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肺泡巨噬细胞上胰岛素样生长因子(IGF)受体的表达:IGF诱导的肌醇磷酸(InsPi)形成、细胞内钙离子浓度([Ca2+]i)和细胞内pH值(pHi)的变化。

Expression of IGF receptors on alveolar macrophages: IGF-induced changes in InsPi formation, [Ca2+]i, and pHi.

作者信息

Geertz R, Kiess W, Kessler U, Hoeflich A, Tarnok A, Gercken G

机构信息

University of Hamburg, Institute of Biochemistry and Food Chemistry, Department of Biochemistry and Molecular Biology, Germany.

出版信息

Mol Cell Biochem. 1997 Dec;177(1-2):33-45. doi: 10.1023/a:1006836631673.

Abstract

Expression of insulin-like growth factor-I (IGF-I) receptors and insulin-like growth factor-II/mannose-6-phosphate (IGF-II/Man6P) receptors in cultured bovine alveolar macrophages (BAM) was demonstrated by competitive binding studies and crosslinking experiments. Western blotting of protein extracts from cultured BAM using an anti bovine IGF-II/Man6P receptor antiserum (#66416) confirmed the presence of IGF-II/Man6P receptors on BAM. The effects of IGFs and Man6P on generation of inositol phosphates was measured by HPLC analysis of perchloric acid extracts from myo-[3H]inositol-labelled cultured BAM. IGF-I at nanomolar concentrations and Man6P (10[-8]-10[-3] M) stimulated the accumulation of both Ins(1,4,5)P3 and Ins(1,3,4,5)P4 after 30 sec. IGF-II (up to 2.3 x 10[-8] M) had no significant effect on inositol phosphate accumulation under the same conditions. Both IGFs and Man6P induced a rise in [Ca2+]i in cultured BAM. In addition, using the fluorescent dye SNARF-1/AM we could demonstrate rapid but small IGF-II (10[-9] M) triggered acidification (0.07 pH units) of cultured BAM. Taken together, our results indicate not only the presence of both IGF-I and IGF-II/Man6P receptors on BAM, but also provide evidence of the linkage of the IGF-I receptor to the inositol phosphate system.

摘要

通过竞争性结合研究和交联实验证明了胰岛素样生长因子-I(IGF-I)受体和胰岛素样生长因子-II/甘露糖-6-磷酸(IGF-II/Man6P)受体在培养的牛肺泡巨噬细胞(BAM)中的表达。使用抗牛IGF-II/Man6P受体抗血清(#66416)对培养的BAM的蛋白质提取物进行蛋白质印迹分析,证实了BAM上存在IGF-II/Man6P受体。通过对来自肌醇-[3H]肌醇标记的培养BAM的高氯酸提取物进行HPLC分析,测量了IGF和Man6P对肌醇磷酸生成的影响。纳摩尔浓度的IGF-I和Man6P(10[-8]-10[-3]M)在30秒后刺激了Ins(1,4,5)P3和Ins(1,3,4,5)P4的积累。在相同条件下,IGF-II(高达2.3 x 10[-8]M)对肌醇磷酸积累没有显著影响。IGF和Man6P均诱导培养的BAM中[Ca2+]i升高。此外,使用荧光染料SNARF-1/AM,我们可以证明IGF-II(10[-9]M)触发培养的BAM快速但微小的酸化(0.07个pH单位)。综上所述,我们的结果不仅表明BAM上存在IGF-I和IGF-II/Man6P受体,还提供了IGF-I受体与肌醇磷酸系统相关联的证据。

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