6 research outputs found
Platelet recovery and rebound thrombocytosis is enhanced in PKCĪµ<sup>-/-</sup> mice following immune-induced thrombocytopenia.
<p>A) PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> Mice were injected (I.P.) with 50 Ī¼g/kg anti-mouse CD41 antibody at day 0. Blood was collected daily via submandibular puncture for 5 days and again on day 7 and platelets were enumerated. * p < 0.05 compared to corresponding PKCĪµ<sup>+/+</sup> time point, n = 7. B) Representative images of proplatelet producing megakayrocytes. C) Quantitation of proplatelet production taken from several fields per experiment, expressed as a percentage of total megakaryocytes. *p < 0.05, n = 11.</p
Blood cell counts in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mice.
<p>Blood cell counts in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mice.</p
PKCĪµ<sup>-/-</sup> mice have a reduced LSK population, but a heightened megakaryocyte progenitor cell population.
<p>A) Schematic showing gates used to define each progenitor cell population. LK cells are defined as Lineage (Lin) negative cells that stain C-Kit+, Sca-1-. LSK cells stain Lin-, Sca-1+, C-Kit+. Megakaryocyte progenitors (MkP) are from the LK population and stain CD41+, CD150+. The LSK population is used to define multipotent progenitor cells (MPP), which stain CD105- and CD150-, as well as hematopoietic stem cells (HSC), which stain CD105+ and CD150+. B-F) Quantification of each progenitor cell population as defined in A in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mouse bone marrow expressed as a percentage of total bone marrow cells. * p < 0.05 compared to PKCĪµ<sup>+/+</sup>, n = 4.</p
PKC-epsilon deficiency alters progenitor cell populations in favor of megakaryopoiesis
<div><p>Background</p><p>It has long been postulated that Protein Kinase C (PKC) is an important regulator of megakaryopoiesis. Recent contributions to the literature have outlined the functions of several individual PKC isoforms with regard to megakaryocyte differentiation and platelet production. However, the exact role of PKCĪµ remains elusive.</p><p>Objective</p><p>To delineate the role of PKCĪµ in megakaryopoiesis.</p><p>Approach and results</p><p>We used a PKCĪµ knockout mouse model to examine the effect of PKCĪµ deficiency on platelet mass, megakaryocyte mass, and bone marrow progenitor cell distribution. We also investigated platelet recovery in PKCĪµ null mice and TPO-mediated signaling in PKCĪµ null megakaryocytes. PKCĪµ null mice have higher platelet counts due to increased platelet production compared to WT littermate controls (p<0.05, n = 8). Furthermore, PKCĪµ null mice have more bone marrow megakaryocyte progenitor cells than WT littermate control mice. Additionally, thrombopoietin-mediated signaling is perturbed in PKCĪµ null mice as Akt and ERK1/2 phosphorylation are enhanced in PKCĪµ null megakaryocytes stimulated with thrombopoietin. Finally, in response to immune-induced thrombocytopenia, PKCĪµ null mice recovered faster and had higher rebound thrombocytosis than WT littermate control mice.</p><p>Conclusions</p><p>Enhanced platelet recovery could be due to an increase in megakaryocyte progenitor cells found in PKCĪµ null mice as well as enhanced thrombopoietin-mediated signaling observed in PKCĪµ deficient megakaryocytes. These data suggest that PKCĪµ is a negative regulator of megakaryopoiesis.</p></div
Platelet mass is enhanced in PKCĪµ deficient mice.
<p>A) Western blot analysis of PKCĪµ, PKCĪ±, and PKCĪ“ in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mouse megakaryocytes (n = 3). Actin was used to assess loading. B) Platelet counts from PKCĪµ<sup>-/-</sup> and WT littermate control (PKCĪµ<sup>+/+</sup>) whole blood (n = 9). C) Reticulated ānewā platelets expressed as a percent of total blood cells in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mice (n = 6). D) Platelet clearance in PKCĪµ<sup>+/+</sup> and PKCĪµ<sup>-/-</sup> mice (n = 3). E) Representative images of femur sections stained with H&E. White arrows denote megakaryocytes. Images were captures used a Nikon E1000 microscope at 200X magnification. F) Quantitation of megakaryocytes per field of view (FOV). * p < 0.05, n = 11.</p
Megakaryocyte number is enhanced in PKCĪµ<sup>-/-</sup> bone marrow cultured with exogenous TPO.
<p>A) Megakaryocyte DNA content in PKCĪµ<sup>-/-</sup> and PKCĪµ<sup>+/+</sup> bone marrow cultured in the presence of 50 ng/mL TPO. B) Megakaryocyte number is cultured bone marrow from PKCĪµ<sup>-/-</sup> and PKCĪµ<sup>+/+</sup> mice supplemented with 50 ng/mL TPO. * p < 0.05 compared to PKCĪµ<sup>+/+</sup>, n = 7.</p