Ghasempour Sina, Muise Aleixo M, Freeman Spencer A
Program in Cell Biology, Peter Gilgan Centre for Research and Learning, Hospital for Sick Children, Toronto, Ontario, Canada.
Department of Biochemistry, University of Toronto, Toronto, Ontario, Canada.
J Immunol. 2024 Oct 1;213(7):988-997. doi: 10.4049/jimmunol.2400031.
Immune cells survey their microenvironment by forming dynamic cellular protrusions that enable chemotaxis, contacts with other cells, and phagocytosis. Podosomes are a unique type of protrusion structured by an adhesive ring of active integrins that surround an F-actin-rich core harboring degradative proteases. Although the features of podosomes, once-established, have been well defined, the steps that lead to podosome formation remain poorly understood by comparison. In this study, we report that spleen tyrosine kinase (Syk) is a critical regulator of podosome formation. Deletion of Syk or targeting its kinase activity eliminated the ability for murine macrophages to form podosomes. We found that the kinase activity of Syk was important for the phosphorylation of its substrates, HS1 and Pyk2, both of which regulate podosome formation. Additionally, before podosomes form, we report that the tandem Src homology 2 domains of Syk afforded multivalent clustering of ITAM-containing adaptors that associated with integrins to structure platforms that initiate podosomes. We therefore propose that Syk has a dual role in regulating podosomes: first, by facilitating the assembly of multivalent signaling hubs that nucleate their formation and second, by sustaining tyrosine kinase activity of the podosomes once they form against their substrates. In cells expressing recently identified gain-of-function variants of SYK, podosomes were dysregulated. These results implicate SYK in the (patho)physiological functions of podosomes in macrophages.
免疫细胞通过形成动态细胞突起监测其微环境,这些突起能够实现趋化作用、与其他细胞接触以及吞噬作用。足体是一种独特的突起类型,由活性整合素的粘附环构成,该粘附环围绕着富含F-肌动蛋白且含有降解蛋白酶的核心。尽管足体一旦形成后的特征已得到充分定义,但相比之下,导致足体形成的步骤仍知之甚少。在本研究中,我们报告脾酪氨酸激酶(Syk)是足体形成的关键调节因子。删除Syk或靶向其激酶活性消除了小鼠巨噬细胞形成足体的能力。我们发现Syk的激酶活性对其底物HS1和Pyk2的磷酸化很重要,这两者都调节足体形成。此外,在足体形成之前,我们报告Syk的串联Src同源2结构域提供了含免疫受体酪氨酸激活基序(ITAM)的衔接蛋白的多价聚集,这些衔接蛋白与整合素相关联以构建启动足体的平台。因此,我们提出Syk在调节足体方面具有双重作用:首先,通过促进多价信号枢纽的组装来启动足体的形成;其次,在足体形成后维持其针对底物的酪氨酸激酶活性。在表达最近鉴定出的SYK功能获得性变体的细胞中,足体失调。这些结果表明SYK参与巨噬细胞中足体的(病理)生理功能。