Evidence map›Paper›PMID 41803103›Full record

ArticleNature communications2026

Heterogeneity in lysosomal dynamics and metabolic functions along the kidney proximal tubule.

Monika Kaminska, Imene B Sakhi, Nevena Jankovic, Marcello Polesel, Andrew M Hall

Abstract read
In one paragraph

Article in Nature communications, 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

5 authors.

Monika Kaminska *Institute of Anatomy, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-6893-7815
Imene B Sakhi *Institute of Anatomy, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-8724-3459
Nevena JankovicInstitute of Anatomy, University of Zurich, Zurich, Switzerland.
Marcello PoleselInstitute of Anatomy, University of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-0668-8099
Andrew M HallInstitute of Anatomy, University of Zurich, Zurich, Switzerland. andrew.hall@uzh.ch.ORCID http://orcid.org/0000-0002-6328-7892

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The kidney proximal tubule is a highly specialized epithelium that transports metabolites and maintains body homeostasis. Cells lining this nephron segment are densely packed with lysosomes, but little is known about the dynamic activity of these organelles in situ. Here, using targeted sensors and live cell and intravital imaging we track acidified lysosomes along the mouse proximal tubule and uncover marked axial heterogeneity in their distribution, characteristics and organellar interactions. In the early part, cathepsin-rich lysosomes frequently contact with apical endosomes to receive and catabolize filtered plasma proteins. Conversely, in the later region, lipase-containing lysosomes traverse cells to mobilize and degrade mitochondria-associated lipid droplets and facilitate their extrusion into the tubular lumen. Acutely de-acidifying lysosomes dramatically alters their movement, causing major changes in tubular protein and lipid processing. Thus, lysosomes in proximal tubules are highly dynamic and adapted to perform distinct metabolic tasks within different specialized segments.

Indexed as

Kidney Tubules, ProximalLysosomesAnimalsCathepsinsEndosomesLipaseLipid MetabolismMaleMiceMitochondriaCathepsinsLipase

Identifiers

PMID41803103
PMCPMC13100021

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Registered trials

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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.