Evidence map›Paper›PMID 38600097›Full record

ArticleNature communications2024

Integrated proteomics reveals autophagy landscape and an autophagy receptor controlling PKA-RI complex homeostasis in neurons.

Xiaoting Zhou, You-Kyung Lee, Xianting Li, Henry Kim, Carlos Sanchez-Priego, Xian Han, Haiyan Tan, Suiping Zhou, Yingxue Fu, Kerry Purtell and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
12.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 31 citations in OpenAlex.

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  14. Biogenesis and reformation of synaptic vesicles.The Journal of physiology · 2025
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Turning garbage into gold: Autophagy in synaptic function.Current opinion in neurobiology · 2025
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 3 countries.

Xiaoting ZhouDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
You-Kyung LeeDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0002-0818-0080
Xianting LiDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0002-3153-0931
Henry KimDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Carlos Sanchez-PriegoNash Family Department of Neuroscience, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0009-0008-3151-086X
Xian HanDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Haiyan TanDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID http://orcid.org/0000-0001-6687-2563
Suiping ZhouCenter for Proteomics and Metabolomics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Yingxue FuDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID http://orcid.org/0000-0003-3052-4131
Kerry PurtellDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Qian WangDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.
Gay R HolsteinDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA.ORCID http://orcid.org/0000-0002-9463-8245
Beisha TangDepartment of Neurology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China.ORCID http://orcid.org/0000-0003-2120-1576
Junmin PengDepartment of Structural Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. junmin.peng@stjude.org.ORCID http://orcid.org/0000-0003-0472-7648
Nan YangNash Family Department of Neuroscience, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. nan.yang1@mssm.edu.ORCID http://orcid.org/0000-0003-3663-1288
Zhenyu YueDepartment of Neurology, The Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY, 10029, USA. zhenyu.yue@mssm.edu.ORCID http://orcid.org/0000-0001-8730-8515
Allen Institute for Brain Science · USSt. Jude Children's Research Hospital · USCentral South University · CN

Funding

Neuronal Autophagy: a Cell-Autonomous Protection MechanismR01NS060123 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Zhenyu Yue · 2008 to 2026
$9.2M
Determining the neuroprotective mechanism for microglial autophagy in Alzheimer's diseaseR01AG072520 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI YUE, ZHENYU · 2021 to 2025
$4.2M
Determining Selective Autophagy Kinase in Modulating Neurotoxicity in Huntington's Disease ModelR01NS117590 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI YUE, ZHENYU · 2020 to 2024
$2.3M
Determining neuroprotective autophagy functions using different types of human neuronsR21AG067570 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI YANG, NAN, YUE, ZHENYU · 2020 to 2020
$466k
NIA NIH HHS R01 AG072520NIA NIH HHS R21 AG067570NINDS NIH HHS R01 NS060123NINDS NIH HHS R01 NS117590
6 · The paper itself

Abstract

Autophagy is a conserved, catabolic process essential for maintaining cellular homeostasis. Malfunctional autophagy contributes to neurodevelopmental and neurodegenerative diseases. However, the exact role and targets of autophagy in human neurons remain elusive. Here we report a systematic investigation of neuronal autophagy targets through integrated proteomics. Deep proteomic profiling of multiple autophagy-deficient lines of human induced neurons, mouse brains, and brain LC3-interactome reveals roles of neuronal autophagy in targeting proteins of multiple cellular organelles/pathways, including endoplasmic reticulum (ER), mitochondria, endosome, Golgi apparatus, synaptic vesicle (SV) for degradation. By combining phosphoproteomics and functional analysis in human and mouse neurons, we uncovered a function of neuronal autophagy in controlling cAMP-PKA and c-FOS-mediated neuronal activity through selective degradation of the protein kinase A - cAMP-binding regulatory (R)-subunit I (PKA-RI) complex. Lack of AKAP11 causes accumulation of the PKA-RI complex in the soma and neurites, demonstrating a constant clearance of PKA-RI complex through AKAP11-mediated degradation in neurons. Our study thus reveals the landscape of autophagy degradation in human neurons and identifies a physiological function of autophagy in controlling homeostasis of PKA-RI complex and specific PKA activity in neurons.

Indexed as

NeuronsProteomicsAnimalsAutophagyCyclic AMP-Dependent Protein KinasesHomeostasisHumansMiceCyclic AMP-Dependent Protein Kinases

Identifiers

PMID38600097
PMCPMC11006854
OpenAlexW4394689401

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.