Yg. Jeong et al., Ectopic expression of tyrosine hydroxylase in Zebrin II immunoreactive Purkinje cells in the cerebellum of the ataxic mutant mouse, pogo, DEV BRAIN R, 129(2), 2001, pp. 201-209
The pogo mouse is a new ataxic autosomal recessive mutant that arose in an
inbred strain (KJR/MsKist) derived from a Korean wild mouse. The phenotype
includes difficulty in maintaining normal posture and the inability to walk
straight. Several previous studies have associated inherited ataxia with t
he ectopic expression of tyrosine hydroxylase, (TH) in Purkinje cells. Ther
efore, in the present study, the distribution of TH expression was compared
with that of zebrin II in Purkinje. cells of adult pogo/pogo mutant mice.
In normal control littermates, tyrosine hydroxylase immunoreactivity is con
fined to a delicate axonal plexus ramifying through the molecular layer. In
pogo/pogo, in addition to the axonal plexus, TH-immunoreactive Purkinje ce
lls were present in all lobules of the cerebellar vermis and hemispheres, d
istributed as series parasagittal bands. The general pattern of expression
is reproducible between individuals and symmetrical about the midline. Alte
rnating stripes of TH expression are also seen in the hemispheres, and most
Purkinje cells in the paraflocculi and flocculi are immunoreactive. In pog
o/+ mice, TH-immunoreactive Purkinje cells are rare. The pattern of zebrin
II expression was used to map TH immunoreactive Purkinje cells in pogo/pogo
mutant mice. Double immunofluorescence labeling combining anti-zebrin II f
and anti-TH showed that all TH-immunoreactive Purkinje cells are zebrin II, but that many zebrin II+ Purkinje cells within a band do not stain with a
nti-TH. Taken together with the morphological changes observed in the Purki
nje cell axons, this suggests that abnormal Purkinje cell function may cont
ribute to the ataxic phenotype in pogo/pogo mice. (C) 2001 Published by Els
evier Science B.V.