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兔气道平滑肌中肌醇1,4,5-三磷酸代谢的成熟调控

Maturational regulation of inositol 1,4,5-trisphosphate metabolism in rabbit airway smooth muscle.

作者信息

Rosenberg S M, Berry G T, Yandrasitz J R, Grunstein M M

机构信息

Division of Pulmonary Medicine, Joseph Stokes, Jr., Research Institute, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

J Clin Invest. 1991 Dec;88(6):2032-8. doi: 10.1172/JCI115531.

Abstract

Airway reactivity has been shown to vary with age; however, the mechanism(s) underlying this process remain unidentified. To elucidate the role of ontogenetic changes in phosphoinositide-linked signal transduction, we examined whether age-related differences in tracheal smooth muscle (TSM) contractility to carbachol (CCh) are associated with developmental changes in the production and metabolism of the second messenger, inositol 1,4,5-trisphosphate (Ins (1,4,5)P3). In TSM segments isolated from 2-wk-old and adult rabbits, both the maximal isometric contractile force and sensitivity (i.e., -logED50) to CCh (10(-10)-10(-4) M) were significantly greater in the immature vs. adult tissues (P less than 0.001). Similarly, Ins(1,4,5)P3 accumulation elicited by either receptor-coupled stimulation with CCh (10(-10)-10(-4) M) or post-receptor-mediated guanine nucleotide binding protein activation of permeabilized TSM with GTP gamma S (100 microM) was also significantly enhanced in 2-wk-old vs. adult TSM. Measurement of the activities of the degradative enzymes for Ins(1,4,5)P3 demonstrated that: (a) mean +/- SE maximal Ins(1,4,5)P3 3'-kinase activity was significantly reduced in the immature vs. adult TSM (i.e., approximately 71.7 +/- 6.0 vs. 137.8 +/- 10.0 pmol/min per mg protein, respectively; P less than 0.005); (b) by contrast, maximal Ins(1,4,5)P3 5'-phosphatase activity was significantly increased in the immature vs. adult TSM (i.e., 27.9 +/- 1.2 vs. 15.6 +/- 1.5 nmol/min per mg protein, respectively; P less than 0.001); and (c) the Km values for Ins(1,4,5)P3 5'-phosphatase were 14- and 19-fold greater than those for Ins(1,4,5)P3 3'-kinase in the 2-wk-old and adult TSM, respectively. Collectively, the findings suggest that the age-related decrease in agonist-induced rabbit TSM contractility is associated with a diminution in Ins(1,4,5)P3 accumulation which is attributed, at least in part, to ontogenetic changes in the relative activities of the degradative enzymes for Ins(1,4,5)P3.

摘要

气道反应性已被证明会随年龄而变化;然而,这一过程背后的机制仍不明晰。为阐明磷酸肌醇连接信号转导中个体发育变化的作用,我们研究了气管平滑肌(TSM)对卡巴胆碱(CCh)收缩性的年龄相关差异是否与第二信使肌醇1,4,5-三磷酸(Ins(1,4,5)P3)产生和代谢的发育变化相关。在从2周龄和成年兔子分离的TSM节段中,未成熟组织对CCh(10⁻¹⁰ - 10⁻⁴ M)的最大等长收缩力和敏感性(即-logED50)均显著高于成年组织(P < 0.001)。同样,用CCh(10⁻¹⁰ - 10⁻⁴ M)进行受体偶联刺激或用GTPγS(100 μM)对通透化的TSM进行受体后介导的鸟嘌呤核苷酸结合蛋白激活所引发的Ins(1,4,5)P3积累,在2周龄TSM中也显著高于成年TSM。对Ins(1,4,5)P3降解酶活性的测量表明:(a)未成熟TSM中Ins(1,4,5)P3 3'-激酶的平均±SE最大活性显著低于成年TSM(即分别约为71.7±6.0与137.8±10.0 pmol/min per mg蛋白;P < 0.005);(b)相比之下,未成熟TSM中Ins(1,4,5)P3 5'-磷酸酶的最大活性显著高于成年TSM(即分别为27.9±1.2与15.6±1.5 nmol/min per mg蛋白;P < 0.001);(c)在2周龄和成年TSM中,Ins(1,4,5)P3 5'-磷酸酶的Km值分别比Ins(1,4,5)P3 3'-激酶的Km值大14倍和19倍。总体而言,这些发现表明,激动剂诱导的兔TSM收缩性的年龄相关降低与Ins(1,4,5)P3积累的减少有关,这至少部分归因于Ins(1,4,5)P3降解酶相对活性的个体发育变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbeb/295795/a71d1a493909/jcinvest00065-0269-a.jpg

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