Evidence map›Paper›PMID 31604801›Full record

ArticleThe Journal of cell biology2019

Insulin activates intracellular transport of lipid droplets to release triglycerides from the liver.

Mukesh Kumar, Srikant Ojha, Priyanka Rai, Alaumy Joshi, Siddhesh S Kamat, Roop Mallik

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Selective targeting of kinesin on lipid droplets in the liver reduces plasma lipids.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  11. Metabolic and immune-sensitive contacts between lipid droplets and endoplasmic reticulum reconstituted in vitro.Proceedings of the National Academy of Sciences of the United States of America · 2022
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  15. Oral Administration ofFrontiers in immunology · 2022
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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

6 authors at 2 institutions in 1 country.

Mukesh KumarDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Srikant OjhaDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Priyanka RaiDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India.
Alaumy JoshiDepartment of Biology, Indian Institute of Science Education and Research, Pune, India.
Siddhesh S KamatDepartment of Biology, Indian Institute of Science Education and Research, Pune, India.ORCID 0000-0001-6132-7574
Roop MallikDepartment of Biological Sciences, Tata Institute of Fundamental Research, Mumbai, India roop@tifr.res.in.ORCID 0000-0001-6820-6556
Tata Institute of Fundamental Research · INIndian Institute of Science Education and Research Pune · IN

Funding

DBT-Wellcome Trust India Alliance IA/S/19/2/504634Wellcome Trust
6 · The paper itself

Abstract

Triglyceride-rich lipid droplets (LDs) are catabolized with high efficiency in hepatocytes to supply fatty acids for producing lipoprotein particles. Fasting causes a massive influx of adipose-derived fatty acids into the liver. The liver in the fasted state is therefore bloated with LDs but, remarkably, still continues to secrete triglycerides at a constant rate. Here we show that insulin signaling elevates phosphatidic acid (PA) dramatically on LDs in the fed state. PA then signals to recruit kinesin-1 motors, which transport LDs to the peripherally located smooth ER inside hepatocytes, where LDs are catabolized to produce lipoproteins. This pathway is down-regulated homeostatically when fasting causes insulin levels to drop, thus preventing dangerous elevation of triglycerides in the blood. Further, we show that a specific peptide against kinesin-1 blocks triglyceride secretion without any apparent deleterious effects on cells. Our work therefore reveals fundamental mechanisms that maintain lipid homeostasis across metabolic states and leverages this knowledge to propose a molecular target against hyperlipidemia.

Indexed as

AnimalsBiological TransportCells, CulturedInsulinLipid DropletsLiverRatsRats, Sprague-DawleyTriglyceridesInsulinTriglycerides

Identifiers

PMID31604801
PMCPMC6829650
OpenAlexW2979855350

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.