Evidence map›Paper›PMID 35363568›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2022

Protective role of chaperone-mediated autophagy against atherosclerosis.

Julio Madrigal-Matute, Jenny de Bruijn, Kim van Kuijk, Dario F Riascos-Bernal, Antonio Diaz, Inmaculada Tasset, Adrián Martín-Segura, Marion J J Gijbels, Bianca Sander, Susmita Kaushik and 16 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
12.5field-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

70 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Review
  3. The Hallmarks of Aging: From Molecular Mechanisms to Clinical Translation.International journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Vascular Aging.Circulation · 2026
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Decoding Vascular Senescence: Cellular Insights and Therapeutic Strategies.International journal of biological sciences · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

10 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

26 authors at 7 institutions in 4 countries.

Julio Madrigal-MatuteDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Jenny de BruijnDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Kim van KuijkDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Dario F Riascos-BernalDepartment of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461.
Antonio DiazDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Inmaculada TassetDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Adrián Martín-SeguraDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Marion J J GijbelsDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Bianca SanderDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Susmita KaushikDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Erik A L BiessenDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Simoni TianoDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Mathieu BourdenxDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Gregory J KrauseDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Ian McCrackenCentre for Cardiovascular Science, University of Edinburgh, Edinburgh EH16 4TJ, United Kingdom.
Andrew H BakerDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.ORCID 0000-0003-1441-5576
Han JinDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.ORCID 0000-0002-0955-6289
Nicholas E S SibingaDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.
Jose Javier Bravo-CorderoDivision of Hematology and Medical Oncology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Fernando MacianInstitute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY 10461.
Rajat SinghDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.ORCID 0000-0001-9389-8574
Patrick C N RensenSection of Endocrinology, Department of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.ORCID 0000-0002-8455-4988
Jimmy F P BerbéeSection of Endocrinology, Department of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.
Gerard PasterkampExperimental Cardiology Laboratory, Department of Cardiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands.
Judith C SluimerDepartment of Pathology, Cardiovascular Research Institute Maastricht, Maastricht University Medical Center, 6229 HX Maastricht, The Netherlands.
Ana Maria CuervoDepartment of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461.ORCID 0000-0002-0771-700X
Albert Einstein College of Medicine · USMaastricht University · NLLeiden University Medical Center · NLMaastricht University Medical Centre · NLIcahn School of Medicine at Mount Sinai · USUniversity Medical Center Utrecht · NLUniversity of Edinburgh · GB

Funding

Role of Autophagy in T Cell Function and Immunosenescence (Project 3)P01AG031782 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2009 to 2024
$36.2M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007288 · NIGMS · YESHIVA UNIVERSITY · PI AKABAS, MYLES H. · 1985 to 2022
$35.6M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
Control of vesicular trafficking in the hepatocyte.R01DK098408 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA, WOLKOFF, ALLAN W · 2013 to 2022
$5.6M
Decreased Protein Degradation in AgingR37AG021904 · NIA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI CUERVO, ANA MARIA · 2013 to 2022
$4.4M
DECREASED PROTEIN DEGRADATION IN AGINGR01AG021904 · NIA · YESHIVA UNIVERSITY · PI CUERVO, ANA MARIA · 2003 to 2012
$3.7M
Metabolic control in vascular remodelingR01HL149921 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI SIBINGA, NICHOLAS E · 2020 to 2023
$2.4M
Regulation of T Cell Responses by Chaperone-Mediated AutophagyR01AI113919 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MACIAN, FERNANDO · 2016 to 2020
$2.1M
British Heart Foundation CH/11/2/28733British Heart Foundation RG/20/5/34796NHLBI NIH HHS R01 HL149921NIAID NIH HHS R01 AI113919NIA NIH HHS P01 AG031782NIA NIH HHS R01 AG021904NIA NIH HHS R37 AG021904NIDDK NIH HHS R01 DK098408NIGMS NIH HHS T32 GM007288NIGMS NIH HHS T32 GM007491
6 · The paper itself

Abstract

Chaperone-mediated autophagy (CMA) contributes to regulation of energy homeostasis by timely degradation of enzymes involved in glucose and lipid metabolism. Here, we report reduced CMA activity in vascular smooth muscle cells and macrophages in murine and human arteries in response to atherosclerotic challenges. We show that in vivo genetic blockage of CMA worsens atherosclerotic pathology through both systemic and cell-autonomous changes in vascular smooth muscle cells and macrophages, the two main cell types involved in atherogenesis. CMA deficiency promotes dedifferentiation of vascular smooth muscle cells and a proinflammatory state in macrophages. Conversely, a genetic mouse model with up-regulated CMA shows lower vulnerability to proatherosclerotic challenges. We propose that CMA could be an attractive therapeutic target against cardiovascular diseases.

Indexed as

AtherosclerosisChaperone-Mediated AutophagyAnimalsDisease Models, AnimalLysosomesMiceatherosclerotic plaqueslipid challengelysosomesproteolysisvascular disease

Identifiers

PMID35363568
PMCPMC9168839
OpenAlexW4221055778

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.