小鼠淋巴样细胞系的肾上腺素能受体和腺苷酸环化酶活性。

M Staehelin, P Müller, M Portenier, A W Harris
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摘要

通过与亲水性配体[3H]CGP-12177结合,在16种培养的T淋巴和b淋巴衍生肿瘤细胞系中检测β -肾上腺素能受体。每个细胞的受体数量从不到100个到超过3000个不等。细胞内cAMP对异丙肾上腺素和福斯克林的反应在7个具有一定受体数量的细胞系中被测量。异丙肾上腺素诱导的cAMP升高与受体数量之间没有直接关系,而福斯克林诱导的cAMP升高在不同细胞系之间的差异超过100倍。腺苷酸环化酶活性也在7个细胞系的膜制剂中进行了测定。t -淋巴瘤细胞系WEHI-22是受体数量最多的细胞系(每个细胞3700个),对任何刺激剂的反应都很小。对于其他四种具有受体的细胞系,发现异丙肾上腺素引起的膜结合腺苷酸环化酶活性相对于福斯克林引起的活性与每个细胞的受体数量成正比。因此,受体的数量似乎决定了内在腺苷酸环化酶的比例,这种酶可以被β -肾上腺素能剂激活。与福斯克林诱导的相比,GppNHp和氟化物诱导的膜内腺苷酸环化酶水平在某些细胞系中明显高于其他细胞系。这些数据和WEHI-22细胞的结果表明,淋巴样细胞系在功能C和N蛋白的含量上存在差异。
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beta-Adrenergic receptors and adenylate cyclase activity in murine lymphoid cell lines.

beta-Adrenergic receptors were determined in sixteen cultured tumor cell lines of T- and B-lymphoid derivation by the binding of the hydrophilic ligand [3H]CGP-12177. The number of receptors per cell varied from less than a hundred to over three thousand. Intracellular cAMP responses to isoproterenol and forskolin were measured for seven cell lines possessing a range of receptor numbers. No direct relationship was found between the isoproterenol-induced elevation of cAMP and the receptor number, and forskolin-induced increases in cAMP varied by more than 100-fold between cell lines. Adenylate cyclase activity was also measured in membrane preparations from the seven cell lines. The T-lymphoma line WEHI-22, the line with the highest receptor number (3700 per cell), showed very little response to any stimulatory agent. With the other four cell lines possessing receptors, the membrane-bound adenylate cyclase activity evoked by isoproterenol relative to that evoked by forskolin was found to be proportional to the number of receptors per cell. The number of receptors thus seems to determine the proportion of the inherent adenylate cyclase that can be activated by a beta-adrenergic agent. The levels of adenylate cyclase induced in membranes by GppNHp and by fluoride, relative to those induced by forskolin, were substantially higher with some cell lines than with others. These data and the results from WEHI-22 cells indicate that lymphoid cell lines differ in their content of functional C and N proteins.

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