Homocysteine (Hcy) is a risk factor for
Alzheimer's disease (AD).
Bleomycin hydrolase (BLMH) participates in Hcy metabolism and is also linked to AD. The inactivation of the Blmh gene in mice causes accumulation of
Hcy-thiolactone in the brain and increases susceptibility to
Hcy-thiolactone-induced
seizures. To gain insight into brain-related Blmh function, we used two-dimensional IEF/SDS-PAGE gel electrophoresis and MALDI-TOF/TOF mass spectrometry to examine brain
proteomes of Blmh-/- mice and their Blmh+/+ littermates fed with a hyperhomocysteinemic high-Met or a control diet. We found that: (1)
proteins involved in brain-specific function (Ncald, Nrgn, Stmn1, Stmn2),
antioxidant defenses (Aop1), cell cycle (
RhoGDI1, Ran), and cytoskeleton assembly (Tbcb, CapZa2) were differentially expressed in brains of Blmh-null mice; (2)
hyperhomocysteinemia amplified effects of the Blmh-/- genotype on brain
protein expression; (3)
proteins involved in brain-specific function (Pebp1),
antioxidant defenses (Sod1, Prdx2, DJ-1), energy metabolism (Atp5d, Ak1, Pgam-B), and
iron metabolism (Fth) showed differential expression in Blmh-null brains only in hyperhomocysteinemic animals; (4) most
proteins regulated by the Blmh-/- genotype were also regulated by high-Met diet, albeit in the opposite direction; and (5) the differentially expressed
proteins play important roles in neural development, learning, plasticity, and aging and are linked to
neurodegenerative diseases, including AD. Taken together, our findings suggest that Blmh interacts with diverse cellular processes from energy metabolism and anti-oxidative defenses to cell cycle, cytoskeleton dynamics, and synaptic plasticity essential for normal brain homeostasis and that modulation of these interactions by
hyperhomocysteinemia underlies the involvement of Hcy in AD.