Complementary stripes of phospholipase Cbeta3 and Cbeta4 expression by Purkinje cell subsets in the mouse cerebellum

J Comp Neurol. 2006 May 20;496(3):303-13. doi: 10.1002/cne.20912.

Abstract

Transverse boundaries divide the cerebellar cortex into four transverse zones, and within each zone the cortex is further subdivided into a symmetrical array of parasagittal stripes. Several molecules believed to mediate long-term depression at the parallel fiber-Purkinje cell synapse are known to be expressed in stripes. We have therefore explored the distributions of phospholipase Cbeta3 and phospholipase Cbeta4, key components in the transduction of type 1 metabotropic glutamate receptor-mediated responses. The data reveal that both phospholipase Cbeta isotypes are expressed strongly in the mouse cerebellum in subsets of Purkinje cells. The two distributions are distinct and largely nonoverlapping. The pattern of phospholipase Cbeta3 expression is unique, revealing stripes in three of the four transverse zones and a uniform distribution in the fourth. In contrast, phospholipase Cbeta4 appears to be confined largely to the Purkinje cells that are phospholipase Cbeta3-negative. PLCbeta3 is restricted to the zebrin II-immunopositive Purkinje cell subset. Not all zebrin II-immunoreactive Purkinje cells express PLCbeta3: in lobules IX and X it is restricted to that zebrin II-immunopositive subset that also expresses the small heat shock protein HSP25. PLCbeta4 expression is restricted to, and coextensive with, the zebrin II-immunonegative Purkinje cell subset. These nonoverlapping expression patterns suggest that long-term depression may be manifested differently between cerebellar modules.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western / methods
  • Cerebellum / cytology*
  • Gene Expression / physiology*
  • Heat-Shock Proteins / metabolism
  • Immunohistochemistry / methods
  • Isoenzymes / metabolism*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Models, Anatomic
  • Molecular Chaperones
  • Neoplasm Proteins / metabolism
  • Nerve Tissue Proteins / metabolism
  • Phospholipase C beta
  • Purkinje Cells / classification
  • Purkinje Cells / enzymology*
  • Type C Phospholipases / metabolism*

Substances

  • Heat-Shock Proteins
  • Hsbp1 protein, mouse
  • Isoenzymes
  • Molecular Chaperones
  • Neoplasm Proteins
  • Nerve Tissue Proteins
  • zebrin II
  • Type C Phospholipases
  • Phospholipase C beta