Secreted midbody remnants are a class of extracellular vesicles molecularly distinct from exosomes and microparticles

During the final stages of cell division, newly-formed daughter cells remain connected by a thin intercellular bridge containing the midbody (MB), a microtubule-rich organelle responsible for cytokinetic abscission. Following cell division the MB is asymmetrically inherited by one daughter cell where it persists as a midbody remnant (MB-R). Accumulating evidence shows MB-Rs are secreted (sMB-Rs) into the extracellular medium and engulfed by neighbouring non-sister cells. While much is known about intracellular MB-Rs, sMB-Rs are poorly understood. Here, we report the large-scale purification and biochemical characterisation of sMB-Rs released from colon cancer cells, including profiling of their proteome using mass spectrometry. We show sMB-Rs are an abundant class of membrane-encapsulated extracellular vesicle (200-600nm) enriched in core cytokinetic proteins and molecularly distinct from exosomes and microparticles. Functional dissection of sMB-Rs demonstrated that they are engulfed by, and accumulate in, quiescent fibroblasts where they promote cellular transformation and an invasive phenotype. Rai et al. characterise the properties of secreted midbody remnants, showing they are distinct from exosomes and microvesicles. The authors also find that these vesicles are engulfed by cells and promote anchorage independent growth and invasive phenotypes in NIH3T3 fibroblasts.

Automated summary

The study characterized the properties of secreted midbody remnants from colon cancer cells, showing they are a distinct class of membrane-encapsulated extracellular vesicle enriched in core cytokinetic proteins. These sMB-Rs are engulfed by quiescent fibroblasts and promote cellular transformation and invasive phenotypes. The authors found that sMB-Rs are different from exosomes and microparticles, and play a role in promoting anchorage independent growth and invasive phenotypes in fibroblasts.