Bandurska Katarzyna, Król Izabela, Myga-Nowak Magdalena
Zakład Mikrobiologii i Biotechnologii, Instytut Chemii, Ochrony Środowiska i Biotechnologii, Akademia im. Jana Długosza w Częstochowie.
Postepy Hig Med Dosw (Online). 2014 May 6;68:428-40. doi: 10.5604/17322693.1101229.
Interferons are a family of proteins that are released by a variety of cells in response to infections caused by viruses. Currently, we distinguish three types of interferons. They are classified based on the nucleotide sequence, interaction with specific receptors, chromosomal location, structure and physicochemical properties. The following interferons are classified as type I: α, β, ω, κ, ε, ζ, τ, δ, ν. They are recognized and bound by a receptor formed by two peptides, IFN-αR1 and IFN-αR2. Representative of type II interferons is interferon-γ. It binds to a receptor composed of chains IFNGR-1 and IFNGR-2. The recently classified type III interferons comprise IFN-λ1, IFN-λ2, and IFN-λ3. They act on receptors formed by λR1 IFN-and IL-10R2 subunits. A high level of antiviral protection is achieved by IFN-α, IFN-β and IFN-λ. Antiviral activity of interferons is based on the induction and regulation of innate and acquired immune mechanisms. By binding to transmembrane receptors, IFN interacts with target cells mainly by activating the JAK/STAT, but also other signaling pathways. This leads to induction and activation of many antiviral agents, such as protein kinase RNA-activated (PKR), ribonuclease 2-5A pathway, and Mx proteins, as well as numerous apoptotic pathways. As a result of the protective effect of interferons, the virus binding to cells and viral particles penetration into cells is stopped, and the release of the nucleocapsid from an envelope is suppressed. Disruption of transcription and translation processes of the structural proteins prevents the formation of virions or budding of viruses, and as a result degradation of the viral mRNA; the started processes inhibit the chain synthesis of viral proteins and therefore further stimulate the immune system cells.
干扰素是一类蛋白质,由多种细胞在受到病毒感染时释放。目前,我们区分出三种类型的干扰素。它们根据核苷酸序列、与特定受体的相互作用、染色体定位、结构和物理化学性质进行分类。以下干扰素被归类为I型:α、β、ω、κ、ε、ζ、τ、δ、ν。它们由两种肽IFN-αR1和IFN-αR2形成的受体识别并结合。II型干扰素的代表是干扰素-γ。它与由IFNGR-1和IFNGR-2链组成的受体结合。最近分类的III型干扰素包括IFN-λ1、IFN-λ2和IFN-λ3。它们作用于由λR1 IFN和IL-10R2亚基形成的受体。IFN-α、IFN-β和IFN-λ可实现高水平的抗病毒保护。干扰素的抗病毒活性基于先天和后天免疫机制的诱导和调节。通过与跨膜受体结合,IFN主要通过激活JAK/STAT以及其他信号通路与靶细胞相互作用。这导致许多抗病毒因子的诱导和激活,如蛋白激酶RNA激活(PKR)、核糖核酸酶2-5A途径和Mx蛋白,以及众多凋亡途径。由于干扰素的保护作用,病毒与细胞的结合以及病毒颗粒进入细胞的过程被阻止,核衣壳从包膜中的释放也受到抑制。结构蛋白转录和翻译过程的中断阻止了病毒粒子的形成或病毒出芽,结果导致病毒mRNA降解;启动的过程抑制病毒蛋白的链合成,因此进一步刺激免疫系统细胞。