Cell cycle-dependent centrosome clustering precedes proplatelet formation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 38896608.
- Also identified by DOI 10.1126/sciadv.adl6153 and PMC identifier 11186502.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Platelet-producing megakaryocytes (MKs) primarily reside in the bone marrow, where they duplicate their DNA content with each cell cycle resulting in polyploid cells with an intricate demarcation membrane system. While key elements of the cytoskeletal reorganizations during proplatelet formation have been identified, what initiates the release of platelets into vessel sinusoids remains largely elusive. Using a cell cycle indicator, we observed a unique phenomenon, during which amplified centrosomes in MKs underwent clustering following mitosis, closely followed by proplatelet formation, which exclusively occurred in G<sub>1</sub> of interphase. Forced cell cycle arrest in G<sub>1</sub> increased proplatelet formation not only in vitro but also in vivo following short-term starvation of mice. We identified that inhibition of the centrosomal protein kinesin family member C1 (KIFC1) impaired clustering and subsequent proplatelet formation, while KIFC1-deficient mice exhibited reduced platelet counts. In summary, we identified KIFC1- and cell cycle-mediated centrosome clustering as an important initiator of proplatelet formation from MKs.
Medical subject headings
- Centrosome
- Megakaryocytes
- Cell Cycle
- Blood Platelets
- Kinesins