Overlapping functions of the cell adhesion molecules Nr-CAM and L1 in cerebellar granule cell development

Takeshi Sakurai(Rutgers, The State University of New Jersey), Marc Lustig(Columbia University Irving Medical Center), Joanne Babiarz(Rutgers, The State University of New Jersey), Andrew J. Furley(University of Sheffield), Steven Tait(University of Edinburgh), Peter Brophy(University of Edinburgh), Stephen Brown(Columbia University), Lucia Brown(Columbia University), Carol A. Mason(Columbia University), Martin Grumet(Rutgers, The State University of New Jersey)
The Journal of Cell Biology
September 17, 2001
Cited by 108Open Access
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Abstract

The structurally related cell adhesion molecules L1 and Nr-CAM have overlapping expression patterns in cerebellar granule cells. Here we analyzed their involvement in granule cell development using mutant mice. Nr-CAM-deficient cerebellar granule cells failed to extend neurites in vitro on contactin, a known ligand for Nr-CAM expressed in the cerebellum, confirming that these mice are functionally null for Nr-CAM. In vivo, Nr-CAM-null cerebella did not exhibit obvious histological defects, although a mild size reduction of several lobes was observed, most notably lobes IV and V in the vermis. Mice deficient for both L1 and Nr-CAM exhibited severe cerebellar folial defects and a reduction in the thickness of the inner granule cell layer. Additionally, anti-L1 antibodies specifically disrupted survival and maintenance of Nr-CAM-deficient granule cells in cerebellar cultures treated with antibodies. The combined results indicate that Nr-CAM and L1 play a role in cerebellar granule cell development, and suggest that closely related molecules in the L1 family have overlapping functions.


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