Evidence map›Paper›PMID 40579455›Full record

ArticleNature cell biology2025

The Vps13-like protein BLTP2 regulates phosphatidylethanolamine levels to maintain plasma membrane fluidity and breast cancer aggressiveness.

Subhrajit Banerjee, Stephan Daetwyler, Xiaofei Bai, Morgane Michaud, Juliette Jouhet, Derk Binns, Shruthi Madhugiri, Emma Johnson, Chao-Wen Wang, Reto Fiolka and 2 more

Abstract read
In one paragraph

Article in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Mechanistic dissection of BLTP2 targeting to ER-PM contact sites.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. ATG2 is a triglyceride transfer protein.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Subhrajit BanerjeeDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Stephan DaetwylerLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-7444-4734
Xiaofei BaiDepartment of Biology, University of Florida, Gainesville, FL, USA.
Morgane MichaudUniversité Grenoble Alpes, CNRS, CEA, INRAE, IRIG, LPCV, Grenoble, France.
Juliette JouhetUniversité Grenoble Alpes, CNRS, CEA, INRAE, IRIG, LPCV, Grenoble, France.
Derk BinnsDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Shruthi MadhugiriLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Emma JohnsonDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Chao-Wen WangDepartment of Life Sciences, National Cheng Kung University, Tainan, Taiwan.
Reto FiolkaLyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Alexandre ToulmayDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA. Alexandre.Toulmay@UTSouthwestern.edu.ORCID http://orcid.org/0009-0009-5383-3632
William A PrinzDepartment of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA. william.prinz@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-9053-2398

Funding

Technical Development Unit 2: Intelligent Hyperspectral Imaging of Subcellular Molecular States at the Whole Organ LevelU54CA268072 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI SEAN J MORRISON · 2021 to 2026
$9.1M
Biogenesis of the endoplasmic reticulumZIADK060105 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI PRINZ, WILLIAM · 2009 to 2022
$8.5M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
Transformative microscopes to image across spatiotemporal scalesR35GM133522 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI Reto Paul Fiolka · 2019 to 2026
$3.1M
Roles of endoplasmic reticulum subdomains in regulating intracellular lipid distribution and organelle biogenesisR35GM153315 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI William Prinz · 2024 to 2026
$1.2M
Modeling PIEZO associated diseases in Caenorhabditis elegans: from genetics to mechanismR00GM145224 · NIGMS · UNIVERSITY OF FLORIDA · PI BAI, XIAOFEI · 2023 to 2025
$727k
Agence Nationale de la Recherche (French National Research Agency) ANR-17-EURE-0003Center for Strategic Scientific Initiatives, National Cancer Institute (NCI Center for Strategic Scientific Initiatives) U54CA268072Intramural NIH HHS ZIA DK060105NCI NIH HHS U54 CA268072NIDDK NIH HHS P30 DK127984NIGMS NIH HHS R00 GM145224NIGMS NIH HHS R35 GM133522NIGMS NIH HHS R35 GM153315U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) U54CA268072U.S. Department of Health & Human Services | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (National Institute of Diabetes & Digestive & Kidney Diseases) ZIA DK060005U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM133522U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R35GM153315
6 · The paper itself

Abstract

Lipid transport proteins (LTPs) facilitate non-vesicular lipid exchange between cellular compartments and have critical roles in lipid homeostasis. A recently identified family of bridge-like LTPs (BLTPs) is thought to form lipid-transporting conduits between organelles. One of these, BLTP2, is conserved across species but its function is not known. Here we show that BLTP2 regulates plasma membrane (PM) fluidity by increasing phosphatidylethanolamine (PE) levels in the PM. BLTP2 localizes to endoplasmic reticulum (ER)-PM contact sites, and transports PE in vivo, suggesting it drives PE movement from ER to PM. We find that BLTP2 works in parallel with another pathway that regulates intracellular PE distribution and PM fluidity. BLTP2 expression correlates with breast cancer aggressiveness. We found that BLTP2 facilitates growth of a triple negative breast cancer cell line and sustains its aggressiveness in an in vivo model of metastasis, suggesting maintenance of PM fluidity by BLTP2 may be critical for tumorigenesis in humans.

Indexed as

Breast NeoplasmsCell MembraneMembrane FluidityPhosphatidylethanolaminesTriple Negative Breast NeoplasmsVesicular Transport ProteinsAnimalsCell Line, TumorCell ProliferationEndoplasmic ReticulumFemaleHumansMiceMice, NudeNeoplasm InvasivenessphosphatidylethanolaminePhosphatidylethanolaminesVesicular Transport Proteins

Identifiers

PMID40579455
PMCPMC12270902

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Registered trials

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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.