Suppr超能文献

钙和整合素结合蛋白 1 调节巨核细胞的倍性、黏附和迁移。

Calcium- and integrin-binding protein 1 regulates megakaryocyte ploidy, adhesion, and migration.

机构信息

Department of Biological Sciences, University of Delaware, Newark, USA.

出版信息

Blood. 2012 Jan 19;119(3):838-46. doi: 10.1182/blood-2011-04-346098. Epub 2011 Nov 29.

Abstract

Megakaryocytes are large, polyploid cells that produce platelets. We have previously reported that calcium- and integrin-binding protein 1 (CIB1) regulates endomitosis in Dami cells. To further characterize the role of CIB1 in megakaryopoiesis, we used a Cib1(-/-) mouse model. Cib1(-/-) mice have more platelets and BM megakaryocytes than wild-type (WT) controls (P < .05). Furthermore, subsequent analysis of megakaryocyte-CFU production revealed an increase with Cib1 deletion compared with WT (P < .05). In addition, BM from Cib1(-/-) mice, cultured with thrombopoietin (TPO) for 24 hours, produced more highly polyploid megakaryocytes than WT BM (P < .05). Subsequent analysis of TPO signaling revealed enhanced Akt and ERK1/2 phosphorylation, whereas FAK(Y925) phosphorylation was reduced in Cib1(-/-) megakaryocytes treated with TPO. Conversely, platelet recovery in Cib1(-/-) mice after platelet depletion was attenuated compared with WT (P < .05). This could be the result of impaired adhesion and migration, as adhesion to fibrinogen and fibronectin and migration toward an SDF-1α gradient were reduced in Cib1(-/-) megakaryocytes compared with WT (P < .05). In addition, Cib1(-/-) megakaryocytes formed fewer proplatelets compared with WT (P < .05), when plated on fibrinogen. These data suggest that CIB1 plays a dual role in megakaryopoiesis, initially by negatively regulating TPO signaling and later by augmenting proplatelet production.

摘要

巨核细胞是产生血小板的大型多倍体细胞。我们之前报道过钙和整合素结合蛋白 1(CIB1)调节 Dami 细胞的核内有丝分裂。为了进一步表征 CIB1 在巨核细胞生成中的作用,我们使用了 Cib1(-/-)小鼠模型。Cib1(-/-)小鼠的血小板和 BM 巨核细胞比野生型(WT)对照多(P <.05)。此外,随后对巨核细胞集落形成单位(CFU)的分析显示,与 WT 相比,Cib1 缺失导致 CFU 增加(P <.05)。此外,用血小板生成素(TPO)培养 24 小时后,Cib1(-/-)小鼠的 BM 产生的高度多倍体巨核细胞比 WT BM 多(P <.05)。随后对 TPO 信号的分析显示,Akt 和 ERK1/2 的磷酸化增强,而 Cib1(-/-)巨核细胞中 TPO 处理后 FAK(Y925)的磷酸化减少。相反,与 WT 相比,Cib1(-/-)小鼠在血小板耗竭后血小板恢复减弱(P <.05)。这可能是由于粘附和迁移受损所致,因为与 WT 相比,Cib1(-/-)巨核细胞对纤维蛋白原和纤维连接蛋白的粘附以及向 SDF-1α 梯度的迁移减少(P <.05)。此外,与 WT 相比,Cib1(-/-)巨核细胞在纤维蛋白原上形成的原血小板较少(P <.05)。这些数据表明,CIB1 在巨核细胞生成中发挥双重作用,最初通过负调控 TPO 信号,然后通过增强原血小板生成。

相似文献

引用本文的文献

1
Discovery and Development of Cyclic Peptide Inhibitors of CIB1.CIB1环肽抑制剂的发现与开发
ACS Med Chem Lett. 2021 Oct 27;12(11):1832-1839. doi: 10.1021/acsmedchemlett.1c00438. eCollection 2021 Nov 11.
7
CIB1: a small protein with big ambitions.CIB1:一个抱负远大的小蛋白。
FASEB J. 2016 Aug;30(8):2640-50. doi: 10.1096/fj.201500073R. Epub 2016 Apr 26.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验