Su C L, Austic R E
Department of Animal Science, Cornell University, Ithaca, New York 14853, USA.
Poult Sci. 1998 Dec;77(12):1852-7. doi: 10.1093/ps/77.12.1852.
L-Arginine is the precursor of NO, a cytotoxic agent of macrophages. Studies were carried out to determine whether dipeptides containing arginine can be utilized by lipopolysaccharide (LPS)-activated avian macrophages for NO production. A chicken macrophage cell line, the HD11 cell, was used in all experiments. Peptidase activities were observed in fetal bovine serum (FBS) and macrophage serum free medium (Mac-SFM). Therefore, the utilization of dipeptides by macrophages was examined using Dulbecco's modified Eagle medium (D-MEM), a chemically defined medium, in short-term culture without FBS. Nitrite accumulation in the culture medium was used as the indicator of NO production. At concentrations of 0.15 mM in the culture media, L-leucinyl-L-arginine was 89% as effective as L-arginine in providing substrate for NO production. L-Argininyl-L-leucine was 38% as effective as L-arginine. The effectiveness increased to 93 and 58%, respectively, when the concentrations of dipeptides and arginine were 1.0 mM. Both values were slightly higher in a second experiment (97 and 70%, respectively). L-Lysine (10 mM) inhibited nitrite formation from all three sources of L-arginine. In studies of initial rates of transport by HD11 cells in Hanks Balanced Salts solution (HBSS), both L-argininyl-L-leucine and L-leucinyl-L-arginine inhibited arginine uptake. As lysine and arginine share a common transporter for cationic amino acids and are known to compete for transport, these studies suggest that the peptides were hydrolyzed extracellularly, yielding arginine that was transported into the cell where it served as a substrate for NO synthesis.
L-精氨酸是一氧化氮(NO)的前体,而NO是巨噬细胞的一种细胞毒性因子。开展了多项研究以确定含精氨酸的二肽是否能被脂多糖(LPS)激活的禽类巨噬细胞用于产生NO。所有实验均使用鸡巨噬细胞系HD11细胞。在胎牛血清(FBS)和巨噬细胞无血清培养基(Mac-SFM)中观察到了肽酶活性。因此,在无FBS的短期培养中,使用化学成分明确的培养基——杜氏改良伊格尔培养基(D-MEM)来检测巨噬细胞对二肽的利用情况。培养基中亚硝酸盐的积累用作NO产生的指标。在培养基浓度为0.15 mM时,L-亮氨酰-L-精氨酸在为NO产生提供底物方面的有效性是L-精氨酸的89%。L-精氨酰-L-亮氨酸的有效性是L-精氨酸的38%。当二肽和精氨酸的浓度为1.0 mM时,有效性分别提高到93%和58%。在第二个实验中,这两个值略高(分别为97%和70%)。L-赖氨酸(10 mM)抑制了来自所有三种L-精氨酸来源的亚硝酸盐形成。在HD11细胞于汉克斯平衡盐溶液(HBSS)中转运初始速率的研究中,L-精氨酰-L-亮氨酸和L-亮氨酰-L-精氨酸均抑制精氨酸摄取。由于赖氨酸和精氨酸共享阳离子氨基酸的共同转运体,并且已知它们会竞争转运,这些研究表明这些肽在细胞外被水解,产生精氨酸,然后被转运到细胞内,在那里它作为NO合成的底物。