Evidence map›Paper›PMID 41184966›Full record

ArticleCell communication and signaling : CCS2025

Cell-type-specific dysregulation of mitochondrial calcium signaling in Alzheimer's disease.

Shatakshi Shukla, Ashlesha A Kadam, Shanikumar Goyani, Natasha Jaiswal, Kunal Samantaray, Darpan Raghav, Shiridhar Kashyap, Dhanendra Tomar, Pooja Jadiya

Erratum issuedAbstract read
In one paragraph

Article in Cell communication and signaling : CCS, 2025. 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 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. Review
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Shatakshi ShuklaDepartment of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Ashlesha A KadamDepartment of Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Shanikumar GoyaniDepartment of Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Natasha JaiswalDepartment of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Kunal SamantarayDepartment of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Darpan RaghavDepartment of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Shiridhar KashyapDepartment of Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Dhanendra Tomar *Department of Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA. dhanendra.tomar@wfusm.edu.ORCID http://orcid.org/0000-0002-3144-7257
Pooja Jadiya *Department of Internal Medicine, Section of Gerontology and Geriatric Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA. pooja.jadiya@wfusm.edu.ORCID http://orcid.org/0000-0003-4807-9304

Funding

Wake Forest University School of Medicine Alzheimer's Disease Research CenterP30AG072947 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUZANNE CRAFT · 2021 to 2026
$24.3M
Impact of mitochondrial structure on cellular homeostasis and hepatic injuryR00DK120876 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI TOMAR, DHANENDRA · 2022 to 2024
$986k
Mitochondrial calcium uptake in Alzheimer's disease. Admin SupplementR00AG065445 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI JADIYA, POOJA · 2022 to 2024
$845k
American Heart Association 24IPA1273195American Heart Association 25CDA1454954American Heart Association 25POST1371847American Heart Association 25POST1378440NIA NIH HHS P30 AG072947NIA NIH HHS R00 AG065445NIDDK NIH HHS R00 DK120876NIH HHS R00AG065445NIH HHS R00DK120876
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by amyloid plaques, tau tangles, and synaptic dysfunction. Despite decades of research, effective disease-modifying therapies remain elusive, highlighting the need for alternative therapeutic targets. While neurons have traditionally been the focus of AD studies, increasing evidence underscores critical roles for glial cells particularly microglia and astrocytes in disease progression. Mitochondrial calcium (

methodsWe developed stable human SH-SY5Y (neuroblastoma-derived cells), HMC3 (microglial-like cells), and SVGp12 (astrocytic-like cells) immortalized cell lines expressing APP mutations (Swedish, Florida, and London; APPswe/F/L). We assessed mitochondrial calcium uniporter (mtCU) expression,

resultsAPPswe/F/L expression induced mitochondrial dysfunction across all brain immortalized cell types, with neuroblastoma-derived cells exhibiting the highest susceptibility to

conclusionsThis study reveals cell-type-specific differences in

Indexed as

Alzheimer DiseaseCalcium SignalingMitochondriaAstrocytesCalciumCalcium ChannelsCell LineCell Line, TumorHumansMicrogliaCalciumCalcium Channelsmitochondrial calcium uniporterAlzheimer’s diseaseCell deathCell-type specificityGlial-like cellsMitochondrial bioenergeticsMitochondrial calciumNeuroblastoma-derived cellsOxidative stress

Identifiers

PMID41184966
PMCPMC12581544

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.