A. N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia.
Physical Department, Lomonosov Moscow State University, 119991 Moscow, Russia.
Cells. 2021 Mar 5;10(3):563. doi: 10.3390/cells10030563.
During infection or certain metabolic disorders, neutrophils can escape from blood vessels, invade and attach to other tissues. The invasion and adhesion of neutrophils is accompanied and maintained by their own secretion. We have previously found that adhesion of neutrophils to fibronectin dramatically and selectively stimulates the release of the free amino acid hydroxylysine. The role of hydroxylysine and lysyl hydroxylase in neutrophil adhesion has not been studied, nor have the processes that control them. Using amino acid analysis, mass spectrometry and electron microscopy, we found that the lysyl hydroxylase inhibitor minoxidil, the matrix metalloproteinase inhibitor doxycycline, the PI3K/Akt pathway inhibitors wortmannin and the Akt1/2 inhibitor and drugs that affect the actin cytoskeleton significantly and selectively block the release of hydroxylysine and partially or completely suppress spreading of neutrophils. The actin cytoskeleton effectors and the Akt 1/2 inhibitor also increase the phenylalanine release. We hypothesize that hydroxylysine release upon adhesion is the result of the activation of lysyl hydroxylase in interaction with matrix metalloproteinase, the PI3K/Akt pathway and intact actin cytoskeleton, which play important roles in the recruitment of neutrophils into tissue through extracellular matrix remodeling.
在感染或某些代谢紊乱期间,中性粒细胞可以从血管中逸出,侵入并附着到其他组织上。中性粒细胞的侵入和黏附伴随着并由其自身的分泌维持。我们之前发现,中性粒细胞对纤维连接蛋白的黏附显著且选择性地刺激了游离氨基酸羟赖氨酸的释放。羟赖氨酸和赖氨酰羟化酶在中性粒细胞黏附中的作用尚未得到研究,也没有研究控制它们的过程。使用氨基酸分析、质谱和电子显微镜,我们发现赖氨酰羟化酶抑制剂米诺地尔、基质金属蛋白酶抑制剂强力霉素、PI3K/Akt 通路抑制剂渥曼青霉素和 Akt1/2 抑制剂以及影响肌动蛋白细胞骨架的药物可显著且选择性地阻断羟赖氨酸的释放,并部分或完全抑制中性粒细胞的扩展。肌动蛋白细胞骨架效应物和 Akt1/2 抑制剂也增加了苯丙氨酸的释放。我们假设,黏附后羟赖氨酸的释放是赖氨酰羟化酶在与基质金属蛋白酶、PI3K/Akt 通路和完整的肌动蛋白细胞骨架相互作用下被激活的结果,这些通路在通过细胞外基质重塑将中性粒细胞募集到组织中发挥着重要作用。