RAB-35 regulates distinct steps of trogocytosis in the biting and bitten cell

Trogocytosis is a form of cellular cannibalism in which a cell "bites" off pieces of another cell. Here, we investigate the molecular mechanisms of a developmentally programmed <i>C. elegans</i> trogocytic event that occurs when endodermal cells bite off and digest pieces of primordial germ cells (PGCs) called lobes. Through a genetic screen, we identify the Rab family small GTPase <i>rab-35</i> as a central regulator of trogocytosis and show that its function is required in both biting (endodermal) and bitten (PGC) cells. Within endodermal cells, RAB-35 enriches around trogocytosed PGC lobes, promotes the removal of phosphatidylinositol 4,5-bisphosphate (PIP <sub>2</sub> ), and is required for lobe digestion. By contrast, we show that RAB-35 within PGCs works with the ESCRT complex to promote scission of the PGC lobe from the cell body. Our findings identify a new regulator of trogocytosis that has distinct functions in the biting and bitten cells and provide evidence that the bitten cell contributes to the scission of its own membrane.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-02-22
DOI
https://doi.org/10.64898/2026.02.20.707090
Primary Topic
Genetics, Aging, and Longevity in Model Organisms
Type
article
Field-Weighted Citation Impact
0.00

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article

RAB-35 regulates distinct steps of trogocytosis in the biting and bitten cell

Yusuff Abdu, Jeremy Nance, Julie Manikas, Liam Popovsky
bioRxiv (Cold Spring Harbor Laboratory)
Genetics, Aging, and Longevity in Model Organisms
article

RAB-35 regulates distinct steps of trogocytosis in the biting and bitten cell

Yusuff Abdu, Jeremy Nance, Julie Manikas, Liam Popovsky
article en

Abstract

Trogocytosis is a form of cellular cannibalism in which a cell "bites" off pieces of another cell. Here, we investigate the molecular mechanisms of a developmentally programmed <i>C. elegans</i> trogocytic event that occurs when endodermal cells bite off and digest pieces of primordial germ cells (PGCs) called lobes. Through a genetic screen, we identify the Rab family small GTPase <i>rab-35</i> as a central regulator of trogocytosis and show that its function is required in both biting (endodermal) and bitten (PGC) cells. Within endodermal cells, RAB-35 enriches around trogocytosed PGC lobes, promotes the removal of phosphatidylinositol 4,5-bisphosphate (PIP <sub>2</sub> ), and is required for lobe digestion. By contrast, we show that RAB-35 within PGCs works with the ESCRT complex to promote scission of the PGC lobe from the cell body. Our findings identify a new regulator of trogocytosis that has distinct functions in the biting and bitten cells and provide evidence that the bitten cell contributes to the scission of its own membrane.

bioRxiv (Cold Spring Harbor Laboratory)
Quantitative BioSciences (US), Regenerative Medicine Institute (MX), New York University (US)
National Institutes of Health
Openalex Percentile: Top 46%
Genetics, Aging, and Longevity in Model Organisms
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