Evidence map›Paper›PMID 37872178›Full record

ArticleNature communications2023

Lipocalin 2 regulates mitochondrial phospholipidome remodeling, dynamics, and function in brown adipose tissue in male mice.

Hongming Su, Hong Guo, Xiaoxue Qiu, Te-Yueh Lin, Chao Qin, Gail Celio, Peter Yong, Mark Senders, Xianlin Han, David A Bernlohr and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.4field-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

20 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  7. Down-regulation of lipocalin-2 alleviates depressive-like behaviors in mice through modulation of microglial activation.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  8. Article
  9. Review
  10. Iron and the immune system.Nature reviews. Immunology · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Hongming SuDepartment of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, 55108, USA.ORCID http://orcid.org/0000-0002-9847-1825
Hong GuoDepartment of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, 55108, USA.ORCID http://orcid.org/0000-0001-8024-7086
Xiaoxue QiuDepartment of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, 55108, USA.ORCID http://orcid.org/0000-0002-1015-9993
Te-Yueh LinDepartment of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, 55108, USA.ORCID http://orcid.org/0000-0002-5541-445X
Chao QinBarshop Institute for Longevity and Aging Studies, Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229-3900, USA.
Gail CelioUniversity Imaging Centers, University of Minnesota-Twin Cities, Minneapolis, MN, 55455, USA.
Peter YongDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota-Twin Cities, Minneapolis, MN, 55455, USA.ORCID http://orcid.org/0000-0002-4899-3270
Mark SendersUniversity Imaging Centers, University of Minnesota-Twin Cities, Minneapolis, MN, 55455, USA.ORCID http://orcid.org/0000-0001-7550-5255
Xianlin HanBarshop Institute for Longevity and Aging Studies, Department of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX, 78229-3900, USA.ORCID http://orcid.org/0000-0002-8615-2413
David A BernlohrDepartment of Biochemistry, Molecular Biology and Biophysics, University of Minnesota-Twin Cities, Minneapolis, MN, 55455, USA.ORCID http://orcid.org/0000-0001-6969-9129
Xiaoli ChenDepartment of Food Science and Nutrition, University of Minnesota-Twin Cities, St. Paul, MN, 55108, USA. xlchen@umn.edu.ORCID http://orcid.org/0000-0003-3326-5390
University of Minnesota · USThe University of Texas Health Science Center at San Antonio · US

Funding

TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI JAMES FLOYD NELSON · 1995 to 2026
$30.6M
San Antonio OAIC - Research Education Component (REC)P30AG044271 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Adam Salmon, Elena Volpi · 2015 to 2026
$14.1M
Identification of a missing key element underlying apoE2 neuroprotection in Alzheimer's disease and the aging brainRF1AG061872 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HAN, XIANLIN, SESHADRI, SUDHA · 2018 to 2018
$3.4M
Lipocalin 2 as a regulator of phospholipid metabolism in adipose mitochondrial bioenergeticsR01DK123042 · NIDDK · UNIVERSITY OF MINNESOTA · PI CHEN, XIAOLI · 2020 to 2023
$1.9M
NIA NIH HHS P30 AG013319NIA NIH HHS P30 AG044271NIA NIH HHS RF1 AG061872NIDDK NIH HHS R01 DK123042
6 · The paper itself

Abstract

Mitochondrial function is vital for energy metabolism in thermogenic adipocytes. Impaired mitochondrial bioenergetics in brown adipocytes are linked to disrupted thermogenesis and energy balance in obesity and aging. Phospholipid cardiolipin (CL) and phosphatidic acid (PA) jointly regulate mitochondrial membrane architecture and dynamics, with mitochondria-associated endoplasmic reticulum membranes (MAMs) serving as the platform for phospholipid biosynthesis and metabolism. However, little is known about the regulators of MAM phospholipid metabolism and their connection to mitochondrial function. We discover that LCN2 is a PA binding protein recruited to the MAM during inflammation and metabolic stimulation. Lcn2 deficiency disrupts mitochondrial fusion-fission balance and alters the acyl-chain composition of mitochondrial phospholipids in brown adipose tissue (BAT) of male mice. Lcn2 KO male mice exhibit an increase in the levels of CLs containing long-chain polyunsaturated fatty acids (LC-PUFA), a decrease in CLs containing monounsaturated fatty acids, resulting in mitochondrial dysfunction. This dysfunction triggers compensatory activation of peroxisomal function and the biosynthesis of LC-PUFA-containing plasmalogens in BAT. Additionally, Lcn2 deficiency alters PA production, correlating with changes in PA-regulated phospholipid-metabolizing enzymes and the mTOR signaling pathway. In conclusion, LCN2 plays a critical role in the acyl-chain remodeling of phospholipids and mitochondrial bioenergetics by regulating PA production and its function in activating signaling pathways.

Indexed as

Adipose Tissue, BrownMitochondriaAdipocytes, BrownAnimalsLipocalin-2MaleMiceMice, Inbred C57BLMice, KnockoutPlasmalogensThermogenesisLcn2 protein, mouseLipocalin-2Plasmalogens

Identifiers

PMID37872178
PMCPMC10593768
OpenAlexW4387872532

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.