Novel insights into mouse models of ectopic proplatelet release

Mature bone marrow (BM) megakaryocytes (MKs) produce platelets by extending proplatelets into sinusoidal blood vessels. Defects in this process can lead to thrombocytopenia and increased risk of bleeding. Mice lacking the actin-regulatory 2/3 complex (Arp2/3), or adhesion and degranulation-promoting adapter protein (ADAP) display thrombocytopenia and ectopic release of (pro)platelet-like particles into the BM compartment, pointing to an important axis of actin-mediated directional proplatelet formation. The mechanism underlying ectopic release in these mice is still not completely understood. However, we hypothesized that similar functional defects account for this observation. We analyzed WASp-, ADAP-, PFN1-, and ARPC2-knockout mice to determine the role of actin reorganization and integrin activation in directional proplatelet formation. ADAP-, ARPC2-, and PFN1-deficient MKs displayed reduced adhesion to collagen, defective F-actin organization, and diminished beta 1-integrin activation. WASp-deficient MKs showed the strongest reduction in the adhesion assay of collagen and altered F-actin organization with reduced podosome formation. Our results indicate that ADAP, PFN1, WASp, and ARP2/ 3 are part of the same pathway that regulates polarization processes in MKs and directional proplatelet formation into BM sinusoids.

Automated summary

Mature bone marrow megakaryocytes produce platelets through a mechanism involving actin regulation and integrin activation. Defects in this process can lead to thrombocytopenia and ectopic release of platelet-like particles. This study identifies several proteins that are part of the same pathway regulating directional proplatelet formation, providing insights into the underlying mechanisms and potential therapeutic targets.