
PMCID:
PMC8932524
AbstractArticlePDF–9.3M
3.
Structure, lipid scrambling activity and role in autophagosome formation of ATG9A
Shintaro Maeda, Hayashi Yamamoto, Lisa N. Kinch, Christina M. Garza, Satoru Takahashi, Chinatsu Otomo, Nick V. Grishin, Stefano Forli, Noboru Mizushima, Takanori Otomo
Nat Struct Mol Biol. Author manuscript; available in PMC 2021 Apr 26.
Published in final edited form as: Nat Struct Mol Biol. 2020 Dec; 27(12): 1194–1201. Published online 2020 Oct 26. doi: 10.1038/s41594-020-00520-2
PMCID:
PMC7718406
AbstractArticlePDF–2.4M
4.
The HIF target ATG9A is essential for epithelial barrier function and tight junction biogenesis
Alexander S. Dowdell, Ian M. Cartwright, Matthew S. Goldberg, Rachael Kostelecky, Tyler Ross, Nichole Welch, Louis E. Glover, Sean P. Colgan
Mol Biol Cell. 2020 Sep 15; 31(20): 2249–2258. doi: 10.1091/mbc.E20-05-0291
PMCID:
PMC7550696
AbstractArticlePDF–1.3M
5.
Structure of Human ATG9A, the Only Transmembrane Protein of the Core Autophagy Machinery
Carlos M. Guardia, Xiao-Feng Tan, Tengfei Lian, Mitra S. Rana, Wenchang Zhou, Eric T. Christenson, Augustus J. Lowry, José D. Faraldo-Gómez, Juan S. Bonifacino, Jiansen Jiang, Anirban Banerjee
Cell Rep. Author manuscript; available in PMC 2020 Jul 29.
Published in final edited form as: Cell Rep. 2020 Jun 30; 31(13): 107837. doi: 10.1016/j.celrep.2020.107837
PMCID:
PMC7388177
AbstractArticlePDF–3.6M
6.
The autophagy protein ATG9A promotes HIV-1 infectivity
Elodie Mailler, Abdul A. Waheed, Sang-Yoon Park, David C. Gershlick, Eric O. Freed, Juan S. Bonifacino
Retrovirology. 2019; 16: 18. Published online 2019 Jul 3. doi: 10.1186/s12977-019-0480-3
PMCID:
PMC6607583
AbstractArticlePDF–3.9M
7.
Deregulation of ATG9A by impaired AR signaling induces autophagy in prostate stromal fibroblasts and promotes BPH progression
Chen-Yi Jiang, Bo-Yu Yang, Sheng Zhao, Si-Hui Shao, Xiao-Yu Bei, Fei Shi, Qian Sun, Zheng Deng, Xiao-Hai Wang, Bang-Min Han, Fu-Jun Zhao, Shu-Jie Xia, Yuan Ruan
Cell Death Dis. 2018 Apr; 9(4): 431. Published online 2018 Mar 22. doi: 10.1038/s41419-018-0415-2
PMCID:
PMC5864884
AbstractArticlePDF–2.7M
8.
Excess sphingomyelin disturbs ATG9A trafficking and autophagosome closure
Elisabeth Corcelle-Termeau, Signe Diness Vindeløv, Saara Hämälistö, Baharia Mograbi, Anne Keldsbo, Jan Hinrich Bräsen, Elena Favaro, Dieter Adam, Piotr Szyniarowski, Paul Hofman, Stefan Krautwald, Thomas Farkas, Nikolaj H.T. Petersen, Mikkel Rohde, Andreas Linkermann, Marja Jäättelä
Autophagy. 2016 May; 12(5): 833–849. Published online 2016 Apr 12. doi: 10.1080/15548627.2016.1159378
PMCID:
PMC4854555
AbstractArticlePDF–2.5M
9.
ATG9B is a tissue-specific homotrimeric lipid scramblase that can compensate for ATG9A
George N. Chiduza, Acely Garza-Garcia, Eugenia Almacellas, Stefano De Tito, Valerie E Pye, Alexander R. van Vliet, Peter Cherepanov, Sharon A. Tooze
Autophagy. 2024; 20(3): 557–576. Published online 2023 Nov 8. doi: 10.1080/15548627.2023.2275905
PMCID:
PMC10936676
AbstractArticlePDF–6.1M
10.
ATG9A modulated by miR-195-5p can boost the malignant progression of cervical cancer cells
Xiaomin Liu, Zhen Liu, Yonggang Liu, Ning Wang
Epigenetics. 2023; 18(1): 2257538. Published online 2023 Oct 2. doi: 10.1080/15592294.2023.2257538
PMCID:
PMC10547073
AbstractArticlePDF–5.2M
11.
