Department of Anthropology, Washington University, St. Louis, MO, United States.
Departments of Structural Biology and Microbiology & Immunology, Stanford University School of Medicine, Stanford, CA, United States.
Front Immunol. 2019 Feb 19;10:177. doi: 10.3389/fimmu.2019.00177. eCollection 2019.
Natural killer (NK) cells have diverse roles in hominid immunity and reproduction. Modulating these functions are the interactions between major histocompatibility complex (MHC) class I molecules that are ligands for two NK cell surface receptor types. Diverse killer cell immunoglobulin-like receptors (KIR) bind specific motifs encoded within the polymorphic MHC class I cell surface glycoproteins, while, in more conserved interactions, CD94:NKG2A receptors recognize MHC-E with bound peptides derived from MHC class I leader sequences. The hominid lineage presents a choreographed co-evolution of KIR with their MHC class I ligands. , and are present in all great apes with species-specific haplotypic variation in gene content. The Bw4 epitope recognized by lineage II KIR is restricted to MHC-B but also present on some gorilla and human MHC-A. Common to great apes, but rare in humans, are MHC-B possessing a C1 epitope recognized by lineage III KIR. arose from duplication of and is fixed in all great apes except orangutan, where it exists on approximately 50% of haplotypes and all allotypes are C1-bearing. Recent study showed that gorillas possess yet another intermediate organization compared to humans. Like orangutans, but unlike the species, duplication of occurred. However, is fixed, and the MHC-C C2 epitope (absent in orangutans) emerges. The evolution of MHC-C drove expansion of its cognate lineage III KIR. Recently, position -21 of the MHC-B leader sequence has been shown to be critical in determining NK cell educational outcome. In humans, methionine (-21M) results in CD94:NKG2A-focused education whereas threonine (-21T) produces KIR-focused education. This is another dynamic position among hominids. Orangutans have exclusively -21M, consistent with their intermediate stage in lineage III KIR-focused evolution. Gorillas have both -21M and -21T, like humans, but they are unequally encoded by their duplicated genes. Chimpanzees have near-fixed -21T, indicative of KIR-focused NK education. Harmonious with this observation, chimpanzee KIR exhibit strong binding and, compared to humans, smaller differences between binding levels of activating and inhibitory KIR. Consistent between these MHC-NK cell receptor systems over the course of hominid evolution is the evolution of polymorphism favoring the more novel and dynamic KIR system.
自然杀伤 (NK) 细胞在人类免疫和生殖中具有多种作用。调节这些功能的是主要组织相容性复合体 (MHC) Ⅰ类分子与两种 NK 细胞表面受体类型之间的相互作用。不同的杀伤细胞免疫球蛋白样受体 (KIR) 结合 MHC Ⅰ类细胞表面糖蛋白中编码的特定基序,而在更保守的相互作用中,CD94:NKG2A 受体识别与 MHC Ⅰ类前导序列衍生肽结合的 MHC-E。人类谱系呈现出 KIR 与其 MHC Ⅰ类配体的协同进化。在所有的大型猿类中都存在 KIR3DL1 和 KIR2DL1,其基因内容在种系特异性单倍型变异中存在。谱系 II KIR 识别的 Bw4 表位仅限于 MHC-B,但也存在于一些大猩猩和人类 MHC-A 上。与大型猿类共有但在人类中罕见的是 MHC-B 具有谱系 III KIR 识别的 C1 表位。KIR3DL1 是由 KIR3DL1 的复制产生的,除了猩猩外,在所有的大型猿类中都是固定的,而在猩猩中,大约有 50%的单倍型存在,并且所有的同种异型都带有 C1。最近的研究表明,大猩猩与人类相比,具有另一种中间的 KIR3DL1 组织。与猩猩一样,但与 KIR3DL1 物种不同,KIR3DL1 发生了复制。然而,KIR3DL1 是固定的,并且 MHC-C C2 表位(在猩猩中不存在)出现。MHC-C 的进化推动了其同源性 III KIR 的扩张。最近,MHC-B 前导序列的位置 -21 被证明在决定 NK 细胞教育结果方面至关重要。在人类中,蛋氨酸 (-21M) 导致 CD94:NKG2A 为焦点的教育,而苏氨酸 (-21T) 产生 KIR 为焦点的教育。这是人类中的另一个动态位置。猩猩仅具有 -21M,与它们处于 KIR3DL1 为焦点的进化的中间阶段一致。大猩猩既有 -21M 又有 -21T,与人类一样,但它们由其复制的 KIR3DL1 基因不均等地编码。黑猩猩几乎固定的 -21T 表明 KIR 为焦点的 NK 教育。与这一观察结果一致的是,黑猩猩 KIR 表现出强烈的结合,与人类相比,激活和抑制性 KIR 的结合水平差异较小。在人类进化过程中,这些 MHC-NK 细胞受体系统之间的一致性是有利于更新型和动态的 KIR 系统的多态性进化。