“…Fiftymicrometer-thick sections were cut on a freezing microtome and stained with either (1) luxol fast blue, (2) cresyl violet, (3) luxol fast blue with cresyl violet counterstaining (K lüver and Barrera stain), or (4) hematoxylin and eosin. Immunocytochemistry was performed according to standard protocols at antibody dilutions recommended by the manufacturer using primary antisera directed against the following: Schwann cells (Schwann /2E) (Dr. Y. Nakazato, Gunma University, Gunma, Japan) (Arai et al, 1998); protein P zero (P 0 ) (Dr. J. Archelos, Karl-Franzens-University, Graz, Austria); p75 neurotrophin receptor (p75) (Dr. L. Reichardt, University of C alifornia, San Francisco, CA); glial fibrillary acidic protein (GFAP; Roche-Boehringer, Indianapolis, I N; C lone G-A-5); oligodendrocytes (M AB1580) (Chemicon, Temecula, CA,); OX-8, San Diego,CA); ED1 (Serotec, Raleigh, NC); C TB (List Biologic, C ampbell, CA); or saporin (Advanced Targeting Systems). We found that the Schwann /2E and P 0 antibodies produced equivalent staining, and therefore both antibodies were used to identif y myelinating Schwann cells.…”