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Parkinson disease

KEGG ID: hsa05012

中文名称

帕金森病

通路描述

帕金森病(PD)是一种进行性神经退行性运动障碍,主要源于黑质致密部(SNc)多巴胺能(DA)神经元的死亡。环境因素和家族帕金森病关联基因的突变(如 SNCA、Parkin、DJ-1、PINK1 和 LRRK2)与 PD 发病机制相关。这些致病突变和环境因素已知通过氧化应激、细胞内 Ca2+ 稳态失调、线粒体功能障碍和蛋白质处理改变损害 DA 神经元的关键功能和生存。SNc 中 DA 神经元的死亡导致多巴胺能输入到纹状体下降,这被认为是通过诱导基底节中直接(dSPNs)和间接(iSPNs)通路中纹状体锥体投射神经元(SPNs)的假性低活性和高活性来阻碍运动的。
英文描述
Parkinson disease (PD) is a progressive neurodegenerative movement disorder that results primarily from the death of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc). Both environmental factors and mutations in familial PD-linked genes such as SNCA, Parkin, DJ-1, PINK1 and LRRK2 are associated with PD pathogenesis. These pathogenic mutations and environmental factors are known to cause disease due to oxidative stress, intracellular Ca2+ homeostasis impairment, mitochondrial dysfunctions and altered protein handling compromising key roles of DA neuronal function and survival. The demise of DA neurons located in the SNc leads to a drop in the dopaminergic input to the striatum, which is hypothesized to impede movement by inducing hypo and hyper activity in striatal spiny projection neurons (SPNs) of the direct (dSPNs) and indirect (iSPNs) pathways in the basal ganglia, respectively.

所含基因

268 个基因
ADCY5 ADORA2A ADRM1 APAF1 ATF4 ATF6 ATP5F1A ATP5F1B ATP5F1C ATP5F1D ATP5F1E ATP5MC1 ATP5MC2 ATP5MC3 ATP5PB ATP5PD ATP5PF ATP5PO ATP6 ATP8 BAX BCL2L1 CALM1 CALM2 CALM3 CALML3 CALML4 CALML5 CALML6 CAMK2A CAMK2B CAMK2D CAMK2G CASP3 CASP9 COX1 COX2 COX3 COX4I1 COX4I2 COX5A COX5B COX6A1 COX6A2 COX6B1 COX6B2 COX6C COX7A1 COX7A2 COX7A2L COX7B COX7B2 COX7C COX8A COX8C COXFA4 COXFA4L2 CYC1 CYCS CYTB DAXX DDIT3 DRD1 DRD2 DUSP1 EIF2AK3 EIF2S1 ERN1 GNAI1 GNAI2 GNAI3 GNAL GNAS GPR37 HSPA5 HTRA2 ITPR1 ITPR2 ITPR3 KEAP1 KIF5A KIF5B KIF5C KLC1 KLC2 KLC3 KLC4 LOC107984365 LRRK2 MAOA MAOB MAP3K5 MAPK10 MAPK8 MAPK9 MAPT MCU MFN1 MFN2 ND1 ND2 ND3 ND4 ND4L ND5 ND6 NDUFA1 NDUFA10 NDUFA11 NDUFA12 NDUFA13 NDUFA2 NDUFA3 NDUFA5 NDUFA6 NDUFA7 NDUFA8 NDUFA9 NDUFAB1 NDUFB1 NDUFB10 NDUFB11 NDUFB2 NDUFB3 NDUFB4 NDUFB5 NDUFB6 NDUFB7 NDUFB8 NDUFB9 NDUFC1 NDUFC2 NDUFC2-KCTD14 NDUFS1 NDUFS2 NDUFS3 NDUFS4 NDUFS5 NDUFS6 NDUFS7 NDUFS8 NDUFV1 NDUFV2 NDUFV3 NFE2L2 PARK7 PINK1 PLCG1 PPIF PRKACA PRKACB PRKACG PRKN PSMA1 PSMA2 PSMA3 PSMA4 PSMA5 PSMA6 PSMA7 PSMA8 PSMB1 PSMB2 PSMB3 PSMB4 PSMB5 PSMB6 PSMB7 PSMC1 PSMC2 PSMC3 PSMC4 PSMC5 PSMC6 PSMD1 PSMD11 PSMD12 PSMD13 PSMD14 PSMD2 PSMD3 PSMD4 PSMD6 PSMD7 PSMD8 PSMD9 RPS27A RYR3 SDHA SDHB SDHC SDHD SEM1 SEPTIN5 SLC11A2 SLC18A1 SLC18A2 SLC25A31 SLC25A4 SLC25A5 SLC25A6 SLC39A1 SLC39A10 SLC39A11 SLC39A12 SLC39A13 SLC39A14 SLC39A2 SLC39A3 SLC39A4 SLC39A5 SLC39A6 SLC39A7 SLC39A8 SLC39A9 SLC6A3 SNCA SNCAIP SOD1 TH TP53 TRAP1 TUBA1A TUBA1B TUBA1C TUBA3C TUBA3D TUBA3E TUBA4A TUBA8 TUBAL3 TUBB TUBB1 TUBB2A TUBB2B TUBB3 TUBB4A TUBB4B TUBB6 TUBB8 TUBB8B TXN TXN2 UBA1 UBA52 UBA7 UBB UBC UBE2G1 UBE2G2 UBE2J1 UBE2J2 UBE2L3 UBE2L6 UCHL1 UQCR10 UQCR11 UQCRB UQCRC1 UQCRC2 UQCRFS1 UQCRH UQCRHL UQCRQ VDAC1 VDAC2 VDAC3 XBP1