Nakagawa Y, Oxford G E, Ishibashi K, Yamamoto H, Maeda N, Bowen E, Brayer J, Humphreys-Beher M G
Department of Oral and Maxillofacial Surgery, Tsurumi University Dental School, Yokohama, Japan.
Biochem Pharmacol. 1997 Jan 24;53(2):233-40. doi: 10.1016/s0006-2952(96)00733-2.
Based on previous observations of the presence of both insulin-like growth factors I and II (IGF-I and IGF-II) in murine saliva (kerr et al., Biochem Pharmacol 49: 1521-1531, 1995), the saliva from BALB/c and Non-obese diabetic (NOD) mice was examined for the presence of insulin-like growth factor binding proteins (IGFBPs). Using a western-blot type ligand binding assay with 125I-labeled IGF-I, a series of binding proteins with molecular masses (M), between 25 and 45 kDa were detected in the sera, but not saliva, from both BALB/c and diabetic NOD mice. In the diabetic NOD mice, there were detectable changes in the concentrations of several of the IGFBPs relative to BALB/c mice. Using specific antibody to the binding proteins, one of these was identified as IGFBP-2. Gavage administration of [125I]IGFI indicated substantial uptake from the gastrointestinal tract and significant tissue distribution. There was an increase in serum concentrations of radiolabeled IGF-I in diabetic NOD mice over that in BALB/c mice but less recovered from most of the tissues. Intact 125I-labeled IGF-I was extracted and purified from various tissues, following gavage, and shown to retain biological activity. Thus, the uptake of biologically active IGFs from saliva would appear to take place independently of specific binding proteins.
基于之前在小鼠唾液中发现胰岛素样生长因子I和II(IGF-I和IGF-II)的观察结果(Kerr等人,《生物化学与药理学》49: 1521 - 1531,1995),对BALB/c和非肥胖糖尿病(NOD)小鼠的唾液进行了胰岛素样生长因子结合蛋白(IGFBPs)检测。使用125I标记的IGF-I进行蛋白质印迹类型的配体结合测定,在BALB/c和糖尿病NOD小鼠的血清中检测到一系列分子量(M)在25至45 kDa之间的结合蛋白,但在唾液中未检测到。在糖尿病NOD小鼠中,相对于BALB/c小鼠,几种IGFBPs的浓度存在可检测到的变化。使用针对结合蛋白的特异性抗体,其中一种被鉴定为IGFBP-2。经口灌胃给予[125I]IGF-I表明其从胃肠道有大量摄取和显著的组织分布。糖尿病NOD小鼠血清中放射性标记的IGF-I浓度高于BALB/c小鼠,但从大多数组织中回收的较少。经口灌胃后,从各种组织中提取并纯化了完整的125I标记的IGF-I,并显示其保留了生物活性。因此,从唾液中摄取生物活性IGF似乎独立于特异性结合蛋白发生。