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Hyperhomocysteinemia potentiates megakaryocyte differentiation and thrombopoiesis via GH-PI3K-Akt axis

Hyperhomocysteinemia (HHcy) is closely associated with thrombotic diseases such as myocardial infarction and stroke. Enhanced platelet activation was observed in animals and humans with HHcy. However, the influence of HHcy on thrombopoiesis remains largely unknown. Here, we reported increased platel...

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Published in:Journal of hematology and oncology 2023-07, Vol.16 (1), p.84-84, Article 84
Main Authors: Lei, Wenjing, Liu, Zhuoliang, Su, Zhiyuan, Meng, Panpan, Zhou, Chun, Chen, Xiaomei, Hu, Zheng, Xiao, An, Zhou, Miaomiao, Huang, Liping, Zhang, Yiyue, Qin, Xianhui, Wang, Junping, Zhu, Fengxin, Nie, Jing
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container_title Journal of hematology and oncology
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creator Lei, Wenjing
Liu, Zhuoliang
Su, Zhiyuan
Meng, Panpan
Zhou, Chun
Chen, Xiaomei
Hu, Zheng
Xiao, An
Zhou, Miaomiao
Huang, Liping
Zhang, Yiyue
Qin, Xianhui
Wang, Junping
Zhu, Fengxin
Nie, Jing
description Hyperhomocysteinemia (HHcy) is closely associated with thrombotic diseases such as myocardial infarction and stroke. Enhanced platelet activation was observed in animals and humans with HHcy. However, the influence of HHcy on thrombopoiesis remains largely unknown. Here, we reported increased platelet count (PLT) in mice and zebrafish with HHcy. In hypertensive patients (n = 11,189), higher serum level of total Hcy was observed in participants with PLT ≥ 291 × 10 /L (full adjusted β, 0.59; 95% CI 0.14, 1.04). We used single-cell RNA sequencing (scRNA-seq) to characterize the impact of Hcy on transcriptome, cellular heterogeneity, and developmental trajectories of megakaryopoiesis from human umbilical cord blood (hUCB) CD34 cells. Together with in vitro and in vivo analysis, we demonstrated that Hcy promoted megakaryocytes (MKs) differentiation via growth hormone (GH)-PI3K-Akt axis. Moreover, the effect of Hcy on thrombopoiesis is independent of thrombopoietin (TPO) because administration of Hcy also led to a significant increase of PLT in homozygous TPO receptor (Mpl) mutant mice and zebrafish. Administration of melatonin effectively reversed Hcy-induced thrombopoiesis in mice. ScRNA-seq showed that melatonin abolished Hcy-facilitated MK differentiation and maturation, inhibited the activation of GH-PI3K-Akt signaling. Our work reveals a previously unrecognized role of HHcy in thrombopoiesis and provides new insight into the mechanisms by which HHcy confers an increased thrombotic risk.Trial Registration clinicaltrials.gov Identifier: NCT00794885.
doi_str_mv 10.1186/s13045-023-01481-x
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Enhanced platelet activation was observed in animals and humans with HHcy. However, the influence of HHcy on thrombopoiesis remains largely unknown. Here, we reported increased platelet count (PLT) in mice and zebrafish with HHcy. In hypertensive patients (n = 11,189), higher serum level of total Hcy was observed in participants with PLT ≥ 291 × 10 /L (full adjusted β, 0.59; 95% CI 0.14, 1.04). We used single-cell RNA sequencing (scRNA-seq) to characterize the impact of Hcy on transcriptome, cellular heterogeneity, and developmental trajectories of megakaryopoiesis from human umbilical cord blood (hUCB) CD34 cells. Together with in vitro and in vivo analysis, we demonstrated that Hcy promoted megakaryocytes (MKs) differentiation via growth hormone (GH)-PI3K-Akt axis. Moreover, the effect of Hcy on thrombopoiesis is independent of thrombopoietin (TPO) because administration of Hcy also led to a significant increase of PLT in homozygous TPO receptor (Mpl) mutant mice and zebrafish. Administration of melatonin effectively reversed Hcy-induced thrombopoiesis in mice. ScRNA-seq showed that melatonin abolished Hcy-facilitated MK differentiation and maturation, inhibited the activation of GH-PI3K-Akt signaling. Our work reveals a previously unrecognized role of HHcy in thrombopoiesis and provides new insight into the mechanisms by which HHcy confers an increased thrombotic risk.Trial Registration clinicaltrials.gov Identifier: NCT00794885.