Fig. 4From: Angptl4 is upregulated under inflammatory conditions in the bone marrow of mice, expands myeloid progenitors, and accelerates reconstitution of platelets after myelosuppressive therapyIn vivo treatment with Angptl4 increases immature megakaryocytes and results in elevated platelet counts. a Hematoxylin-eosin staining of BM sections from PBS- or Angptl4-treated WT mice. Mice were daily injected with 250 μg/kg murine Angptl4 per kg body weight for five consecutive days and analyzed 48 h after the last injection. The symbol “x” indicates MKs in the BM of PBS- and rmAngptl-treated mice, and arrows indicate immature MKs in the BM of Angptl4-injected animals. One representative analysis from three independent experiments is shown. Magnification ×200. b Representative FACS profile of Lin− BM cells from PBS- and Angptl4-injected WT mice. Lin−CD45+CD61+ cells were subdivided into three subsets based on CD61 and CD41 expression: CD61+, CD61+CD41high, and CD61+CD41low cells. c Frequency and total cell numbers/tibia of CD61+, CD61+CD41high, and CD61+CD41low cells. Mean ± SEM of three different experiments with three PBS-injected and three Angptl4-injected mice/group are shown. d PLT counts from PBS- or Angptl4-treated WT mice. Mean ± SEM of three different experiments with three PBS-injected and three Angptl4-injected mice/group are shown. Statistically significant differences are indicated (**p < 0.01)Back to article page