Evidence map›Paper›PMID 38464175›Full record

ArticleResearch square2024

Subcellular functions of tau mediates repair response and synaptic homeostasis in injury.

David Grosshans, Riya Thomas, Die Zhang, Christopher Cronkite, Rintu Thomas, Sanjay Singh, Lawrence Bronk, Rodrigo Morales, Joseph Duman

Open access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

David GrosshansMD Anderson Cancer Center.
Riya Thomas
Die Zhang
Christopher Cronkite
Rintu Thomas
Sanjay Singh
Lawrence Bronk
Rodrigo MoralesThe University of Texas Health Science Center at Houston.ORCID 0000-0001-7766-5770
Joseph Duman
The University of Texas Health Science Center at Houston · USScripps MD Anderson Cancer Center · US

Funding

(PQ9) Directed and unbiased studies of synaptic injuries as sequelae of radiotherapy: mapping, sex-dependence, and reversalR01CA219667 · NCI · BAYLOR COLLEGE OF MEDICINE · PI DUMAN, JOSEPH G · 2017 to 2021
$2.6M
(PQ 9) Synaptic basis of deficits in attention and executive function following cranial radiationR01CA208535 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GROSSHANS, DAVID R · 2016 to 2020
$2.4M
Determining the optimal ion and fractionation scheme for the treatment of GBM in a comprehensive human organoid modelR01CA256848 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GROSSHANS, DAVID R · 2021 to 2025
$2.3M
Characterization of the cellular mechanisms of radiation induced brain necrosis for clinical interventionR01CA255596 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GROSSHANS, DAVID R · 2021 to 2025
$871k
NCI NIH HHS R01 CA208535NCI NIH HHS R01 CA219667NCI NIH HHS R01 CA255596NCI NIH HHS R01 CA256848
6 · The paper itself

Abstract

Injury responses in terminally differentiated cells such as neurons is tightly regulated by pathways aiding homeostatic maintenance. Cancer patients subjected to neuronal injury in brain radiation experience cognitive declines similar to those seen in primary neurodegenerative diseases. Numerous studies have investigated the effect of radiation in proliferating cells of the brain, yet the impact in differentiated, post-mitotic neurons, especially the structural and functional alterations remain largely elusive. We identified that microtubule-associated tau is a critical player in neuronal injury response via compartmentalized functions in both repair-centric and synaptic regulatory pathways. Ionizing radiation-induced injury acutely induces increase in phosphorylated tau in the nucleus and directly interacts with histone 2AX (H2AX), a DNA damage repair (DDR) marker. Loss of tau significantly reduced H2AX after irradiation, indicating that tau may play an important role in neuronal DDR response. We also observed that loss of tau increases eukaryotic elongation factor levels after irradiation, the latter being a positive regulator of protein translation. This cascades into a significant increase in synaptic proteins, resulting in disrupted homeostasis. Consequently, novel object recognition test showed decrease in learning and memory in tau-knockout mice after irradiation, and electroencephalographic activity showed increase in delta and theta band oscillations, often seen in dementia patients. Our findings demonstrate tau's previously undefined, multifunctional role in acute responses to injury, ranging from DDR response in the nucleus to synaptic function within a neuron. Such knowledge is vital to develop therapeutic strategies targeting neuronal injury in cognitive decline for at risk and vulnerable populations.

Identifiers

PMID38464175
PMCPMC10925419
OpenAlexW4392297386

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.