Department of Microbiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Applied Bioinformatics Center, St Jude Children's Research Hospital, Memphis, TN, USA.
EMBO Mol Med. 2022 Jan 11;14(1):e14485. doi: 10.15252/emmm.202114485. Epub 2021 Nov 26.
SPINK6 was identified in human skin as a cellular inhibitor of serine proteases of the KLK family. Airway serine proteases are required to cleave hemagglutinin (HA) of influenza A viruses (IAVs) to initiate an infection in the human airway. We hypothesized that SPINK6 may inhibit common airway serine proteases and restrict IAV activation. We demonstrate that SPINK6 specifically suppresses the proteolytic activity of HAT and KLK5, HAT- and KLK5-mediated HA cleavage, and restricts virus maturation and replication. SPINK6 constrains the activation of progeny virions and impairs viral growth; and vice versa, blocking endogenous SPINK6 enhances HA cleavage and viral growth in physiological-relevant human airway organoids where SPINK6 is intrinsically expressed. In IAV-infected mice, SPINK6 significantly suppresses viral growth and improves mouse survival. Notably, individuals carrying the higher SPINK6 expression allele were protected from human H7N9 infection. Collectively, SPINK6 is a novel host inhibitor of serine proteases in the human airway and restricts IAV activation.
SPINK6 最初在人类皮肤中被鉴定为 KLK 家族丝氨酸蛋白酶的细胞抑制剂。气道丝氨酸蛋白酶需要切割甲型流感病毒 (IAV) 的血凝素 (HA) 才能在人体气道中引发感染。我们假设 SPINK6 可能会抑制常见的气道丝氨酸蛋白酶并限制 IAV 的激活。我们证明 SPINK6 可特异性抑制 HAT 和 KLK5 的蛋白水解活性、HAT 和 KLK5 介导的 HA 切割,从而限制病毒成熟和复制。SPINK6 限制了子代病毒颗粒的激活,并损害了病毒生长;反之,阻断内源性 SPINK6 会增强生理相关的人呼吸道类器官中 HA 的切割和病毒生长,而 SPINK6 内在表达于其中。在感染 IAV 的小鼠中,SPINK6 显著抑制了病毒生长并提高了小鼠的存活率。值得注意的是,携带 SPINK6 高表达等位基因的个体可免受人感染 H7N9 的影响。总之,SPINK6 是人类气道中丝氨酸蛋白酶的一种新型宿主抑制剂,可限制 IAV 的激活。