Hirata M, Saito N, Kono M, Tanaka C
Department of Pharmacology, Kobe University School of Medicine, Japan.
Brain Res Dev Brain Res. 1991 Oct 21;62(2):229-38. doi: 10.1016/0165-3806(91)90170-n.
Differential expression of protein kinase C subspecies, beta I- and beta II-PKC, derived from a single gene by alternative splicing was evidenced in the postnatal developing rat brain. Immunoblot analysis of the PKC subspecies in the whole developing brain showed that beta I-PKC was present at birth and then gradually increased, while beta II-PKC was not present at birth or on postnatal day 3, then increased rapidly from day 7 to the maximum value seen in the adult brain. Under light microscopy, beta I-PKC immunoreactivities seen at birth were the most intense in the brainstem and intense in the diagonal bundle and globus pallidus. beta I-PKC immunoreactivities in these neurons weakened from day 7 and disappeared in the adult brain, while in the cerebral cortex, triangular septal nucleus and pontine nucleus beta I-PKC immunoreactivities were week at birth and then gradually increased. beta II-PKC immunoreactivities were first visible in neurons on day 7 and increased progressively. beta I- and beta II-PKCs were not co-localized in a neuron, as far as examined. The immunoreactivities of beta I-PKC at birth were localized in growth cone-like structures as well as in the dendrites and perikarya. Similarly, alpha-PKC was also present at birth in the growth cone-like structure. Immunoblot analysis revealed that beta I-PKC was present at birth in the growth cone-rich fraction from the hindbrain but not in that from the forebrain, while alpha-PKC was found in the growth cone-rich fraction from both the forebrain and the hindbrain. beta II- and gamma-PKC were not detected in the growth cone-rich fraction from either forebrain or hindbrain. These findings suggest that beta I- and beta II-PKC play a role in different stages of development and in different neurons; both beta-subspecies may be involved in postnatal developing neuronal functions while only beta I-PKC plays functional roles in the growth cone, in the prenatal developmental stage.
通过选择性剪接从单个基因衍生而来的蛋白激酶C亚型βI-PKC和βII-PKC在出生后发育的大鼠脑中存在差异表达。对整个发育中脑的PKC亚型进行免疫印迹分析表明,βI-PKC在出生时就存在,然后逐渐增加,而βII-PKC在出生时或出生后第3天不存在,从第7天开始迅速增加,直至达到成体脑中所见的最大值。在光学显微镜下,出生时所见的βI-PKC免疫反应性在脑干中最为强烈,在斜角带和苍白球中较强。这些神经元中的βI-PKC免疫反应性从第7天开始减弱,并在成体脑中消失,而在大脑皮层、三角隔核和脑桥核中,βI-PKC免疫反应性在出生时较弱,然后逐渐增加。βII-PKC免疫反应性在第7天首次在神经元中可见,并逐渐增加。就所检查的情况而言,βI-PKC和βII-PKC不在同一神经元中共定位。出生时βI-PKC的免疫反应性定位于生长锥样结构以及树突和胞体中。同样,α-PKC在出生时也存在于生长锥样结构中。免疫印迹分析显示,βI-PKC在出生时存在于后脑富含生长锥的部分中,但在前脑富含生长锥的部分中不存在,而α-PKC在前脑和后脑富含生长锥的部分中均有发现。在前脑或后脑富含生长锥的部分中均未检测到βII-PKC和γ-PKC。这些发现表明,βI-PKC和βII-PKC在发育的不同阶段和不同神经元中发挥作用;两种β亚型可能都参与出生后发育中的神经元功能,而只有βI-PKC在产前发育阶段的生长锥中发挥功能作用。