Evidence map›Paper›PMID 42263231›Full record

ArticleJournal of the American Chemical Society2026

Tracking Gene Expression of Single Mitochondria in Live Neurons Using Nanotweezers.

Annie Sahota, Binoy Paulose Nadappuram, Siân C Allerton, Flavie Lesept, Jack H Howden, Suzanne Claxton, Yaxian Liu, Francesco A Aprile, Josef T Kittler, Michael J Devine and 2 more

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2026. 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.

No citing paper in PubMed yet.

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

12 authors.

Annie SahotaDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0003-2923-1550
Binoy Paulose NadappuramDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0002-1386-8357
Siân C AllertonDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.
Flavie LeseptDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, U.K.
Jack H HowdenDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, U.K.
Suzanne ClaxtonKinases and Brain Development Lab, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, U.K.
Yaxian LiuDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.
Francesco A AprileDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.
Josef T KittlerDepartment of Neuroscience, Physiology and Pharmacology, University College London, Gower Street, London WC1E 6BT, U.K.
Michael J DevineMitochondrial Neurobiology Lab, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, U.K.ORCID 0000-0001-6076-3382
Aleksandar P IvanovDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.
Joshua B EdelDepartment of Chemistry, Molecular Science Research Hub, Imperial College London, London W12 0BZ, U.K.ORCID 0000-0001-5870-8659

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurons are highly polarized cells that depend on mitochondria for energy and signaling homeostasis. Importantly, energy and signaling requirements vary considerably across individual neurons both spatially and temporally. Therefore, to fully understand neuronal mitochondria, methods are needed to analyze mitochondria in live cells over time. The nanotweezer, a minimally invasive single-cell sampling technique, enables precise extraction of individual mitochondria from defined subcellular locations. Here, we combine single-mitochondrial extraction from live neurons with targeted mitochondrial gene expression tracking and mtDNA profiling to develop a platform for live-cell single-mitochondrion tracking and analysis. By tracking the expression of specific mitochondrially encoded genes in the same neurons over time, we reveal preliminary data showing a downregulation of mitochondrial genes MT-ND1 and MT-ATP6 following exposure to α-synuclein aggregates, independent of the proximity of the aggregates to the sampled mitochondria. Our approach provides a proof-of-concept for precise, temporal measurements of mitochondrial composition and targeted gene expression

Indexed as

MitochondriaNanotechnologyNeuronsalpha-SynucleinAnimalsDNA, MitochondrialSingle-Cell Gene Expression Analysisalpha-SynucleinDNA, Mitochondrial

Identifiers

PMID42263231
PMCPMC13307273

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.