Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia

Immune thrombocytopenia (ITP) is a common acquired autoimmune disease, and thrombopoietin (TPO) is an important cytokine that regulates the production of megakaryocytes and platelets. We have identified a biologically active component, icaritin, from a Chinese herba epimedii extract. Icaritin promot...

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Main Authors: Ke Zhang, Zhenfeng Dai, Runzhe Liu, Fang Tian, Xi Liu, Yi Sun, Xin Zhao, Xiaoping Pu
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:Mediators of Inflammation
Online Access:http://dx.doi.org/10.1155/2018/7235639
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author Ke Zhang
Zhenfeng Dai
Runzhe Liu
Fang Tian
Xi Liu
Yi Sun
Xin Zhao
Xiaoping Pu
author_facet Ke Zhang
Zhenfeng Dai
Runzhe Liu
Fang Tian
Xi Liu
Yi Sun
Xin Zhao
Xiaoping Pu
author_sort Ke Zhang
collection DOAJ
description Immune thrombocytopenia (ITP) is a common acquired autoimmune disease, and thrombopoietin (TPO) is an important cytokine that regulates the production of megakaryocytes and platelets. We have identified a biologically active component, icaritin, from a Chinese herba epimedii extract. Icaritin promotes platelet production and regulates T cell polarization, but its mechanism is not clear. In this study, the BALB/c mouse model of ITP was established by injection of an antiplatelet antibody every other day for seven total times. The antiplatelet sera were derived from guinea pigs immunized with the platelets of BALB/c mice. Mice with ITP were treated with icaritin at low, moderate, or high doses of 4.73, 9.45, and 18.90 mg/kg, respectively, for fourteen consecutive days. The present study shows that icaritin can significantly increase peripheral blood platelet counts and thrombocytocrit, increase the TPO level in serum, attenuate splenomegaly, and reduce the abnormal proliferation of megakaryocytes in the spleen and bone marrow. Icaritin can also downregulate the expression of bone marrow TPO, myeloproliferative leukemia virus oncogene (MPL), and p-Stat3. Our results suggest that icaritin can significantly improve the health of mice with ITP via possible downregulation of p-Stat3 expression in the JAK2/Stat3 phosphorylation signaling pathway and regulation of bone marrow TPO/MPL metabolism.
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spelling doaj-art-58cb5272ee4f48b7810d07d25bdb686b2025-02-03T01:24:24ZengWileyMediators of Inflammation0962-93511466-18612018-01-01201810.1155/2018/72356397235639Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune ThrombocytopeniaKe Zhang0Zhenfeng Dai1Runzhe Liu2Fang Tian3Xi Liu4Yi Sun5Xin Zhao6Xiaoping Pu7National Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaNational Key Research Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, ChinaImmune thrombocytopenia (ITP) is a common acquired autoimmune disease, and thrombopoietin (TPO) is an important cytokine that regulates the production of megakaryocytes and platelets. We have identified a biologically active component, icaritin, from a Chinese herba epimedii extract. Icaritin promotes platelet production and regulates T cell polarization, but its mechanism is not clear. In this study, the BALB/c mouse model of ITP was established by injection of an antiplatelet antibody every other day for seven total times. The antiplatelet sera were derived from guinea pigs immunized with the platelets of BALB/c mice. Mice with ITP were treated with icaritin at low, moderate, or high doses of 4.73, 9.45, and 18.90 mg/kg, respectively, for fourteen consecutive days. The present study shows that icaritin can significantly increase peripheral blood platelet counts and thrombocytocrit, increase the TPO level in serum, attenuate splenomegaly, and reduce the abnormal proliferation of megakaryocytes in the spleen and bone marrow. Icaritin can also downregulate the expression of bone marrow TPO, myeloproliferative leukemia virus oncogene (MPL), and p-Stat3. Our results suggest that icaritin can significantly improve the health of mice with ITP via possible downregulation of p-Stat3 expression in the JAK2/Stat3 phosphorylation signaling pathway and regulation of bone marrow TPO/MPL metabolism.http://dx.doi.org/10.1155/2018/7235639
spellingShingle Ke Zhang
Zhenfeng Dai
Runzhe Liu
Fang Tian
Xi Liu
Yi Sun
Xin Zhao
Xiaoping Pu
Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
Mediators of Inflammation
title Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
title_full Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
title_fullStr Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
title_full_unstemmed Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
title_short Icaritin Provokes Serum Thrombopoietin and Downregulates Thrombopoietin/MPL of the Bone Marrow in a Mouse Model of Immune Thrombocytopenia
title_sort icaritin provokes serum thrombopoietin and downregulates thrombopoietin mpl of the bone marrow in a mouse model of immune thrombocytopenia
url http://dx.doi.org/10.1155/2018/7235639
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