Radu Diana, Tomkinson Birgitta, Zachrisson Olof, Weber Günther, de Belleroche Jacqueline, Hirsch Steven, Lindefors Nils
Department of Clinical Neuroscience, Psychiatry Section, Karolinska Institutet, Stockholm, Sweden.
Brain Res. 2006 Aug 9;1104(1):175-82. doi: 10.1016/j.brainres.2006.05.059. Epub 2006 Jul 5.
Tripeptidyl peptidase II (TPPII) is a high molecular weight exopeptidase important in inactivating extracellular cholecystokinin (CCK). Our aims were to study the anatomical localization of TPPII and CCK mRNA in the Cynomolgus monkey brain as a basis for a possible functional anatomical connection between enzyme (TPPII) and substrate (CCK) and examine if indications of changes in substrate availability in the human brain might be reflected in changes of levels of TPPII mRNA.
mRNA in situ hybridization on postmortem brain from patients having had a schizophrenia diagnosis as compared to controls and on monkey and rat brain slices.
overlapping distribution patterns of mRNAs for TPPII and CCK in rat and monkey. High amounts of TPPII mRNA are seen in the neocortex, especially in the frontal region and the hippocampus. TPPII mRNA is also present in the basal ganglia and cerebellum where CCK immunoreactivity and/or CCK B receptors have been found in earlier studies, suggesting presence of CCK-ergic afferents from other brain regions. Levels of mRNAs for CCK and TPPII show a positive correlation in postmortem human cerebral cortex Brodmann area (BA) 10. TPPII mRNA might be affected following schizophrenia.
overall TPPII and CCK mRNA show a similar distribution in rat and monkey brain, confirming and extending earlier studies in rodents. In addition, correlated levels of TPPII and CCK mRNA in human BA 10 corroborate a functional link between CCK and TPPII in the human brain.
三肽基肽酶II(TPPII)是一种高分子量外肽酶,对细胞外胆囊收缩素(CCK)的失活很重要。我们的目的是研究食蟹猴脑中TPPII和CCK mRNA的解剖定位,作为酶(TPPII)和底物(CCK)之间可能存在的功能解剖学联系的基础,并研究人脑底物可用性的变化迹象是否可能反映在TPPII mRNA水平的变化中。
对诊断为精神分裂症的患者与对照组的死后大脑以及猴和大鼠脑切片进行mRNA原位杂交。
大鼠和猴中TPPII和CCK的mRNA分布模式重叠。在新皮质中可见大量TPPII mRNA,尤其是在额叶区域和海马体中。TPPII mRNA也存在于基底神经节和小脑中,早期研究在这些部位发现了CCK免疫反应性和/或CCK B受体,提示存在来自其他脑区的CCK能传入纤维。在死后人类大脑皮质布罗德曼区(BA)10中,CCK和TPPII的mRNA水平呈正相关。精神分裂症后TPPII mRNA可能会受到影响。
总体而言,TPPII和CCK mRNA在大鼠和猴脑中显示出相似的分布,证实并扩展了早期在啮齿动物中的研究。此外,人类BA 10中TPPII和CCK mRNA水平的相关性证实了人脑中CCK和TPPII之间的功能联系。