Evidence map›Paper›PMID 31577526›Full record

ArticleMolecular biology of the cell2019

Mitochondrial lipid droplet formation as a detoxification mechanism to sequester and degrade excessive urothelial membranes.

Yi Liao, Daniel K L Tham, Feng-Xia Liang, Jennifer Chang, Yuan Wei, Putty-Reddy Sudhir, Joseph Sall, Sarah J Ren, Javier U Chicote, Lora L Arnold and 10 more

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Oxidative Stress, Nutrition and Cancer: Friends or Foes?The world journal of men's health · 2021
    Review
  7. Review
  8. Review
  9. Short histological kaleidoscope - recent findings in histology. Part I.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

20 authors at 9 institutions in 4 countries.

Yi LiaoDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Daniel K L ThamDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Feng-Xia LiangDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Jennifer ChangDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Yuan WeiDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Putty-Reddy SudhirDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Joseph SallDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Sarah J RenDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Javier U ChicoteResearch Unit, Hospital Joan XXIII, Institut de Investigacio Sanitaria Pere Virgili (IISPV), Universitat Rovira i Virgili, Tarragona 43007, Spain.
Lora L ArnoldDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198.
Chih-Chi Andrew HuThe Wistar Institute, University of Pennsylvania, Philadelphia, PA 19104.
Rok RomihInstitute of Cell Biology, Faculty of Medicine, University of Ljubljana, SI-1000 Ljubljana, Slovenia.
Leonardo R AndradeSalk Institute, La Jolla, CA 92037.
Michael J RindlerDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
Samuel M CohenDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68198.
Rob DeSalleSackler Institute for Comparative Genomics, American Museum of Natural History, New York, NY 10024.
Antonio Garcia-EspañaResearch Unit, Hospital Joan XXIII, Institut de Investigacio Sanitaria Pere Virgili (IISPV), Universitat Rovira i Virgili, Tarragona 43007, Spain.
Mingxiao DingCollege of Life Sciences, Peking University, Dachengfang, Haidian, Beijing 100871, China.
Xue-Ru WuDepartment of Urology, New York University School of Medicine, New York, NY10016.
Tung-Tien SunDepartment of Cell Biology, New York University School of Medicine, New York, NY10016.
New York University · USInstitut de Recerca Biomèdica Catalunya Sud · ESUniversity of Nebraska Medical Center · USAmerican Museum of Natural History · USPeking University · CNSalk Institute for Biological Studies · USThe Wistar Institute · USUniversity of Ljubljana · SIVeterans Health Administration · US

Funding

Uroplakins and Baterial InfectionP01DK052206 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SUN, TUNG-TIEN · 1999 to 2015
$19.6M
Reagent/Service CoreP01CA165980 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WU, XUE-RU · 2013 to 2023
$13.5M
BIOCHEMISTRY OF UROTHELIAL DIFFERENTIATIONR01DK039753 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SUN, TUNG-TIEN · 1987 to 2012
$4.6M
Urothelial Stem CellsR01DK110466 · NIDDK · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WU, XUE-RU · 2017 to 2020
$2.6M
Scanning Electron Microscope with 3ViewS10OD019974 · OD · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI LIANG, FENGXIA · 2016 to 2016
$1.1M
Inverted two photon laser scanning microscope for host defenseS10RR023704 · NCRR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI DUSTIN, MICHAEL LORAN · 2008 to 2008
$500k
Zeiss LSM 710 confocal microscopeS10RR024708 · NCRR · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NANCE, JEREMY · 2009 to 2009
$438k
BLR&D Research Career Scientist Award ApplicationIK6BX004479 · VA · VA MEDICAL CENTER · PI WU, XUE-RU · 2019 to 2025
–
BLRD VA IK6 BX004479NCI NIH HHS P01 CA165980NCRR NIH HHS S10 RR023704NCRR NIH HHS S10 RR024708NIDDK NIH HHS P01 DK052206NIDDK NIH HHS R01 DK039753NIDDK NIH HHS R01 DK110466NIH HHS S10 OD019974
6 · The paper itself

Abstract

The apical surface of the terminally differentiated mammalian urothelial umbrella cell is mechanically stable and highly impermeable, in part due to its coverage by urothelial plaques consisting of 2D crystals of uroplakin particles. The mechanism for regulating the uroplakin/plaque level is unclear. We found that genetic ablation of the highly tissue-specific sorting nexin Snx31, which localizes to plaques lining the multivesicular bodies (MVBs) in urothelial umbrella cells, abolishes MVBs suggesting that Snx31 plays a role in stabilizing the MVB-associated plaques by allowing them to achieve a greater curvature. Strikingly, Snx31 ablation also induces a massive accumulation of uroplakin-containing mitochondria-derived lipid droplets (LDs), which mediate uroplakin degradation via autophagy/lipophagy, leading to the loss of apical and fusiform vesicle plaques. These results suggest that MVBs play an active role in suppressing the excessive/wasteful endocytic degradation of uroplakins. Failure of this suppression mechanism triggers the formation of mitochondrial LDs so that excessive uroplakin membranes can be sequestered and degraded. Because mitochondrial LD formation, which occurs at a low level in normal urothelium, can also be induced by disturbance in uroplakin polymerization due to individual uroplakin knockout and by arsenite, a bladder carcinogen, this pathway may represent an inducible, versatile urothelial detoxification mechanism.

Indexed as

AnimalsFemaleLipid DropletsMembrane GlycoproteinsMembranesMiceMice, Inbred C57BLMitochondriaMultivesicular BodiesSorting NexinsUrinary BladderUroplakinsUrotheliumMembrane GlycoproteinsSorting NexinsUroplakins

Identifiers

PMID31577526
PMCPMC6857570
OpenAlexW2977754800

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.