Vieira-Coelho M A, Teixeira V L, Guimarães J T, Serrão M P, Soares-da-Silva P
Institute of Pharmacology & Therapeutics, Faculty of Medicine, Porto, Portugal.
Life Sci. 1999;64(1):69-81. doi: 10.1016/s0024-3205(98)00535-9.
To explore the usefulness of Caco-2 cells in the study of intestinal dopaminergic and 5-hydroxytryptaminergic physiology, we have undertaken the study of aromatic L-amino acid decarboxylase (AADC), catechol-O-methyltransferase (COMT) and type A and B monoamine oxidase (MAO-A and MAO-B) activities in these cells using specific substrates. The activity of these enzymes was also evaluated in isolated rat jejunal epithelial cells. The results showed that Vmax values (in nmol mg protein(-1) h(-1)) for AADC, using L-DOPA as the substrate, in rat jejunal epithelial cells (127.3+/-11.4) were found to be 6-fold higher than in Caco-2 cells (22.5+/-2.6). However, Km values in Caco-2 cells (1.24+/-0.37 mM) were similar to those observed in rat jejunal epithelial cells (1.30+/-0.29 mM). Similar results were obtained when AADC activity was evaluated using L-5HTP as substrate; in rat jejunal epithelial cells Vmax values (in nmol mg prot(-1) h(-1)) were found to be 5-fold that in Caco-2 cells (16.3+/-1.0 and 3.0+/-0.2, respectively), and Km values in Caco-2 cells (0.23+/-0.08 mM) were again similar to those observed in rat intestinal epithelial cells (0.09+/-0.03 mM). Caco-2 cells were not able to O-methylate dopamine, in contrast to rat jejunal epithelial cells (Vmax = 8.6+/-0.4 nmol mg protein(-1)(h-1); Km = 516+/-57 microM). Vmax values (in nmol mg protein(-1)(h-1)) for type A and B MAO in Caco-2 cells (19.0+/-0.6 and 5.4+/-0.6, respectively) were found to be significantly lower (P<0.05) than those in rat jejunal epithelial cells (46.9+/-3.1 and 9.6+/-1.2, respectively); however, no significant differences in the Km values were observed between Caco-2 and rat jejunal epithelial cells for both type A and B MAO. In conclusion, Caco-2 cells in culture are endowed with the synthetic and metabolic machinery needed to form and degrade DA and 5-HT, though, no COMT activity could be detected in these cells.
为了探究Caco-2细胞在肠道多巴胺能和5-羟色胺能生理学研究中的作用,我们使用特定底物对这些细胞中的芳香族L-氨基酸脱羧酶(AADC)、儿茶酚-O-甲基转移酶(COMT)以及A型和B型单胺氧化酶(MAO-A和MAO-B)的活性进行了研究。我们还对分离出的大鼠空肠上皮细胞中的这些酶的活性进行了评估。结果显示,以L-DOPA为底物时,大鼠空肠上皮细胞中AADC的Vmax值(以nmol mg蛋白⁻¹ h⁻¹计)为(127.3±11.4),比Caco-2细胞中的(22.5±2.6)高6倍。然而,Caco-2细胞中的Km值(1.24±0.37 mM)与大鼠空肠上皮细胞中观察到的(1.30±0.29 mM)相似。当以L-5HTP为底物评估AADC活性时,也得到了类似的结果;大鼠空肠上皮细胞中的Vmax值(以nmol mg蛋白⁻¹ h⁻¹计)是Caco-2细胞中的5倍(分别为16.3±1.0和3.0±0.2),且Caco-2细胞中的Km值(0.23±0.08 mM)再次与大鼠肠上皮细胞中观察到的(0.09±0.03 mM)相似。与大鼠空肠上皮细胞不同,Caco-2细胞不能使多巴胺发生O-甲基化(大鼠空肠上皮细胞:Vmax = 8.6±0.4 nmol mg蛋白⁻¹ h⁻¹;Km = 516±57 μM)。Caco-2细胞中A型和B型MAO的Vmax值(以nmol mg蛋白⁻¹ h⁻¹计)分别为(19.0±0.6和5.4±0.6),显著低于大鼠空肠上皮细胞中的(分别为46.9±3.1和9.6±1.2)(P<0.05);然而,对于A型和B型MAO,Caco-2细胞与大鼠空肠上皮细胞的Km值未观察到显著差异。总之,培养的Caco-2细胞具备合成和代谢DA与HT所需的机制,不过在这些细胞中未检测到COMT活性。