Haycock J W
LSUMC-BIOCHEM, New Orleans, LA 70119.
Neurochem Res. 1993 Jan;18(1):15-26. doi: 10.1007/BF00966919.
Intact bovine adrenal medullary chromaffin cells were preincubated with 32PO4, and the multiple-site phosphorylation of tyrosine hydroxylase (TH) was studied. Up to eight 32P-labeled peptides were produced by tryptic hydrolysis of TH; however, all of the tryptic phosphopeptides were derived from four phosphorylation sites--Ser8, Ser19, Ser31 and Ser40. In situ regulation of 32P incorporation into the latter three sites was demonstrated with a diverse set of pharmacological agents. 32P incorporation into Ser19 was preferentially increased by brief exposures to depolarizing secretagogues. Longer treatments also increased Ser31 and Ser40 phosphorylation. Nicotine, muscarine and vasoactive intestinal polypeptide--reflecting cholinergic and non-cholinergic components of sympatho-adrenal transmission--each produced different patterns of multiple-site phosphorylation of TH. Nicotine, bradykinin and histamine increased 32P incorporation at each of the three sites whereas muscarine, angiotensin II, endothelin III, prostaglandin E1, GABA and ATP selectively increased Ser31 phosphorylation. Nerve growth factor did not influence TH phosphorylation in chromaffin cells from adult adrenal glands but selectively increased Ser31 phosphorylation in chromaffin cells isolated from calf adrenal glands. 32P incorporation into Ser40 was selectively increased by forskolin and other cAMP-acting agents whereas vasoactive intestinal polypeptide increased Ser31 and Ser40 phosphorylation. Thus, the phosphorylation of TH in bovine chromaffin cells appears to be regulated at three sites by three separate intracellular signaling pathways--Ser19 via Ca2+/calmodulin-dependent protein kinase II; Ser31 via ERK (MAP2 kinases); and Ser40 via cAMP-dependent protein kinase. These signaling pathways, as well as the extracellular signals that were effective in stimulating them, are similar to those previously described for TH in rat pheochromocytoma cells. However, several of the pharmacological agents produced different patterns of multiple-site TH phosphorylation in the bovine chromaffin cells. These differences between tissues could be accounted for by differences in the coupling/access between the extracellular signal transduction systems and the intracellular signaling pathways as opposed to differences in the intracellular signaling pathways per se.
完整的牛肾上腺髓质嗜铬细胞用32PO4进行预孵育,然后研究酪氨酸羟化酶(TH)的多位点磷酸化。用胰蛋白酶水解TH可产生多达8种32P标记的肽段;然而,所有胰蛋白酶磷酸肽均来自4个磷酸化位点——Ser8、Ser19、Ser31和Ser40。用多种药理试剂证明了32P掺入后三个位点的原位调节。短暂暴露于去极化促分泌剂可优先增加32P掺入Ser19。较长时间的处理也会增加Ser31和Ser40的磷酸化。尼古丁、毒蕈碱和血管活性肠肽——反映交感-肾上腺传递的胆碱能和非胆碱能成分——各自产生不同的TH多位点磷酸化模式。尼古丁、缓激肽和组胺增加了三个位点中每个位点的32P掺入,而毒蕈碱、血管紧张素II、内皮素III、前列腺素E1、GABA和ATP选择性增加Ser31的磷酸化。神经生长因子对成年肾上腺嗜铬细胞中TH的磷酸化没有影响,但选择性增加了从小牛肾上腺分离的嗜铬细胞中Ser31的磷酸化。forskolin和其他cAMP作用剂选择性增加32P掺入Ser40,而血管活性肠肽增加Ser31和Ser40的磷酸化。因此,牛嗜铬细胞中TH的磷酸化似乎在三个位点由三种不同的细胞内信号通路调节——Ser19通过Ca2+/钙调蛋白依赖性蛋白激酶II;Ser31通过ERK(MAP2激酶);Ser40通过cAMP依赖性蛋白激酶。这些信号通路以及有效刺激它们的细胞外信号与先前在大鼠嗜铬细胞瘤细胞中描述的TH信号通路相似。然而,几种药理试剂在牛嗜铬细胞中产生了不同的TH多位点磷酸化模式。组织之间的这些差异可能是由细胞外信号转导系统与细胞内信号通路之间的偶联/通路差异造成的,而不是细胞内信号通路本身的差异。