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Updated: Jul 16, 2026

In Situ Exploration of Murine Megakaryopoiesis using Transmission Electron Microscopy
Published on: September 8, 2021
Endomitotic megakaryocytes that form a bipolar spindle exhibit cleavage furrow ingression followed by furrow
Amy E Geddis1, Norma E Fox, Eugene Tkachenko
1Department of Pediatrics, Hematology-Oncology, University of California, San Diego, La Jolla, California 92093, USA. ageddis@ucsd.edu
Abstract:
Megakaryocyte (MK) differentiation is marked by the development of progressive polyploidy, due to repeated incomplete cell cycles in which mitosis is aborted during anaphase, a process termed endomitosis. We have postulated that anaphase in endomitotic MKs diverges from diploid mitosis at a point distal to the assembly of the midzone, possibly involving impaired cleavage furrow progression. To define the extent of furrow initiation and ingression in endomitosis, we performed time-lapse imaging of MKs expressing yellow fluorescent protein (YFP)-tubulin and monitored shape change as they progressed through anaphase. We found that in early endomitotic cells that have a bipolar spindle, cleavage furrows form that can undergo significant ingression, but furrows regress to produce polyploid cells. Compared to cells that divide, cells that exhibit furrow regression have a slower rate of furrow ingression and do not furrow as deeply. More highly polyploid MKs undergoing additional endomitotic cycles also show measurable furrowing that is followed by regression, but the magnitude of the shape change is less than seen in the early MKs. This suggests that in the earliest endomitotic cycles when there is formation of a bipolar spindle, the failure of cytokinesis occurs late, following assembly and initial constriction of the actin/myosin ring, whereas in endomitotic MKs that are already polyploid there is secondary inhibition of furrow progression. This behavior of furrow ingression followed by regression may explain why midbody remnants are occasionally observed in polyploid MKs. This finding has important implications for the potential mechanisms for cytokinesis failure in endomitosis.
Insights
Megakaryocyte (MK) polyploidy arises from endomitosis, where cell division fails. Studies show MKs initiate and ingress cleavage furrows, but these regress, leading to polyploidy and revealing mechanisms of cytokinesis failure.
Area of Science:
- Cell Biology
- Hematology
- Molecular Biology
Background:
- Megakaryocyte (MK) differentiation involves progressive polyploidy through endomitosis, a process of aborted mitosis.
- The precise point of failure in cytokinesis during endomitosis remains unclear, potentially involving impaired cleavage furrow progression.
Purpose of the Study:
- To define the extent of cleavage furrow initiation and ingression during endomitosis in MKs.
- To investigate the mechanisms underlying cytokinesis failure in developing polyploid MKs.
Main Methods:
- Time-lapse imaging of MKs expressing yellow fluorescent protein (YFP)-tubulin.
- Monitoring cellular shape changes during anaphase progression in endomitotic MKs.
Main Results:
- Early endomitotic MKs with bipolar spindles form and ingress cleavage furrows, but these furrows subsequently regress, resulting in polyploid cells.
- Furrow regression in MKs occurs at a slower rate and with less depth compared to cells that successfully divide.
- Highly polyploid MKs exhibit reduced furrow ingression and regression compared to earlier-stage MKs, suggesting secondary inhibition of furrow progression.
Conclusions:
- Cytokinesis failure in early endomitosis involves late failure after actin/myosin ring constriction, while in later stages, secondary inhibition of furrow progression occurs.
- Cleavage furrow ingression followed by regression in MK endomitosis may explain the occasional observation of midbody remnants.
- These findings provide insights into the mechanisms of cytokinesis failure during megakaryocyte polyploidization.
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