Evidence map›Paper›PMID 26293468›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2015

Monocyte-Derived Dendritic Cells Upregulate Extracellular Catabolism of Aggregated Low-Density Lipoprotein on Maturation, Leading to Foam Cell Formation.

Abigail S Haka, Rajesh K Singh, Inna Grosheva, Haley Hoffner, Estibaliz Capetillo-Zarate, Harvey F Chin, Niroshana Anandasabapathy, Frederick R Maxfield

Abstract readComparative Study
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Targeting Immune Senescence in Atherosclerosis.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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

8 authors at 1 institution in 1 country.

Abigail S HakaFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Rajesh K SinghFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Inna GroshevaFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Haley HoffnerFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Estibaliz Capetillo-ZarateFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Harvey F ChinFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Niroshana AnandasabapathyFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.).
Frederick R MaxfieldFrom the Department of Biochemistry, Weill Cornell Medical College, New York, NY (A.S.H., R.K.S., I.G., H.H., E.C.-Z., H.F.C., F.R.M.); and Department of Dermatology, Harvard Skin Disease Research Center, Bringham and Women's Hospital, Boston, MA (N.A.). frmaxfie@med.cornell.edu.
Hospital for Special Surgery · US

Funding

Macrophage-Lipoprotein InteractionsR01HL093324 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MAXFIELD, FREDERICK R. · 2009 to 2025
$6.7M
RECEPTOR-MEDIATED ENDOCYTOSIS: MECHANISM AND FUNCTIONR37DK027083 · NIDDK · WEILL MEDICAL COLL OF CORNELL UNIV · PI MAXFIELD, FREDERICK R. · 1993 to 2014
$6.5M
Isl1 and Wntbeta-catenin regulation of cardiac progenitor cellsR00HL092234 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KWON, CHULAN · 2011 to 2013
$730k
Isl1 and Wntbeta-catenin regulation of cardiac progenitor cellsK99HL092234 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI KWON, CHULAN · 2009 to 2010
$206k
NHLBI NIH HHS K99 HL092234NHLBI NIH HHS R00 HL092234NHLBI NIH HHS R01-HL092234NHLBI NIH HHS R01 HL093324NIDDK NIH HHS R37 DK027083NIDDK NIH HHS R37-DK27083
6 · The paper itself

Abstract

objectiveAlthough dendritic cells are known to play a role in atherosclerosis, few studies have examined the contribution of the wide variety of dendritic cell subsets. Accordingly, their roles in atherogenesis remain largely unknown. We investigated the ability of different dendritic cell subsets to become foam cells after contact with aggregated low-density lipoprotein (LDL; the predominant form of LDL found in atherosclerotic plaques). APPROACH AND

resultsWe demonstrate that both murine and human monocyte-derived dendritic cells use exophagy to degrade aggregated LDL, leading to foam cell formation, whereas monocyte-independent dendritic cells are unable to clear LDL aggregates by this mechanism. Exophagy is a catabolic process in which objects that cannot be internalized by phagocytosis (because of their size or association with extracellular structures) are initially digested in an extracellular acidic lytic compartment. Surprisingly, we found that monocyte-derived dendritic cells upregulate exophagy on maturation. This contrasts various forms of endocytic internalization in dendritic cells, which decrease on maturation. Finally, we show that our in vitro results are consistent with dendritic cell lipid accumulation in plaques of an ApoE(-/-) mouse model of atherosclerosis.

conclusionsOur results show that monocyte-derived dendritic cells use exophagy to degrade aggregated LDL and become foam cells, whereas monocyte-independent dendritic cells are unable to clear LDL deposits. Furthermore, we find that exophagy is upregulated on dendritic cell maturation. Thus, exophagy-mediated foam cell formation in monocyte-derived dendritic cells could play a significant role in atherogenesis.

Indexed as

AnimalsAtherosclerosisCells, CulturedDendritic CellsDisease Models, AnimalFoam CellsHumansLipoproteins, LDLMiceMice, KnockoutMonocytesPhagocytosisRandom AllocationTranscriptional ActivationUp-RegulationLipoproteins, LDLatherosclerosisdendritic cellsfoam cellsLDLlipoproteinsphagocytosis

Identifiers

PMID26293468
PMCPMC4583358
OpenAlexW2099097199

What OpenQuestion holds

Textmetadata
LicenceTDM
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.