Bazzoni F, Cassatella M A, Rossi F, Ceska M, Dewald B, Baggiolini M
Institute of General Pathology, University of Verona, Italy.
J Exp Med. 1991 Mar 1;173(3):771-4. doi: 10.1084/jem.173.3.771.
After phagocytosis of yeast opsonized with IgG, neutrophil leukocytes (polymorphonuclear leukocytes [PMN]) expressed high levels of neutrophil-activating peptide 1/interleukin 8 (NAP-1/IL-8) mRNA, which peaked after 3-5 h and were still elevated after 18 h. A similar but quantitatively less prominent effect was obtained with lipopolysaccharide (LPS). After phagocytosis, but not after exposure to LPS, the PMN progressively released considerable amounts of NAP-1/IL-8 into the culture medium (18.6-50 ng/ml in 18 h). The peptide released was biologically active, as indicated by the transient elevation of cytosolic-free calcium in PMN exposed to aliquots of the culture supernatants, and desensitization by prestimulation of the cells with recombinant NAP-1/IL-8. By producing NAP-1/IL-8 at sites where they phagocytose invading microorganisms, PMN could enhance the recruitment of new defense cells.
在用IgG调理过的酵母被吞噬后,中性粒细胞(多形核白细胞[PMN])表达高水平的中性粒细胞激活肽1/白细胞介素8(NAP-1/IL-8)mRNA,其在3-5小时后达到峰值,并在18小时后仍保持升高。脂多糖(LPS)也有类似但在数量上不太显著的作用。吞噬后,而不是暴露于LPS后,PMN逐渐向培养基中释放大量的NAP-1/IL-8(18小时内为18.6-50 ng/ml)。释放的肽具有生物活性,这通过暴露于培养上清液等分试样的PMN中游离钙离子的短暂升高以及用重组NAP-1/IL-8对细胞进行预刺激后的脱敏来表明。通过在吞噬入侵微生物的部位产生NAP-1/IL-8,PMN可以增强新防御细胞的募集。