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PDPN/CLEC-2轴以造血干细胞调节巨核细胞为主导的方式调节巨核细胞亚型。

PDPN/CLEC-2 axis modulates megakaryocyte subtypes in a hematopoietic stem cell-regulating megakaryocyte-dominant manner.

作者信息

Nara Rikuto, Notoh Hinako, Sasaki Tomoyuki, Tsukiji Nagaharu, Shirai Toshiaki, Kamata Ayuka, Suzuki Nobuaki, Suzuki Atsuo, Okamoto Shuichi, Kanematsu Takeshi, Suzuki Naruko, Katsumi Akira, Kojima Tetsuhito, Suzuki-Inoue Katsue, Matsushita Tadashi, Tamura Shogo

机构信息

Graduate School of Health Sciences, Hokkaido University, Japan.

Department of Clinical and Laboratory Medicine, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan.

出版信息

Thromb Res. 2025 Jan;245:109230. doi: 10.1016/j.thromres.2024.109230. Epub 2024 Nov 26.

Abstract

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.

摘要

引言

巨核细胞可分为几种亚型,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。表达血小板内皮细胞黏附分子(PDPN)的基质细胞产生促进骨髓中巨核细胞生成的微环境。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(CLEC-2)相互作用,诱导巨核细胞增殖。然而,由PDPN/CLEC-2轴调控产生的巨核细胞亚型尚未阐明。

材料与方法

我们建立了永生化的表达骨髓PDPN的基质细胞系和PDPN基因敲除系(分别为PDPN野生型和敲除型饲养细胞)。骨髓造血祖细胞与PDPN野生型或敲除型饲养细胞共培养,定向分化为巨核细胞。研究了巨核细胞的数量和倍性、产生的血小板以及巨核细胞亚型的极化情况。

结果

与PDPN敲除型饲养细胞共培养相比,与PDPN野生型饲养细胞共培养时巨核细胞数量显著增加。PDPN野生型和敲除型饲养细胞上的巨核细胞主要倍性分别为16N至32N和8N至16N。与PDPN敲除型饲养细胞共培养相比,与PDPN野生型饲养细胞共培养时血小板数量减少。对于每种巨核细胞亚型,与PDPN野生型饲养细胞共培养时,MYLK4阳性巨核细胞的百分比显著增加,而BMAL1阳性巨核细胞的百分比显著降低。在CLEC-2条件性敲除巨核细胞与PDPN野生型饲养细胞的共培养中也证实了这些结果。

结论

PDPN/CLEC-2轴调节巨核细胞亚型分化,以HSC调节型巨核细胞为主。

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