Evidence map›Paper›PMID 37014324›Full record

ArticleThe Journal of cell biology2023

ATG8-dependent LMX1B-autophagy crosstalk shapes human midbrain dopaminergic neuronal resilience.

Natalia Jiménez-Moreno, Madhu Kollareddy, Petros Stathakos, Joanna J Moss, Zuriñe Antón, Deborah K Shoemark, Richard B Sessions, Ralph Witzgall, Maeve Caldwell, Jon D Lane

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
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

16 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 3 countries.

Natalia Jiménez-MorenoCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0002-3934-7015
Madhu KollareddyCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0001-7412-096X
Petros StathakosCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0001-6661-9277
Joanna J MossCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0003-1690-6512
Zuriñe AntónCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0002-0175-8548
Deborah K ShoemarkSchool of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0002-1240-8463
Richard B SessionsSchool of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0003-0320-0895
Ralph WitzgallInstitute for Molecular and Cellular Anatomy, University of Regensburg , Regensburg, Germany.ORCID 0000-0002-5283-4846
Maeve CaldwellTrinity College Institute for Neuroscience, Trinity College Dublin , Dublin, Ireland.ORCID 0000-0001-7442-711X
Jon D LaneCell Biology Laboratories, School of Biochemistry, University of Bristol , Bristol, UK.ORCID 0000-0002-6828-5888
University of Bristol · GBTrinity College Dublin · IEUniversity of Regensburg · DE

Funding

Biotechnology and Biological Sciences Research Council BB/T016183/1Wellcome TrustWellcome Trust 083474
6 · The paper itself

Abstract

The LIM homeodomain transcription factors LMX1A and LMX1B are essential mediators of midbrain dopaminergic neuronal (mDAN) differentiation and survival. Here we show that LMX1A and LMX1B are autophagy transcription factors that provide cellular stress protection. Their suppression dampens the autophagy response, lowers mitochondrial respiration, and elevates mitochondrial ROS, and their inducible overexpression protects against rotenone toxicity in human iPSC-derived mDANs in vitro. Significantly, we show that LMX1A and LMX1B stability is in part regulated by autophagy, and that these transcription factors bind to multiple ATG8 proteins. Binding is dependent on subcellular localization and nutrient status, with LMX1B interacting with LC3B in the nucleus under basal conditions and associating with both cytosolic and nuclear LC3B during nutrient starvation. Crucially, ATG8 binding stimulates LMX1B-mediated transcription for efficient autophagy and cell stress protection, thereby establishing a novel LMX1B-autophagy regulatory axis that contributes to mDAN maintenance and survival in the adult brain.

Indexed as

Autophagy-Related Protein 8 FamilyLIM-Homeodomain ProteinsMesencephalonNeuronsTranscription FactorsAutophagyBrainHumansAutophagy-Related Protein 8 FamilyGABARAPL2 protein, humanLIM homeobox transcription factor 1 betaLIM-Homeodomain ProteinsTranscription Factors

Identifiers

PMID37014324
PMCPMC10075225
OpenAlexW4362522051

What OpenQuestion 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 OpenQuestion graph.