Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling

Abstract The supply of platelets for clinical transfusion is often insufficient to meet growing demand. Platelet regeneration from stem cells offers a potential solution to reduce reliance on donor‐based transfusions. However, the current differentiation efficiency is suboptimal. A novel approach is...

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Main Authors: Huicong Liu, Lingna Wang, Jiaqing Liu, Haitao Yuan, Kaiqing Zhang, Yun Qiu, Fangfang Zhu
Format: Article
Language:English
Published: Wiley 2025-06-01
Series:Advanced Science
Subjects:
Online Access:https://doi.org/10.1002/advs.202500612
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author Huicong Liu
Lingna Wang
Jiaqing Liu
Haitao Yuan
Kaiqing Zhang
Yun Qiu
Fangfang Zhu
author_facet Huicong Liu
Lingna Wang
Jiaqing Liu
Haitao Yuan
Kaiqing Zhang
Yun Qiu
Fangfang Zhu
author_sort Huicong Liu
collection DOAJ
description Abstract The supply of platelets for clinical transfusion is often insufficient to meet growing demand. Platelet regeneration from stem cells offers a potential solution to reduce reliance on donor‐based transfusions. However, the current differentiation efficiency is suboptimal. A novel approach is presented that significantly enhances platelet yield from hematopoietic stem and progenitor cells (HSPCs) by increasing the production of megakaryocyte progenitors (MkPs) and mature megakaryocytes (MKs). This method employs the overexpression of HES7 combined with the HDAC inhibitor and GABA agonist (collectively termed the VGM cocktail). The VGM cocktail induces MkP production with an efficiency of up to 90%, validated across HSPCs from various donors. These MkPs exhibit extended proliferative capacity, remaining viable for up to 51 days in prolonged culture, and show enhanced maturation into MKs. This differentiation system effectively replicates in vivo thrombocytopoiesis, as evidenced by polyploidization, long protrusions, and proplatelet formation. Transfusion of VGM‐induced MkPs into thrombocytopenic mice results in the release of platelets into circulation. Mechanistic investigation identifies the JAK2/STAT3 signaling pathway as critical in promoting megakaryopoiesis within this system. Therefore, this study demonstrates that the VGM cocktail facilitates enhanced platelet production by promoting MkP generation, offering a promising strategy for in vitro platelet regeneration for clinical applications.
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spelling doaj-art-a22dd87ac5da474cb74f48e71686a63a2025-08-20T03:31:26ZengWileyAdvanced Science2198-38442025-06-011223n/an/a10.1002/advs.202500612Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 SignalingHuicong Liu0Lingna Wang1Jiaqing Liu2Haitao Yuan3Kaiqing Zhang4Yun Qiu5Fangfang Zhu6School of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaSchool of Biomedical Engineering Shanghai Jiao Tong University Shanghai 200030 ChinaAbstract The supply of platelets for clinical transfusion is often insufficient to meet growing demand. Platelet regeneration from stem cells offers a potential solution to reduce reliance on donor‐based transfusions. However, the current differentiation efficiency is suboptimal. A novel approach is presented that significantly enhances platelet yield from hematopoietic stem and progenitor cells (HSPCs) by increasing the production of megakaryocyte progenitors (MkPs) and mature megakaryocytes (MKs). This method employs the overexpression of HES7 combined with the HDAC inhibitor and GABA agonist (collectively termed the VGM cocktail). The VGM cocktail induces MkP production with an efficiency of up to 90%, validated across HSPCs from various donors. These MkPs exhibit extended proliferative capacity, remaining viable for up to 51 days in prolonged culture, and show enhanced maturation into MKs. This differentiation system effectively replicates in vivo thrombocytopoiesis, as evidenced by polyploidization, long protrusions, and proplatelet formation. Transfusion of VGM‐induced MkPs into thrombocytopenic mice results in the release of platelets into circulation. Mechanistic investigation identifies the JAK2/STAT3 signaling pathway as critical in promoting megakaryopoiesis within this system. Therefore, this study demonstrates that the VGM cocktail facilitates enhanced platelet production by promoting MkP generation, offering a promising strategy for in vitro platelet regeneration for clinical applications.https://doi.org/10.1002/advs.202500612GABAHDACHES7JAK/STATmegakaryocyte progenitorplatelet
spellingShingle Huicong Liu
Lingna Wang
Jiaqing Liu
Haitao Yuan
Kaiqing Zhang
Yun Qiu
Fangfang Zhu
Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
Advanced Science
GABA
HDAC
HES7
JAK/STAT
megakaryocyte progenitor
platelet
title Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
title_full Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
title_fullStr Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
title_full_unstemmed Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
title_short Efficient Generation of Megakaryocyte Progenitors and Platelets From HSPCs via JAK2/STAT3 Signaling
title_sort efficient generation of megakaryocyte progenitors and platelets from hspcs via jak2 stat3 signaling
topic GABA
HDAC
HES7
JAK/STAT
megakaryocyte progenitor
platelet
url https://doi.org/10.1002/advs.202500612
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