Mnk1 regulates megakaryocyte endomitosis and platelet production. (A) Pearson correlation analyses of the association between platelet counts (left) and MPV (right) with platelet MKNK1 mRNA expression (n = 154 healthy human donors). Light gray lines represent 95% confidence intervals. (B) Platelet counts (left) and mean platelet volume (right) in WT or Mnk1 KO mice (n > 10 mice per group, ∗P < .05). (C) Bone marrow–derived megakaryocytes from WT or Mnk1 KO mice were collected at culture day 5, and ploidy distribution of megakaryocytes was quantified (n = 3 independent experiments), ∗PANOVA < .05). (D) Bone marrow–derived megakaryocytes from WT or Mnk1 KO mice were collected at culture day 5. Megakaryocytes were then allowed to adhere to fibrinogen-coated plates and incubated overnight at 37°C. Megakaryocytes were then stained with phalloidin, and proplatelet formation was assessed by confocal microscopy. The right bar graph shows the number of proplatelet forming megakaryocytes (∗P < .05, n = 3 independent experiments). (E-F) Platelets were depleted from WT or Mnk1 KO mice by a single IV injection of an anti-GPIbα antibody (Emfret Analytics), leading to near-complete platelet clearance by 48 hours. Platelet counts were measured over 120 hours (eg, 5 days) by Hemavet. The (E) percentage of platelet count recovery was calculated from the platelet nadir at 48 hours, and (F) platelet clearance was calculated from the time of injection of the anti-GPIbα antibody (n = 5 mice per group, ∗P < .05; ∗∗P < .01). ANOVA, analysis of variance; NS, not significant.
Figure 3.

Mnk1 regulates megakaryocyte endomitosis and platelet production. (A) Pearson correlation analyses of the association between platelet counts (left) and MPV (right) with platelet MKNK1 mRNA expression (n = 154 healthy human donors). Light gray lines represent 95% confidence intervals. (B) Platelet counts (left) and mean platelet volume (right) in WT or Mnk1 KO mice (n > 10 mice per group, ∗P < .05). (C) Bone marrow–derived megakaryocytes from WT or Mnk1 KO mice were collected at culture day 5, and ploidy distribution of megakaryocytes was quantified (n = 3 independent experiments), ∗PANOVA < .05). (D) Bone marrow–derived megakaryocytes from WT or Mnk1 KO mice were collected at culture day 5. Megakaryocytes were then allowed to adhere to fibrinogen-coated plates and incubated overnight at 37°C. Megakaryocytes were then stained with phalloidin, and proplatelet formation was assessed by confocal microscopy. The right bar graph shows the number of proplatelet forming megakaryocytes (∗P < .05, n = 3 independent experiments). (E-F) Platelets were depleted from WT or Mnk1 KO mice by a single IV injection of an anti-GPIbα antibody (Emfret Analytics), leading to near-complete platelet clearance by 48 hours. Platelet counts were measured over 120 hours (eg, 5 days) by Hemavet. The (E) percentage of platelet count recovery was calculated from the platelet nadir at 48 hours, and (F) platelet clearance was calculated from the time of injection of the anti-GPIbα antibody (n = 5 mice per group, ∗P < .05; ∗∗P < .01). ANOVA, analysis of variance; NS, not significant.

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