A Heme Oxygenase-1 Transducer Model of Degenerative and Developmental Brain Disorders

作者：Schipper, Hyman M.^*; Song, Wei

来源：International Journal of Molecular Sciences, 2015, 16(3): 5400-5419.

DOI：10.3390/ijms16035400

• MITOCHONDRIAL IRON SEQUESTRATION
• OXIDATIVE STRESS
• CORPORA-AMYLACEA
• ALZHEIMERS-DISEASE
• OVER-EXPRESSION
• GENE-EXPRESSION
• CARBON-MONOXIDE
• OVEREXPRESSION
• SCHIZOPHRENIA
• DEPOSITION

Heme oxygenase-1 (HO-1) is a 32 kDa protein which catalyzes the breakdown of heme to free iron, carbon monoxide and biliverdin. The Hmox1 promoter contains numerous consensus sequences that render the gene exquisitely sensitive to induction by diverse pro-oxidant and inflammatory stimuli. In "stressed" astroglia, HO-1 hyperactivity promotes mitochondrial iron sequestration and macroautophagy and may thereby contribute to the pathological iron deposition and bioenergetic failure documented in Alzheimer disease, Parkinson disease and certain neurodevelopmental conditions. Glial HO-1 expression may also impact neuroplasticity and cell survival by modulating brain sterol metabolism and the proteasomal degradation of neurotoxic proteins. The glial HO-1 response may represent a pivotal transducer of noxious environmental and endogenous stressors into patterns of neural damage and repair characteristic of many human degenerative and developmental CNS disorders.

• 出版日期2015-3
• 单位河北医科大学