Evidence map›Paper›PMID 40204713›Full record

ArticleNature communications2025

GRAMD1B is a regulator of lipid homeostasis, autophagic flux and phosphorylated tau.

Diana Acosta Ingram, Emir Turkes, Tae Yeon Kim, Sheeny Vo, Nicholas Sweeney, Marie-Amandine Bonte, Ryan Rutherford, Dominic L Julian, Meixia Pan, Jacob Marsh and 13 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. The multimodal transcriptional response of denervated skeletal muscle involves regulation ofProceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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

23 authors.

Diana Acosta IngramDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Emir TurkesUK Dementia Research Institute, UCL Queen Square Institute of Neurology, London, UK.
Tae Yeon KimDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Sheeny VoDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Nicholas SweeneyDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Marie-Amandine BonteDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Ryan RutherfordThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Dominic L JulianThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.ORCID http://orcid.org/0000-0001-7352-4997
Meixia PanBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.
Jacob MarshDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.
Andrea R ArgouarchDepartment of Neurology, University of California, San Francisco, CA, USA.
Min WuDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA.
Douglas W ScharreDepartment of Neurology, College of Medicine, The Ohio State University, Columbus, OH, USA.
Erica H BellDepartment of Neurology, College of Medicine, The Ohio State University, Columbus, OH, USA.
Lawrence S HonigDepartment of Neurology, Columbia University Irving Medical Center, New York, NY, USA.ORCID http://orcid.org/0000-0002-9703-2265
Jean Paul VonsattelDepartment of Neurology, Columbia University Irving Medical Center, New York, NY, USA.
Geidy E SerranoBanner Sun Health Research Institute, Sun City, AZ, USA.
Thomas G BeachBanner Sun Health Research Institute, Sun City, AZ, USA.
Celeste M KarchDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0002-6854-5547
Aimee W KaoDepartment of Neurology, University of California, San Francisco, CA, USA.ORCID http://orcid.org/0000-0002-7686-7968
Mark E HesterThe Steve and Cindy Rasmussen Institute for Genomic Medicine, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.ORCID http://orcid.org/0000-0002-3726-4128
Xianlin HanBarshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA.ORCID http://orcid.org/0000-0002-8615-2413
Hongjun FuDepartment of Neuroscience, College of Medicine, The Ohio State University, Columbus, OH, USA. Hongjun.Fu@osumc.edu.ORCID http://orcid.org/0000-0001-5346-7075

Funding

Satellite Diagnostic and Treatment Clinic CoreP50AG008702 · NIA · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI SMALL, SCOTT A · 1989 to 2019
$46.3M
Research Education ComponentP30AG019610 · NIA · SUN HEALTH RESEARCH INSTITUTE · PI REIMAN, ERIC MICHAEL · 2001 to 2020
$32.5M
TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Xianlin Han · 1995 to 2026
$30.6M
Research Education CoreP30AG066462 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PHILIP L DE JAGER · 2020 to 2026
$30.1M
Research Education ComponentP30AG066444 · NIA · WASHINGTON UNIVERSITY · PI Susan Lynn Stark · 2020 to 2026
$28.7M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUANG, YADONG · 2004 to 2018
$27.1M
Research Education ComponentP30AG072980 · NIA · BANNER HEALTH · PI ALIREZA ATRI · 2021 to 2026
$24.9M
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
National Brain and Tissue Resource for Parkinson's Disease and Related DisordersU24NS072026 · NINDS · BANNER SUN HEALTH RESEARCH INSTITUTE · PI BEACH, THOMAS G · 2011 to 2015
$7.8M
Ectodermal-neural cortex 1 and neuronal vulnerability to tau pathology in Alzheimer's diseaseR01AG075092 · NIA · OHIO STATE UNIVERSITY · PI Hongjun Fu · 2022 to 2026
$2.4M
Targeting Tau Proteoforms in Frontotemporal DementiaRF1NS110890 · NINDS · WASHINGTON UNIVERSITY · PI KARCH, CELESTE MARIE · 2021 to 2021
$1.8M
Targeting Tau Proteoforms in Frontotemporal DementiaR01NS110890 · NINDS · WASHINGTON UNIVERSITY · PI KARCH, CELESTE MARIE · 2024 to 2024
$575k
BrightFocus Foundation (BrightFocus) A2021027SNIA NIH HHS P30 AG013319NIA NIH HHS P30 AG019610NIA NIH HHS P30 AG044271NIA NIH HHS P30 AG066444NIA NIH HHS P30 AG066462NIA NIH HHS P30 AG072980NIA NIH HHS P50 AG008702NIA NIH HHS P50 AG023501NIA NIH HHS R01 AG075092NINDS NIH HHS R01 NS110890NINDS NIH HHS R56 NS110890NINDS NIH HHS RF1 NS110890NINDS NIH HHS U24 NS072026U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) NS110890U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) AG066444U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) P30AG072980U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01-AG075092-01
6 · The paper itself

Abstract

Lipid dyshomeostasis and tau pathology are present in frontotemporal lobar degeneration (FTLD) and Alzheimer's disease (AD). However, the relationship between lipid dyshomeostasis and tau pathology remains unclear. We report that GRAM Domain Containing 1B (GRAMD1B), a nonvesicular cholesterol transporter, is increased in excitatory neurons of human neural organoids (HNOs) with the MAPT R406W mutation. Human FTLD, AD cases, and PS19 tau mice also have increased GRAMD1B expression. We show that overexpression of GRAMD1B increases levels of free cholesterol, lipid droplets, and impairs autophagy flux. Modulating GRAMD1B in iPSC-derived neurons also alters key autophagy-related components such as PI3K, phospho-AKT, and p62, as well as phosphorylated tau, and CDK5R1. Blocking GRAMD1B function decreases free cholesterol and lipid droplets. Knocking down GRAMD1B additionally reduces phosphorylated tau, and CDK5R1 expression. Our findings elucidate the role of GRAMD1B in the nervous system and highlight its relevance to FTLD and AD.

Indexed as

AutophagyLipid Metabolismtau ProteinsAlzheimer DiseaseAnimalsCholesterolFemaleFrontotemporal Lobar DegenerationHomeostasisHumansInduced Pluripotent Stem CellsLipid DropletsMaleMiceMice, TransgenicNeuronsCholesterolMAPT protein, humantau Proteins

Identifiers

PMID40204713
PMCPMC11982250

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.