PDPN/CLEC-2轴以造血干细胞调控巨核细胞显性方式调节巨核细胞亚型

IF 3.7 3区 医学 Q1 HEMATOLOGY
Rikuto Nara , Hinako Notoh , Tomoyuki Sasaki , Nagaharu Tsukiji , Toshiaki Shirai , Ayuka Kamata , Nobuaki Suzuki , Atsuo Suzuki , Shuichi Okamoto , Takeshi Kanematsu , Naruko Suzuki , Akira Katsumi , Tetsuhito Kojima , Katsue Suzuki-Inoue , Tadashi Matsushita , Shogo Tamura
{"title":"PDPN/CLEC-2轴以造血干细胞调控巨核细胞显性方式调节巨核细胞亚型","authors":"Rikuto Nara ,&nbsp;Hinako Notoh ,&nbsp;Tomoyuki Sasaki ,&nbsp;Nagaharu Tsukiji ,&nbsp;Toshiaki Shirai ,&nbsp;Ayuka Kamata ,&nbsp;Nobuaki Suzuki ,&nbsp;Atsuo Suzuki ,&nbsp;Shuichi Okamoto ,&nbsp;Takeshi Kanematsu ,&nbsp;Naruko Suzuki ,&nbsp;Akira Katsumi ,&nbsp;Tetsuhito Kojima ,&nbsp;Katsue Suzuki-Inoue ,&nbsp;Tadashi Matsushita ,&nbsp;Shogo Tamura","doi":"10.1016/j.thromres.2024.109230","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Megakaryocytes are classified into several subtypes including LSP1-positive immune-skewed, MYLK4-positive hematopoietic stem cell (HSC)-regulating, and BMAL1-positive platelet-producing megakaryocytes. Podoplanin (PDPN)-expressing stromal cells generate a microenvironment that promotes megakaryopoiesis in the bone marrow. In this context, PDPN interacts with C-type lectin-like receptor-2 (CLEC-2) on megakaryocyte progenitors, which induces megakaryocyte proliferation. However, the megakaryocyte subtypes developed by the regulation of the PDPN/CLEC-2 axis have not yet been elucidated.</div></div><div><h3>Materials and methods</h3><div>We established an immortalized bone marrow PDPN-expressing stromal cell line and a PDPN-knockout line (PDPN WT and KO feeder cells, respectively). Bone marrow hematopoietic progenitors were committed to megakaryocytes in co-culture with PDPN WT or KO feeder cells. The number and ploidy of megakaryocytes, resultant platelets, and the polarization of megakaryocyte subtypes were investigated.</div></div><div><h3>Results</h3><div>The number of megakaryocytes was significantly increased in the co-culture with PDPN WT feeder cells compared to that with PDPN KO feeder cells. The megakaryocytes on the PDPN WT and KO feeders showed their main ploidy at 16 N∼32 N and 8 N∼16 N, respectively. The number of platelets was decreased in the co-culture with the PDPN WT feeder compared to that in the co-culture with the PDPN KO feeder. For each megakaryocyte subtype, the percentage of MYLK4-positive megakaryocytes significantly increased and the percentage of BMAL1-positive megakaryocytes significantly decreased when co-cultured with the PDPN WT feeder. These results were also confirmed in the co-culture of CLEC-2 conditional KO megakaryocytes with PDPN WT feeder cells.</div></div><div><h3>Conclusion</h3><div>The PDPN/CLEC-2 axis modulates megakaryocyte subtype differentiation, with a predominance of HSC-regulating megakaryocytes.</div></div>","PeriodicalId":23064,"journal":{"name":"Thrombosis research","volume":"245 ","pages":"Article 109230"},"PeriodicalIF":3.7000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PDPN/CLEC-2 axis modulates megakaryocyte subtypes in a hematopoietic stem cell-regulating megakaryocyte-dominant manner\",\"authors\":\"Rikuto Nara ,&nbsp;Hinako Notoh ,&nbsp;Tomoyuki Sasaki ,&nbsp;Nagaharu Tsukiji ,&nbsp;Toshiaki Shirai ,&nbsp;Ayuka Kamata ,&nbsp;Nobuaki Suzuki ,&nbsp;Atsuo Suzuki ,&nbsp;Shuichi Okamoto ,&nbsp;Takeshi Kanematsu ,&nbsp;Naruko Suzuki ,&nbsp;Akira Katsumi ,&nbsp;Tetsuhito Kojima ,&nbsp;Katsue Suzuki-Inoue ,&nbsp;Tadashi Matsushita ,&nbsp;Shogo Tamura\",\"doi\":\"10.1016/j.thromres.2024.109230\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><div>Megakaryocytes are classified into several subtypes including LSP1-positive immune-skewed, MYLK4-positive hematopoietic stem cell (HSC)-regulating, and BMAL1-positive platelet-producing megakaryocytes. Podoplanin (PDPN)-expressing stromal cells generate a microenvironment that promotes megakaryopoiesis in the bone marrow. In this context, PDPN interacts with C-type lectin-like receptor-2 (CLEC-2) on megakaryocyte progenitors, which induces megakaryocyte proliferation. However, the megakaryocyte subtypes developed by the regulation of the PDPN/CLEC-2 axis have not yet been elucidated.</div></div><div><h3>Materials and methods</h3><div>We established an immortalized bone marrow PDPN-expressing stromal cell line and a PDPN-knockout line (PDPN WT and KO feeder cells, respectively). Bone marrow hematopoietic progenitors were committed to megakaryocytes in co-culture with PDPN WT or KO feeder cells. The number and ploidy of megakaryocytes, resultant platelets, and the polarization of megakaryocyte subtypes were investigated.</div></div><div><h3>Results</h3><div>The number of megakaryocytes was significantly increased in the co-culture with PDPN WT feeder cells compared to that with PDPN KO feeder cells. The megakaryocytes on the PDPN WT and KO feeders showed their main ploidy at 16 N∼32 N and 8 N∼16 N, respectively. The number of platelets was decreased in the co-culture with the PDPN WT feeder compared to that in the co-culture with the PDPN KO feeder. For each megakaryocyte subtype, the percentage of MYLK4-positive megakaryocytes significantly increased and the percentage of BMAL1-positive megakaryocytes significantly decreased when co-cultured with the PDPN WT feeder. These results were also confirmed in the co-culture of CLEC-2 conditional KO megakaryocytes with PDPN WT feeder cells.</div></div><div><h3>Conclusion</h3><div>The PDPN/CLEC-2 axis modulates megakaryocyte subtype differentiation, with a predominance of HSC-regulating megakaryocytes.</div></div>\",\"PeriodicalId\":23064,\"journal\":{\"name\":\"Thrombosis research\",\"volume\":\"245 \",\"pages\":\"Article 109230\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2024-11-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Thrombosis research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0049384824003621\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Thrombosis research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0049384824003621","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

