Hunzicker-Dunn M, Jungmann R A
Endocrinology. 1978 Aug;103(2):431-40. doi: 10.1210/endo-103-2-431.
DEAE-cellulose chromatography of the 105,000 X g supernatant fraction (cytosol) obtained from popped estrous rabbit follicles revealed the presence of a single form of cAMP-dependent protein kinase, designated protein kinase 3. The iv injection of an ovulatory dose of hCG to estrous rabbits promoted the appearance of a second, transient peak of cytosol cAMP-dependent protein kinase, protein kinase 1. Protein kinase 1 was detected within 10 min of hCG administration but had regressed to undetectable levels by 24 h in corpora lutea (CL) of pseudopregnancy and by 72 h in CL of pregnancy. Ovulation and subsequent CL formation were accompanied by the appearance of a third form of cAMP-dependent protein kinase, designated protein kinase 2. Protein kinase 2 was present within 2 h after hCG administration and persisted as a major form of cytosol cAMP-dependent protein kinase throughout the life span of CL. All three forms of protein kinase were inhibited by the heat-stable protein kinase inhibitor from rabbit skeletal muscle, possessed cAMP-binding activity, and were markedly stimulated by 10(-7) M cAMP. The activity of protein kinase 3 in CL of pregnancy, in corpora albicantia, and in interstitial tissue was markedly greater than that in follicles or in CL of pseudopregnancy, while the activity of protein kinase 2 remained relatively constant throughout the luteal life span. The iv injection of a luteolytic dose of hCG to 4-day pseudopregnant rabbits promoted no alterations of the protein kinase elution profile upon DEAE-cellulose chromatography of the luteal cytosol obtained 10 min to 3 days post-hCG injection. However, with dedifferentiation of corpora albicantia into interstitial tissue, the cAMP dependency of protein kinase 2 was reduced. The results indicate that the enzymatic activity and multiplicity of cAMP-dependent protein kinases in the cytosol of ovarian structures are subject to regulation by LH (hCG) and depend upon the various reproductive stages of the rabbit.
对从处于发情期的已排卵兔卵泡中获得的105,000×g上清液组分(胞质溶胶)进行二乙氨基乙基纤维素色谱分析,结果显示存在一种单一形式的环磷酸腺苷(cAMP)依赖性蛋白激酶,命名为蛋白激酶3。向处于发情期的兔子静脉注射排卵剂量的人绒毛膜促性腺激素(hCG),促使胞质溶胶中出现第二种短暂的cAMP依赖性蛋白激酶峰,即蛋白激酶1。在给予hCG后10分钟内检测到蛋白激酶1,但在假孕黄体(CL)中到24小时时其水平已降至检测不到,在妊娠黄体中到72小时时也是如此。排卵及随后的黄体形成伴随着第三种形式的cAMP依赖性蛋白激酶的出现,命名为蛋白激酶2。蛋白激酶2在给予hCG后2小时内出现,并在黄体的整个生命周期中作为胞质溶胶cAMP依赖性蛋白激酶的主要形式持续存在。所有三种形式的蛋白激酶均被来自兔骨骼肌的热稳定蛋白激酶抑制剂所抑制,具有cAMP结合活性,并被10⁻⁷M的cAMP显著刺激。妊娠黄体、白体和间质组织中蛋白激酶3的活性明显高于卵泡或假孕黄体中的活性,而蛋白激酶2的活性在黄体的整个生命周期中保持相对恒定。向4天假孕兔子静脉注射溶黄体剂量的hCG,在注射hCG后10分钟至3天获得的黄体胞质溶胶进行二乙氨基乙基纤维素色谱分析时,未促进蛋白激酶洗脱图谱的改变。然而,随着白体向间质组织去分化,蛋白激酶2对cAMP的依赖性降低。结果表明,卵巢结构胞质溶胶中环磷酸腺苷依赖性蛋白激酶的酶活性和多样性受促黄体生成素(hCG)调控,并取决于兔子的不同生殖阶段。