Skip to main content
. 2020 Oct 31;53(10):500–511. doi: 10.5483/BMBRep.2020.53.10.158

Table 2.

The 14-3-3γ in brain disorders

Category of disease Name of disease Expression pattern or potential role in disease References
Neurodevelopmental disorders Williams syndrome Associated with epilepsy phenotypes 54-57
Down syndrome (DS) Decreased in the cortex of fetal DS patients 63
Increased in the cortex of aged DS patients 62
Neurodegenerative disorders Parkinson’s disease (PD) Colocalized with the Lewy body of PD 70-72
Decreased in the transgenic a-syn mouse 73
Neuroprotection against the rotenone or MPTP induced cytotoxicity 74
Promote the a-syn aggregation 75, 76
Alzheimer’s disease (AD) Colocalized with the NFT in hippocampus of AD patients 83
Increased in overall cortical regions of aged AD patients 84
Decreased in the frontal cortex of postmortem AD patients 85
Creutzfeldt-Jakob disease (CJD) Useful marker for CJD diagnosis using CSF 88-95
Neuroinflammatory disease Inflammatory joint disease (IJD) Highly observed in SF and serum of patients with IJD 96
Cruciate ligament rupture (CCLR) A marker for osteoarthritis caused by CCLR 97
Multiple sclerosis (MS) Increased in the spinal cord of chronic MOG-EAE 98
A protective factor for OL against autoimmune dehydration 98
Ischemic damaged brain Increased in infarct lesions of ischemic brain 102, 103
Detected in CSF of MELAS patients 104
A survival factor for ischemic-induced cell death in neurons 106-108
A protectant against ischemic cortical astrocytes 109-115
CNS cancer Glioma Promote glioblastoma progression 126-128

The 14-3-3γ is implicated in neurodegenerative and neurodevelopmental disorders, and is also associated with neuroinflammatory diseases and CNS cancer such as glioma. The 14-3-3γ is likely to be involved in the development of various brain diseases, and is useful as a biomarker for diagnosis and a potential therapeutic target for treatment. (α-syn: α-synuclein; NFT: neurofibrillary tangles; SF: synovial fluid; CSF: cerebrospinal fluid; CCLR: cranial cruciate ligament rupture; MOG-EAE: murine myelin oligodendrocyte-induced experimental autoimmune encephalomyelitis; OL: oligodendrocyte; MELAS: mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes).