Evidence map›Paper›PMID 40899996›Full record

ArticleThe Journal of cell biology2025

Multiple interactions recruit BLTP2 to ER-PM contacts to control plasma membrane dynamics.

Anbang Dai, Peng Xu, Chase Amos, Kenshiro Fujise, Yumei Wu, Han Yang, Julia N Eisen, Andrés Guillén-Samander, Pietro De Camilli

Abstract read
In one paragraph

Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Mechanistic dissection of BLTP2 targeting to ER-PM contact sites.bioRxiv : the preprint server for biology · 2026
    Article
  3. Subcellular Cartography of the Phosphoinositide Multiverse.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2026
    Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Anbang DaiDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-3434-0663
Peng XuDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-5197-9560
Chase AmosDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-3176-9387
Kenshiro FujiseDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-9018-6504
Yumei WuDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-0878-7605
Han YangDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-5431-5380
Julia N EisenDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-8152-2406
Andrés Guillén-SamanderDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-6882-3850
Pietro De CamilliDepartment of Neuroscience, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-9045-0723

Funding

Yale/NIDA Neuroproteomics Research CenterP30DA018343 · NIDA · YALE UNIVERSITY · PI Kenneth Robert WILLIAMS · 2004 to 2026
$37.1M
MOLECULAR MECHANISMS IN SYNAPTIC VESICLE RECYCLINGR01NS036251 · NINDS · YALE UNIVERSITY · PI DE CAMILLI, PIETRO · 1997 to 2021
$4.7M
Molecular Mechanisms in Synaptic Vesicle RecyclingR37NS036251 · NINDS · YALE UNIVERSITY · PI DE CAMILLI, PIETRO · 2010 to 2016
$2.7M
Short Term Research Training: Students in Health Professional SchoolsT35DK104689 · NIDDK · YALE UNIVERSITY · PI LLOYD G CANTLEY, Sarwat I Chaudhry · 2015 to 2026
$2.6M
Predoctoral Program in Cellular, Molecular and Quantitative Biology (CMQBTP)T32GM145469 · NIGMS · YALE UNIVERSITY · PI Susan J Baserga, Charles Patrick Lusk · 2023 to 2026
$2.2M
Investigation of the Lipid Transfer ProteinVPS13D at the Golgi ApparatusF31NS135930 · NINDS · YALE UNIVERSITY · PI Chase Allen Amos · 2025 to 2026
$100k
Gruber Science FellowshipNIDA NIH HHS P30 DA018343NIDDK NIH HHS T35 DK104689NIGMS NIH HHS T32 GM145469NIH HHS DA018343NIH HHS F31NS135930NIH HHS NS036251NIH HHS T32GM145469NIH HHS T35DK104689NINDS NIH HHS F31 NS135930NINDS NIH HHS R01 NS036251NINDS NIH HHS R37 NS036251
6 · The paper itself

Abstract

BLTP2/KIAA0100, a bridge-like lipid transfer protein, was reported to localize at contacts of the ER with either the plasma membrane (PM) or recycling tubular endosomes depending on the cell type. Our findings suggest that mediating bulk lipid transport between the ER and the PM is a key function of this protein, as BLTP2 tethers the ER to tubular endosomes only after they become continuous with the PM and that it also tethers the ER to macropinosomes in the process of fusing with the PM. We further identify interactions underlying binding of BLTP2 to the PM, including phosphoinositides, the adaptor proteins FAM102A/FAM102B, and N-BAR domain proteins at membrane-connected tubules. The absence of BLTP2 results in the accumulation of intracellular vacuoles, many of which are connected to the PM, pointing to a role of the lipid transport function of BLTP2 in the control of PM dynamics.

Indexed as

Carrier ProteinsCell MembraneEndoplasmic ReticulumAnimalsBiological TransportEndosomesHeLa CellsHumansPhosphatidylinositolsProtein BindingVacuolesCarrier ProteinsPhosphatidylinositols

Identifiers

PMID40899996
PMCPMC12406788

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.