Evidence map›Paper›PMID 40742812›Full record

ArticleCell reports2025

Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells.

Jeffrey W Brown, Xiaobo Lin, Gabriel Anthony Nicolazzi, Xuemei Liu, Thanh Nguyen, Megan D Radyk, Joseph Burclaff, Jason C Mills

Abstract read
In one paragraph

Article in Cell reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Regulation of STK38 by autophagy governs YAP1 activity during paligenosis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Evidence that injury can causebioRxiv : the preprint server for biology · 2026
    Article
  6. Recent advances in spasmolytic polypeptide expressing metaplasia research.World journal of gastrointestinal oncology · 2026
    Review
  7. Article
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Jeffrey W BrownDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA. Electronic address: brownjw@wustl.edu.
Xiaobo LinDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA.
Gabriel Anthony NicolazziDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA.
Xuemei LiuDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA.
Thanh NguyenSection of Gastroenterology & Hepatology, Departments of Medicine, Pathology & Immunology, and Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Cancer and Cell Biology Graduate Program, Graduate School of Biomedical Sciences, Baylor College of Medicine, Houston, TX, USA.
Megan D RadykDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA.
Joseph BurclaffDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA.
Jason C MillsSection of Gastroenterology & Hepatology, Departments of Medicine, Pathology & Immunology, and Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA. Electronic address: jason.mills@bcm.edu.

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Wade Brown · 2000 to 2026
$30.8M
Tissue Analysis & Molecular Imaging CoreP30DK056338 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI Hashem B El-Serag · 2001 to 2026
$28.3M
REGULATION OF ATROPHY-INDUCED PROGENITOR CELLS IN THE GASTRIC CORPUSR01DK094989 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2012 to 2026
$6.1M
MECHANISMS OF CHIEF CELL DEDIFFERENTIATIONR01DK105129 · NIDDK · WASHINGTON UNIVERSITY · PI Jason C Mills · 2015 to 2026
$5.4M
Mechanisms Governing Expansion of Embryonic Progenitor Cells (EPCs) inMetaplasiaR01CA239645 · NCI · WASHINGTON UNIVERSITY · PI MILLS, JASON C · 2020 to 2024
$2.1M
Neoglycosylation Epitopes in Metaplasia and CancerK08DK132496 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Wade Brown · 2022 to 2026
$827k
Exploiting the Salivary Arsenal to Inhibit Diarrheal DiseaseR21AI156236 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BULLITT, ESTHER · 2021 to 2022
$466k
Transcriptional regulation of mitochondrial metabolism in human intestinal stem cellsK01DK140610 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Joseph R Burclaff · 2025 to 2026
$337k
Metabolic regulation of pancreatic metaplasia and neoplasiaK99GM159354 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI RADYK, MEGAN DEANNA · 2024 to 2025
$250k
Utility and feasibility of activity type to augment consumer wearable-based physical activity energy expenditure prediction equations using heartrate and movement in childrenF31DK136205 · NIDDK · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI WHITE III, JAMES W. · 2023 to 2024
$83k
Stress Pathways in the Induction of MetaplasiaF31CA236506 · NCI · WASHINGTON UNIVERSITY · PI RADYK, MEGAN DEANNA · 2019 to 2020
$58k
Investigating the roles and dynamics of the endoplasmic reticulum during paligenosis and metaplasia formationF31DK141249 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI NGUYEN, THANH · 2024 to 2024
$49k
NCI NIH HHS F31 CA236506NCI NIH HHS R01 CA239645NIAID NIH HHS R21 AI156236NIDDK NIH HHS F31 DK136205NIDDK NIH HHS F31 DK141249NIDDK NIH HHS K01 DK140610NIDDK NIH HHS K08 DK132496NIDDK NIH HHS P30 DK052574NIDDK NIH HHS P30 DK056338NIDDK NIH HHS R01 DK094989NIDDK NIH HHS R01 DK105129NIGMS NIH HHS K99 GM159354
6 · The paper itself

Abstract

Injury causes differentiated cells to undergo massive reprogramming to become proliferative and repair tissue via paligenosis. Gastric chief cells use paligenosis to reprogram into progenitor-like spasmolytic-polypeptide-expressing metaplasia (SPEM) cells. Stage 1 of paligenosis is the downscaling of mature cell architecture via a process involving lysosomes. Here, we notice that sulfated glycoproteins are not only digested during paligenosis but also excreted into the gland. Various genetic and pharmacological approaches show that endoplasmic reticulum membranes and secretory granule cargo are also excreted and that the process proceeds in parallel with but is mechanistically independent of autophagy. Three-dimensional light and electron microscopy demonstrated that excretion occurs via unique, complex, multi-chambered invaginations of the apical plasma membrane. As this lysosome-independent cell cleansing process does not seem to have been priorly described, we termed it "cathartocytosis." Cathartocytosis allows a cell to rapidly eject excess material without waiting for autophagic and lysosomal digestion, providing for efficient cellular downscaling.

Indexed as

Cell DifferentiationCellular ReprogrammingAnimalsAutophagyCell MembraneEndoplasmic ReticulumHumansLysosomesMiceCP: Cell biologyDas-1EPG5Rab7secretionsulfated mucins

Identifiers

PMID40742812
PMCPMC12478994

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.