Skip to Content
Merck
  • Microtubule sliding drives proplatelet elongation and is dependent on cytoplasmic dynein.

Microtubule sliding drives proplatelet elongation and is dependent on cytoplasmic dynein.

Blood (2014-11-21)
Markus Bender, Jonathan N Thon, Allen J Ehrlicher, Stephen Wu, Linas Mazutis, Emoke Deschmann, Martha Sola-Visner, Joseph E Italiano, John H Hartwig
ABSTRACT

Bone marrow megakaryocytes produce platelets by extending long cytoplasmic protrusions, designated proplatelets, into sinusoidal blood vessels. Although microtubules are known to regulate platelet production, the underlying mechanism of proplatelet elongation has yet to be resolved. Here we report that proplatelet formation is a process that can be divided into repetitive phases (extension, pause, and retraction), as revealed by differential interference contrast and fluorescence loss after photoconversion time-lapse microscopy. Furthermore, we show that microtubule sliding drives proplatelet elongation and is dependent on cytoplasmic dynein under static and physiological shear stress by using fluorescence recovery after photobleaching in proplatelets with fluorescence-tagged β1-tubulin. A refined understanding of the specific mechanisms regulating platelet production will yield strategies to treat patients with thrombocythemia or thrombocytopenia.

MATERIALS
Product Number
Brand
Product Description

Paclitaxel semi-synthetic for peak identification, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Nocodazole, ≥99% (TLC), powder
Paclitaxel semi-synthetic for system suitability, European Pharmacopoeia (EP) Reference Standard
Paclitaxel, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Paclitaxel, from semisynthetic, ≥98%
Sigma-Aldrich
Paclitaxel, from Taxus brevifolia, ≥95% (HPLC), powder
Sigma-Aldrich
Paclitaxel, from Taxus yannanensis, powder
Paclitaxel natural for peak identification, European Pharmacopoeia (EP) Reference Standard