Cell cycle–dependent centrosome clustering precedes proplatelet formation

Author:

Becker Isabelle C.12ORCID,Wilkie Adrian R.12,Nikols Emma1ORCID,Carminita Estelle12ORCID,Roweth Harvey G.23ORCID,Tilburg Julia12ORCID,Sciaudone Anthony R.3,Noetzli Leila J.23ORCID,Fatima Farheen1ORCID,Couldwell Genevieve3ORCID,Ray Anjana3,Mogilner Alex4ORCID,Machlus Kellie R.12ORCID,Italiano Joseph E.12ORCID

Affiliation:

1. Vascular Biology Program, Boston Children’s Hospital, 1 Blackfan Circle, Boston, MA 02115, USA.

2. Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.

3. Brigham and Women’s Hospital, 4 Blackfan Circle, Boston, MA 02115, USA.

4. Courant Institute of Mathematical Sciences, New York University, 251 Mercer Street, New York, NY 10012, USA.

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 1 of interphase. Forced cell cycle arrest in G 1 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.

Publisher

American Association for the Advancement of Science (AAAS)

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