Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells

Summary: 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 down...

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Main Authors: Jeffrey W. Brown, Xiaobo Lin, Gabriel Anthony Nicolazzi, Xuemei Liu, Thanh Nguyen, Megan D. Radyk, Joseph Burclaff, Jason C. Mills
Format: Article
Language:English
Published: Elsevier 2025-08-01
Series:Cell Reports
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Online Access:http://www.sciencedirect.com/science/article/pii/S2211124725008411
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author Jeffrey W. Brown
Xiaobo Lin
Gabriel Anthony Nicolazzi
Xuemei Liu
Thanh Nguyen
Megan D. Radyk
Joseph Burclaff
Jason C. Mills
author_facet Jeffrey W. Brown
Xiaobo Lin
Gabriel Anthony Nicolazzi
Xuemei Liu
Thanh Nguyen
Megan D. Radyk
Joseph Burclaff
Jason C. Mills
author_sort Jeffrey W. Brown
collection DOAJ
description Summary: 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.
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spelling doaj-art-5bc75d9afe5e46c1a4c0731944305dfc2025-08-20T03:09:34ZengElsevierCell Reports2211-12472025-08-0144811607010.1016/j.celrep.2025.116070Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cellsJeffrey W. Brown0Xiaobo Lin1Gabriel Anthony Nicolazzi2Xuemei Liu3Thanh Nguyen4Megan D. Radyk5Joseph Burclaff6Jason C. Mills7Division of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USA; Corresponding authorDivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USADivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USADivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USASection 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, USADivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USADivision of Gastroenterology, Department of Medicine, Washington University in St. Louis, School of Medicine, St. Louis, MO, USASection of Gastroenterology & Hepatology, Departments of Medicine, Pathology & Immunology, and Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Corresponding authorSummary: 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.http://www.sciencedirect.com/science/article/pii/S2211124725008411CP: Cell biology
spellingShingle Jeffrey W. Brown
Xiaobo Lin
Gabriel Anthony Nicolazzi
Xuemei Liu
Thanh Nguyen
Megan D. Radyk
Joseph Burclaff
Jason C. Mills
Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
Cell Reports
CP: Cell biology
title Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
title_full Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
title_fullStr Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
title_full_unstemmed Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
title_short Cathartocytosis: Jettisoning of cellular material during reprogramming of differentiated cells
title_sort cathartocytosis jettisoning of cellular material during reprogramming of differentiated cells
topic CP: Cell biology
url http://www.sciencedirect.com/science/article/pii/S2211124725008411
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