Reichner J S, Meszaros A J, Louis C A, Henry W L, Mastrofrancesco B, Martin B A, Albina J E
Department of Surgery, Division of Surgical Research, Brown University and Rhode Island Hospital, Providence, Rhode Island 02903, USA.
Am J Pathol. 1999 Apr;154(4):1097-104. doi: 10.1016/S0002-9440(10)65362-X.
Tissue injury initiates a temporally ordered sequence of local cellular and metabolic responses presumably necessary for successful repair. Previous investigations demonstrated that metabolic evidence for nitric oxide synthase (NOS) activity is detectable in wounds only during the initial 48 to 72 hours of the repair process. Present results identify the cell types contributing inducible NOS (iNOS) to experimental wounds in rats. iNOS antigen was expressed in most macrophages present in wounds 6 to 24 hours after injury, and these cells exhibited NAPDH diaphorase and NOS activity. Polymorphonuclear leukocytes contained little iNOS antigen and no NADPH diaphorase activity and were minimally able to convert L-arginine to L-citrulline. The frequency of iNOS-positive macrophages declined on days 3 and 5 after wounding. By day 10, most macrophages in the wound were negative for iNOS. These cells, however, acquired iNOS antigen and activity in culture. Wound fluids, but not normal rat serum, suppressed the induction of iNOS during culture. Findings indicate that the expression of iNOS in healing wounds is restricted to macrophages present during the early phases of repair and that components of wound fluid suppress the induction of iNOS in macrophages in late wounds. Polymorphonuclear leukocytes contribute little iNOS activity to the healing wound.
组织损伤引发了一系列按时间顺序排列的局部细胞和代谢反应,这些反应可能是成功修复所必需的。先前的研究表明,一氧化氮合酶(NOS)活性的代谢证据仅在修复过程的最初48至72小时内在伤口中可检测到。目前的结果确定了在大鼠实验性伤口中产生诱导型NOS(iNOS)的细胞类型。iNOS抗原在损伤后6至24小时伤口中的大多数巨噬细胞中表达,并且这些细胞表现出NAPDH黄递酶和NOS活性。多形核白细胞几乎不含iNOS抗原,也没有NADPH黄递酶活性,并且将L-精氨酸转化为L-瓜氨酸的能力最低。伤口后第3天和第5天,iNOS阳性巨噬细胞的频率下降。到第10天,伤口中的大多数巨噬细胞iNOS呈阴性。然而,这些细胞在培养中获得了iNOS抗原和活性。伤口液而非正常大鼠血清在培养期间抑制了iNOS的诱导。研究结果表明,愈合伤口中iNOS的表达仅限于修复早期存在的巨噬细胞,并且伤口液成分抑制晚期伤口巨噬细胞中iNOS的诱导。多形核白细胞对愈合伤口的iNOS活性贡献很小。