</description><identifier>ISSN: 1756-8722</identifier><identifier>EISSN: 1756-8722</identifier><identifier>DOI: 10.1186/s13045-023-01481-x</identifier><identifier>PMID: 37501059</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>1-Phosphatidylinositol 3-kinase ; AKT protein ; Animals ; Blood Platelets ; Bone marrow ; CD34 antigen ; Cell Differentiation ; Cerebral infarction ; Cord blood ; Correspondence ; Danio rerio ; Disease prevention ; Genes ; Growth hormone ; Growth Hormone - pharmacology ; Growth hormones ; Heart attack ; Hematology ; Homocysteine ; Humans ; Hyperhomocysteinemia ; Hyperhomocysteinemia - complications ; Hypertension ; Kinases ; Megakaryocyte ; Megakaryocytes ; Melatonin ; Melatonin - pharmacology ; Mice ; Mutation ; Myocardial infarction ; Oncology ; Ontology ; Phosphatidylinositol 3-Kinases ; Platelets ; Proto-Oncogene Proteins c-akt - genetics ; RNA sequencing ; ScRNA-seq ; Somatotropin ; Stroke ; Thromboembolism ; Thrombopoiesis ; Thrombopoiesis - genetics ; Thrombopoietin ; Thrombosis ; Transcriptomes ; Umbilical cord ; Zebrafish</subject><ispartof>Journal of hematology and oncology, 2023-07, Vol.16 (1), p.84-84, Article 84</ispartof><rights>2023. 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Administration of melatonin effectively reversed Hcy-induced thrombopoiesis in mice. ScRNA-seq showed that melatonin abolished Hcy-facilitated MK differentiation and maturation, inhibited the activation of GH-PI3K-Akt signaling. 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Enhanced platelet activation was observed in animals and humans with HHcy. However, the influence of HHcy on thrombopoiesis remains largely unknown. Here, we reported increased platelet count (PLT) in mice and zebrafish with HHcy. In hypertensive patients (n = 11,189), higher serum level of total Hcy was observed in participants with PLT ≥ 291 × 10 /L (full adjusted β, 0.59; 95% CI 0.14, 1.04). We used single-cell RNA sequencing (scRNA-seq) to characterize the impact of Hcy on transcriptome, cellular heterogeneity, and developmental trajectories of megakaryopoiesis from human umbilical cord blood (hUCB) CD34 cells. Together with in vitro and in vivo analysis, we demonstrated that Hcy promoted megakaryocytes (MKs) differentiation via growth hormone (GH)-PI3K-Akt axis. Moreover, the effect of Hcy on thrombopoiesis is independent of thrombopoietin (TPO) because administration of Hcy also led to a significant increase of PLT in homozygous TPO receptor (Mpl) mutant mice and zebrafish. Administration of melatonin effectively reversed Hcy-induced thrombopoiesis in mice. ScRNA-seq showed that melatonin abolished Hcy-facilitated MK differentiation and maturation, inhibited the activation of GH-PI3K-Akt signaling. Our work reveals a previously unrecognized role of HHcy in thrombopoiesis and provides new insight into the mechanisms by which HHcy confers an increased thrombotic risk.Trial Registration clinicaltrials.gov Identifier: NCT00794885.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>37501059</pmid><doi>10.1186/s13045-023-01481-x</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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ispartof Journal of hematology and oncology, 2023-07, Vol.16 (1), p.84-84, Article 84
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1756-8722
language eng
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subjects 1-Phosphatidylinositol 3-kinase
AKT protein
Animals
Blood Platelets
Bone marrow
CD34 antigen
Cell Differentiation
Cerebral infarction
Cord blood
Correspondence
Danio rerio
Disease prevention
Genes
Growth hormone
Growth Hormone - pharmacology
Growth hormones
Heart attack
Hematology
Homocysteine
Humans
Hyperhomocysteinemia
Hyperhomocysteinemia - complications
Hypertension
Kinases
Megakaryocyte
Megakaryocytes
Melatonin
Melatonin - pharmacology
Mice
Mutation
Myocardial infarction
Oncology
Ontology
Phosphatidylinositol 3-Kinases
Platelets
Proto-Oncogene Proteins c-akt - genetics
RNA sequencing
ScRNA-seq
Somatotropin
Stroke
Thromboembolism
Thrombopoiesis
Thrombopoiesis - genetics
Thrombopoietin
Thrombosis
Transcriptomes
Umbilical cord
Zebrafish
title Hyperhomocysteinemia potentiates megakaryocyte differentiation and thrombopoiesis via GH-PI3K-Akt axis
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