帕金森病
中文名称
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