A novel role of ATG9A and RB1CC1/FIP200 in mediating cell-death checkpoints to repress TNF cytotoxicity
Ying Yang, Daniel J. Klionsky
Autophagy. 2023; 19(6): 1617–1618. Published online 2023 Mar 9. doi: 10.1080/15548627.2023.2187609
PMCID:
PMC10262787
AbstractArticlePDF–204K
12.
Quantitative analysis of autophagy reveals the role of ATG9 and ATG2 in autophagosome formation
David G. Broadbent, Carlo Barnaba, Gloria I. Perez, Jens C. Schmidt
J Cell Biol. 2023 Jul 3; 222(7): e202210078. Published online 2023 Apr 28. doi: 10.1083/jcb.202210078
PMCID:
PMC10148237
AbstractArticlePDF–9.0M
13.
The phosphatidylinositol 3-phosphate-binding protein SNX4 controls ATG9A recycling and autophagy
Anthony Ravussin, Andreas Brech, Sharon A. Tooze, Harald Stenmark
J Cell Sci. 2021 Feb 1; 134(3): jcs250670. Published online 2021 Feb 10. doi: 10.1242/jcs.250670
PMCID:
PMC7888711
AbstractArticle
14.
Activation of miR-34a impairs autophagic flux and promotes cochlear cell death via repressing ATG9A: implications for age-related hearing loss
Jiaqi Pang, Hao Xiong, Peiliang Lin, Lan Lai, Haidi Yang, Yimin Liu, Qiuhong Huang, Suijun Chen, Yongyi Ye, Yingfeng Sun, Yiqing Zheng
Cell Death Dis. 2017 Oct; 8(10): e3079. Published online 2017 Oct 5. doi: 10.1038/cddis.2017.462
PMCID:
PMC5680584
AbstractArticlePDF–1.7M
15.
Autophagy initiation by ULK complex assembly on ER tubulovesicular regions marked by ATG9 vesicles
Eleftherios Karanasios, Simon A. Walker, Hanneke Okkenhaug, Maria Manifava, Eric Hummel, Hans Zimmermann, Qashif Ahmed, Marie-Charlotte Domart, Lucy Collinson, Nicholas T. Ktistakis
Nat Commun. 2016; 7: 12420. Published online 2016 Aug 11. doi: 10.1038/ncomms12420
PMCID:
PMC4987534
AbstractArticlePDF–6.5M
16.
Methods to analyze SNARE-dependent vesicular fusion events that regulate autophagosome biogenesis
Kevin Moreau, Claudia Puri, David C Rubinsztein
Methods. 2015 Mar 15; 75: 19–24. doi: 10.1016/j.ymeth.2014.11.005
PMCID:
PMC4358838
AbstractArticlePDF–1.3M
17.
The autophagy protein ATG9A enables lipid mobilization from lipid droplets
Elodie Mailler, Carlos M. Guardia, Xiaofei Bai, Michal Jarnik, Chad D. Williamson, Yan Li, Nunziata Maio, Andy Golden, Juan S. Bonifacino
Nat Commun. 2021; 12: 6750. Published online 2021 Nov 19. doi: 10.1038/s41467-021-26999-x
PMCID:
PMC8605025
AbstractArticlePDF–16M
18.
AP-4 vesicles contribute to spatial control of autophagy via RUSC-dependent peripheral delivery of ATG9A
Alexandra K. Davies, Daniel N. Itzhak, James R. Edgar, Tara L. Archuleta, Jennifer Hirst, Lauren P. Jackson, Margaret S. Robinson, Georg H. H. Borner
Nat Commun. 2018; 9: 3958. Published online 2018 Sep 27. doi: 10.1038/s41467-018-06172-7
PMCID:
PMC6160451
AbstractArticlePDF–9.3M
19.
SNX18 regulates ATG9A trafficking from recycling endosomes by recruiting Dynamin‐2
Kristiane Søreng, Michael J Munson, Christopher A Lamb, Gunnveig T Bjørndal, Serhiy Pankiv, Sven R Carlsson, Sharon A Tooze, Anne Simonsen
EMBO Rep. 2018 Apr; 19(4): e44837. Published online 2018 Feb 7. doi: 10.15252/embr.201744837
PMCID:
PMC5891424
AbstractArticlePDF–1.6M
20.
AP-4 mediates export of ATG9A from the trans-Golgi network to promote autophagosome formation
Rafael Mattera, Sang Yoon Park, Raffaella De Pace, Carlos M. Guardia, Juan S. Bonifacino
Proc Natl Acad Sci U S A. 2017 Dec 12; 114(50): E10697–E10706. Published online 2017 Nov 27. doi: 10.1073/pnas.1717327114
PMCID:
PMC5740629
AbstractArticlePDF–3.3M

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