巨核细胞分为几种亚型,包括lsp1阳性免疫偏斜型、mylk4阳性造血干细胞(HSC)调节型和bmal1阳性血小板生成型巨核细胞。表达Podoplanin (PDPN)的基质细胞产生促进骨髓巨核生成的微环境。在这种情况下,PDPN与巨核细胞祖细胞上的c型凝集素样受体-2 (clc -2)相互作用,诱导巨核细胞增殖。然而,通过调控PDPN/CLEC-2轴而形成的巨核细胞亚型尚未被阐明。材料与方法建立永生化骨髓PDPN表达基质细胞系和PDPN敲除细胞系(分别为PDPN WT和KO饲养细胞)。骨髓造血祖细胞与PDPN、WT或KO饲养细胞共培养,形成巨核细胞。研究了巨核细胞的数量和倍性,由此产生的血小板,以及巨核细胞亚型的极化。结果与PDPN WT饲养细胞共培养,巨核细胞数量明显高于与PDPN KO饲养细胞共培养。PDPN WT和KO饲料上的巨核细胞分别在16 N ~ 32 N和8 N ~ 16 N时显示出其主要倍性。与与PDPN KO饲料共培养相比,与PDPN WT饲料共培养的血小板数量减少。对于每种巨核细胞亚型,与PDPN WT饲养器共培养时,mylk4阳性巨核细胞百分比显著增加,bmal1阳性巨核细胞百分比显著降低。这些结果也在clc -2条件KO巨核细胞与PDPN WT饲养细胞共培养中得到证实。结论PDPN/CLEC-2轴调控巨核细胞亚型分化,以hsc调控巨核细胞为主。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PDPN/CLEC-2 axis modulates megakaryocyte subtypes in a hematopoietic stem cell-regulating megakaryocyte-dominant manner

Introduction

Megakaryocytes are classified into several subtypes including LSP1-positive immune-skewed, MYLK4-positive hematopoietic stem cell (HSC)-regulating, and BMAL1-positive platelet-producing megakaryocytes. Podoplanin (PDPN)-expressing stromal cells generate a microenvironment that promotes megakaryopoiesis in the bone marrow. In this context, PDPN interacts with C-type lectin-like receptor-2 (CLEC-2) on megakaryocyte progenitors, which induces megakaryocyte proliferation. However, the megakaryocyte subtypes developed by the regulation of the PDPN/CLEC-2 axis have not yet been elucidated.

Materials and methods

We established an immortalized bone marrow PDPN-expressing stromal cell line and a PDPN-knockout line (PDPN WT and KO feeder cells, respectively). Bone marrow hematopoietic progenitors were committed to megakaryocytes in co-culture with PDPN WT or KO feeder cells. The number and ploidy of megakaryocytes, resultant platelets, and the polarization of megakaryocyte subtypes were investigated.

Results

The number of megakaryocytes was significantly increased in the co-culture with PDPN WT feeder cells compared to that with PDPN KO feeder cells. The megakaryocytes on the PDPN WT and KO feeders showed their main ploidy at 16 N∼32 N and 8 N∼16 N, respectively. The number of platelets was decreased in the co-culture with the PDPN WT feeder compared to that in the co-culture with the PDPN KO feeder. For each megakaryocyte subtype, the percentage of MYLK4-positive megakaryocytes significantly increased and the percentage of BMAL1-positive megakaryocytes significantly decreased when co-cultured with the PDPN WT feeder. These results were also confirmed in the co-culture of CLEC-2 conditional KO megakaryocytes with PDPN WT feeder cells.

Conclusion

The PDPN/CLEC-2 axis modulates megakaryocyte subtype differentiation, with a predominance of HSC-regulating megakaryocytes.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Thrombosis research
Thrombosis research 医学-外周血管病
CiteScore
14.60
自引率
4.00%
发文量
364
审稿时长
31 days
期刊介绍: Thrombosis Research is an international journal dedicated to the swift dissemination of new information on thrombosis, hemostasis, and vascular biology, aimed at advancing both science and clinical care. The journal publishes peer-reviewed original research, reviews, editorials, opinions, and critiques, covering both basic and clinical studies. Priority is given to research that promises novel approaches in the diagnosis, therapy, prognosis, and prevention of thrombotic and hemorrhagic diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信