Evidence map›Paper›PMID 35982578›Full record

ArticleAutophagy2023

Use of acidic nanoparticles to rescue macrophage lysosomal dysfunction in atherosclerosis.

Xiangyu Zhang, Santosh Kumar Misra, Parikshit Moitra, Xiuli Zhang, Se-Jin Jeong, Jeremiah Stitham, Astrid Rodriguez-Velez, Arick Park, Yu-Sheng Yeh, William E Gillanders and 7 more

Open access · greenAbstract read
In one paragraph

Article in Autophagy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

35 citing papers in PubMed, 43 citations in OpenAlex.

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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

17 authors at 5 institutions in 2 countries.

Xiangyu ZhangCardiovascular Division, Washington University, St. Louis, MO, USA.
Santosh Kumar MisraDepartment of Bioengineering, University of Illinois at Urbana Champaign, IL, USA.
Parikshit MoitraDepartments of Diagnostic Radiology and Nuclear Medicine and Pediatrics, Baltimore, Maryland, USA.
Xiuli ZhangDepartment of Surgery, Washington University, St. Louis, MO, USA.
Se-Jin JeongCardiovascular Division, Washington University, St. Louis, MO, USA.
Jeremiah StithamCardiovascular Division, Washington University, St. Louis, MO, USA.
Astrid Rodriguez-VelezCardiovascular Division, Washington University, St. Louis, MO, USA.
Arick ParkCardiovascular Division, Washington University, St. Louis, MO, USA.
Yu-Sheng YehCardiovascular Division, Washington University, St. Louis, MO, USA.
William E GillandersDepartment of Surgery, Washington University, St. Louis, MO, USA.
Daping FanDepartment of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, SC, USA.
Abhinav DiwanCardiovascular Division, Washington University, St. Louis, MO, USA.
Jaehyung ChoDivision of Hematology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA.
Slava EpelmanPeter Munk Cardiac Center, Toronto General Hospital Research Institute, University Health Network, Ted Rogers Centre for Heart Research, University of Toronto, Toronto, Ontario, Canada.
Irfan J LodhiDivision of Endocrinology, Metabolism, and Lipid Research, St. Louis, MO, USA.
Dipanjan PanDepartment of Bioengineering, University of Illinois at Urbana Champaign, IL, USA.
Babak RazaniCardiovascular Division, Washington University, St. Louis, MO, USA.ORCID 0000-0002-7172-9240
Washington University in St. Louis · USPennsylvania State University · USUniversity Health Network · CAUniversity of Illinois Urbana-Champaign · USUniversity of South Carolina · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Brian N Finck · 1999 to 2026
$30.2M
PRINCIPLES IN CARDIVASCULAR RESEARCH TRAINING PROGRAMT32HL007081 · NHLBI · WASHINGTON UNIVERSITY · PI Abhinav Diwan, Karen Ellen Joynt Maddox · 1985 to 2026
$10.6M
ROLE OF AUTOPHAGIC FLUX IN CARDIAC MYOCYTE VIABILITYR01HL107594 · NHLBI · WASHINGTON UNIVERSITY · PI Abhinav Diwan · 2011 to 2026
$5.9M
THE ROLE OF MACROPHAGE LYSOSOMAL BIOGENESIS IN ATHEROSCLEROSISR01HL125838 · NHLBI · WASHINGTON UNIVERSITY · PI RAZANI, BABAK · 2015 to 2025
$4.6M
Thiol isomerases in neutrophil recruitment and thromboinflammatory diseaseR01HL130028 · NHLBI · WASHINGTON UNIVERSITY · PI CHO, JAEHYUNG · 2016 to 2024
$3.6M
Dissecting the Impact of Dietary Protein on Macrophage mTOR Signaling and AtherosclerosisR01HL159461 · NHLBI · WASHINGTON UNIVERSITY · PI Bettina Mittendorfer, Babak Razani · 2022 to 2026
$3.3M
Animal and plant proteins and glucose metabolismR01DK121560 · NIDDK · WASHINGTON UNIVERSITY · PI KLEIN, SAMUEL, MITTENDORFER, BETTINA · 2019 to 2023
$2.8M
Harnessing macrophage lysosomal lipid metabolism in obesity-associated diseasesR01DK131188 · NIDDK · WASHINGTON UNIVERSITY · PI MITTENDORFER, BETTINA, RAZANI, BABAK · 2022 to 2025
$2.6M
Protein disulfide isomerase in neutrophil recruitment and vascular inflammationR01HL109439 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI CHO, JAEHYUNG · 2011 to 2015
$2.0M
Mitochondrial dynamics and the control of adipose tissue thermogenesisR01DK132239 · NIDDK · WASHINGTON UNIVERSITY · PI Irfan J Lodhi · 2022 to 2026
$1.9M
REGULATION OF ADIPOSE TISSUE REMODELING AND ENERGY HOMEOSTASISR01DK115867 · NIDDK · WASHINGTON UNIVERSITY · PI LODHI, IRFAN J · 2018 to 2022
$1.9M
Thiol isomerases and ERO1α in sickle cell vaso-occlusionR01HL148280 · NHLBI · WASHINGTON UNIVERSITY · PI CHO, JAEHYUNG · 2019 to 2022
$1.9M
BLRD VA I01 BX003415BLRD VA I01 BX004235BLRD VA I01 BX005981NHLBI NIH HHS R01 HL107594NHLBI NIH HHS R01 HL109439NHLBI NIH HHS R01 HL125838NHLBI NIH HHS R01 HL130028NHLBI NIH HHS R01 HL146559NHLBI NIH HHS R01 HL148280NHLBI NIH HHS R01 HL153047NHLBI NIH HHS R01 HL159461NHLBI NIH HHS R43 HL151073NHLBI NIH HHS T32 HL007081NHLBI NIH HHS T32 HL134635NIBIB NIH HHS R03 EB028026NIDCR NIH HHS R03 DE028026NIDDK NIH HHS P30 DK056341NIDDK NIH HHS R01 DK115867NIDDK NIH HHS R01 DK118333NIDDK NIH HHS R01 DK121560NIDDK NIH HHS R01 DK131188NIDDK NIH HHS R01 DK132239
6 · The paper itself

Abstract

Dysfunction in the macrophage lysosomal system including reduced acidity and diminished degradative capacity is a hallmark of atherosclerosis, leading to blunted clearance of excess cellular debris and lipids in plaques and contributing to lesion progression. Devising strategies to rescue this macrophage lysosomal dysfunction is a novel therapeutic measure. Nanoparticles have emerged as an effective platform to both target specific tissues and serve as drug delivery vehicles. In most cases, administered nanoparticles are taken up non-selectively by the mononuclear phagocyte system including monocytes/macrophages leading to the undesirable degradation of cargo in lysosomes. We took advantage of this default route to target macrophage lysosomes to rectify their acidity in disease states such as atherosclerosis. Herein, we develop and test two commonly used acidic nanoparticles, poly-lactide-co-glycolic acid (PLGA) and polylactic acid (PLA), both

Indexed as

AtherosclerosisNanoparticlesPlaque, AtheroscleroticAcidsAutophagyGlycolatesHumansLysosomesMacrophagesPolyestersAcidsGlycolatesglycolic acidPolyestersAcidic nanoparticlesatherosclerosislysosomal dysfunctionmacrophagePLGA

Identifiers

PMID35982578
PMCPMC9980706
OpenAlexW4292680234

What OpenQuestion holds

Textmetadata
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.