Mapping and identity of cells expressing S100B protein in the brain under physiological and pathological conditions.
  Physiological Conditions Pathological Conditions
  Data from
our study
Steiner et al., 2007 Müller, 1992 Dyck et al., 1993 Boyes et al.,1986 Sathe et al., 2012 Steiner et al., 2008 Van Eldik and Griffin, 1994
TELENCEPHALON           Ø    
Frontal Cortex  ●        ●
medial orbital córtex            
cingulate cortex, area 1 Ø            
visual cortex Ø   ∆  ● ∆  ●        
Corpus callosum  ∆  ●          
Septal region   Ø Ø Ø Ø Ø Ø Ø
lateral ventricles cell ependymal ∆  ●              
lateral septal nu, dorsal part ∆  ●              
lateral septal nu, dorsal part intermédia ∆  ●              
lateral septal nu, dorsal part ventral ∆  ●              
Hippocampal region   Ø Ø Ø Ø  ●
dentate gyrus (CA4) ∆  ●              
hippocampus (CA1, CA2, CA3) ∆  ●              
Fimbria ∆  ●              
Basal nuclei region   Ø Ø Ø Ø Ø Ø
caudate nuclei ∆               
DIENCEPHALON   Ø Ø Ø Ø Ø Ø Ø
Thalamus region     Ø Ø Ø Ø Ø  
paraventricular th nu, posterior  ●              
Hipothalamus region   Ø Ø Ø Ø Ø Ø Ø
periventricular hypothamic nu ∆  ●              
3rd ventricle region ∆  ●              
ependymal cell               
BRAINSTEM   Ø Ø Ø Ø Ø ●
Substantia nigra       ●    
Pyramide ∆  ●         Ø    
Raphe nuclei region   Ø Ø Ø Ø Ø Ø Ø
pallidus raphe nu ∆  ●              
ventricle perinvetricular region  ∆ ●              
CEREBELLUM   Ø Ø Ø   Ø Ø ●
Cerebellar Cortex region                
Bergman cell            
granulosa layer ∆ ●              
Table 1: S100B cell IR: S100B IR (□); GFAP IR (Δ); Colocalization of S100B/GFAP IR(●); (Ø) not analyzed.