REGIONALIZATION DEFECTS IN THE WEAVER MOUSE CEREBELLUM

Citation
Lm. Eisenman et al., REGIONALIZATION DEFECTS IN THE WEAVER MOUSE CEREBELLUM, Journal of comparative neurology, 394(4), 1998, pp. 431-444
Citations number
81
Categorie Soggetti
Neurosciences,Zoology
ISSN journal
00219967
Volume
394
Issue
4
Year of publication
1998
Pages
431 - 444
Database
ISI
SICI code
0021-9967(1998)394:4<431:RDITWM>2.0.ZU;2-#
Abstract
The mammalian cerebellum consists of parasagittal bands and transverse zones that are laid down early in development. When the adult cerebel lum is immunostained for the Purkinje cell-specific antigen zebrin II (i.e., aldolase C), compartmentation is reflected in alternating zebri n II+ (P+) and zebrin II- bands (P-). The zebrin II phenotype is Purki nje cell autonomous; thus, disruptions in the zebrin pattern may refle ct early problems in pattern formation. Zebrin II expression has been examined in the weaver (wv) mouse cerebellum. Both zebrin II+ and zebr in II- Purkinje cells are present in the homozygous weaver (wu/wv) mou se, but they are not distributed normally. In the posterior vermis, al though the zebrin II+ bands are wider and multilaminate, the standard compartmentation is present. However, a large zebrin II+ cell mass is absent from the central vermis, and analysis of the anterior lobe reve als several missing zebrin II+ bands. The cytoarchitectonic defects in wv mice are not simply related to the Purkinje cell abnormalities. In stead, serial reconstruction reveals two transverse boundaries-one ros trally in lobule VI and the other caudally in lobule IX-that delineate cytoarchitectonic transverse zones important in cerebellar developmen t. The abnormal zebrin expression pattern in wv/vv mice may be seconda ry to the deletion of a transverse zone. This is the first demonstrati on that Purkinje cell compartmentation can be altered by mutation; the refore, the wv mutation should prove valuable in understanding cerebel lar regionalization. J. Comp. Neurol. 394:431-444, 1998. (C) 1998 Wile y-Liss, Inc.