临床输血与检验 ›› 2025, Vol. 27 ›› Issue (2): 234-246.DOI: 10.3969/j.issn.1671-2587.2025.02.014
赖冬娣1,2,3, 钟明璐1,2,3, 董涵1,2, 彭伟康1,2,3, 魏亚明1,2,3, 苑召虎1,2,3
收稿日期:
2024-12-23
出版日期:
2025-04-20
发布日期:
2025-04-17
通讯作者:
苑召虎,主要从事输血免疫学研究,(E-mail)eyyuanzhaohu@scut.edu.cn。共同通信作者:魏亚明,主要从事输血治疗相关研究,(E-mail)eywym@scut.edu.cn。
作者简介:
赖冬娣,主要从事输血治疗和输血医学免疫学研究,(E-mail)1337151807@qq.com。
基金资助:
LAI Dongdi1,2,3, ZHONG Minglu1,2,3, DONG Han1,2, PENG Weikang1,2,3, WEI Yaming1,2,3, YUAN Zhaohu1,2,3
Received:
2024-12-23
Online:
2025-04-20
Published:
2025-04-17
摘要: 信号素家族成员Sema7a,也称为CDw108、JMH抗原,是一种糖基磷脂酰肌醇(glycosylphosphatidylinositol, GPI)锚定的糖蛋白,广泛表达在全身多种组织细胞膜上。Sema7a蛋白可以受酶、血液应切力、缺氧等多种物理化学因素影响,从细胞膜上裂解下来,其中来源于红细胞膜表面的Sema7a蛋白是体内游离Sema7a的主要来源。Sema7a蛋白与两种已知的受体——整合素和丛蛋白C1(Plexin C1)结合或以游离方式参与全身多种生物活动过程,在细胞分化、神经信号转导、免疫应答、炎症调节及肿瘤进展等方面具有重要作用。本文根据系统疾病分类,对Sema7a蛋白参与不同疾病发生、发展的机制进行了叙述和总结。
中图分类号:
赖冬娣, 钟明璐, 董涵, 彭伟康, 魏亚明, 苑召虎. Sema7a蛋白作用机制研究进展*[J]. 临床输血与检验, 2025, 27(2): 234-246.
LAI Dongdi, ZHONG Minglu, DONG Han, PENG Weikang, WEI Yaming, YUAN Zhaohu. New Progress on the Molecular Mechanism of Sema7a Protein[J]. JOURNAL OF CLINICAL TRANSFUSION AND LABORATORY MEDICINE, 2025, 27(2): 234-246.
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Sema7a促进内皮细胞与巨核细胞粘附的机制研究[J]. 临床输血与检验,2024, 26(3):299-308. |
[1] | 赖冬娣, 董涵, 魏亚明, 苑召虎. Sema7a促进内皮细胞与巨核细胞粘附的机制研究*[J]. 临床输血与检验, 2024, 26(3): 299-308. |
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