TY - JOUR
T1 - Distribution of Ca2+/calmodulin-dependent protein kinase I beta 2 in the central nervous system of the rat
AU - Rina-Susilowati,
AU - Aulia, Ahmad
AU - Sakagami, Hiroyuki
AU - Kikkawa, Satoshi
AU - Kondo, Hisatake
AU - Minami, Yasuhiro
AU - Terashima, Toshio
PY - 2001/8/17
Y1 - 2001/8/17
N2 - Recently, we reported the mRNA localization of Ca2+/calmodulin-dependent protein kinase I beta 2 isoform (CaMKIβ2) in the mouse nervous system. In the present study, polyclonal antibody against CaMKIβ2 was generated and used to investigate the distribution of the enzyme within the central nervous system of the rat. Interestingly some differences were observed between the enzyme localization and previous mRNA detection [J. Neurochem. 268 (1999) 26512]. The strongest expression of the enzyme was found in pontine nuclei. Immunopositive fibers could be traced through the middle cerebellar peduncle until they reached the cerebellum. Quite strong staining could also be observed in almost all of the neurons in the neocortex, hippocampus, amygdala, hypothalamus, brainstem and cerebellum, including the nuclei of the cranial nerves and Purkinje cell layer of the cerebellar cortex which was not clearly detected in the previous in situ hybridization study. In the spinal cord, CaMKIβ2 could be detected in the gray matter with stronger expression in the dorsal horn. CaMKIβ2 showed very strong nuclear localization but was also present in the cytoplasm of some neurons. Such localization suggests that CaMKIβ2 may be involved in many neuronal functions in the central nervous system, including the possibility of important roles in nuclear signal transduction.
AB - Recently, we reported the mRNA localization of Ca2+/calmodulin-dependent protein kinase I beta 2 isoform (CaMKIβ2) in the mouse nervous system. In the present study, polyclonal antibody against CaMKIβ2 was generated and used to investigate the distribution of the enzyme within the central nervous system of the rat. Interestingly some differences were observed between the enzyme localization and previous mRNA detection [J. Neurochem. 268 (1999) 26512]. The strongest expression of the enzyme was found in pontine nuclei. Immunopositive fibers could be traced through the middle cerebellar peduncle until they reached the cerebellum. Quite strong staining could also be observed in almost all of the neurons in the neocortex, hippocampus, amygdala, hypothalamus, brainstem and cerebellum, including the nuclei of the cranial nerves and Purkinje cell layer of the cerebellar cortex which was not clearly detected in the previous in situ hybridization study. In the spinal cord, CaMKIβ2 could be detected in the gray matter with stronger expression in the dorsal horn. CaMKIβ2 showed very strong nuclear localization but was also present in the cytoplasm of some neurons. Such localization suggests that CaMKIβ2 may be involved in many neuronal functions in the central nervous system, including the possibility of important roles in nuclear signal transduction.
KW - CaM-kinase I
KW - Central nervous system
KW - Immunohistochemistry
KW - Rat
UR - http://www.scopus.com/inward/record.url?scp=0035903056&partnerID=8YFLogxK
U2 - 10.1016/S0006-8993(01)02440-4
DO - 10.1016/S0006-8993(01)02440-4
M3 - Article
C2 - 11489438
AN - SCOPUS:0035903056
SN - 0006-8993
VL - 911
SP - 1
EP - 11
JO - Brain Research
JF - Brain Research
IS - 1
ER -