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This Article Full Text Full Text (PDF) All Versions of this Article: 68/1/51    most recent biolreprod.102.006361v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Dettin, L. Articles by Maldonado, C. A. Search for Related Content PubMed PubMed Citation Articles by Dettin, L. Articles by Maldonado, C. A. Agricola Articles by Dettin, L. Articles by Maldonado, C. A.

Regulated Expression and Ultrastructural Localization of Galectin-1, a Proapoptotic ß-Galactoside-Binding Lectin, During Spermatogenesis in Rat Testis¹

^a Center of Electron Microscopy, School of Medical Sciences, National University of Cordoba, C.P. 5000, Córdoba, Argentina ^b Division of Immunogenetics, School of Medicine, University of Buenos Aires, C.P. 1120, Buenos Aires, Argentina

Galectin-1, a highly conserved ß-galactoside-binding protein, induces apoptosis of activated T cells and suppresses the development of autoimmunity and chronic inflammation. To gain insight regarding the potential role of galectin-1 as a novel mechanism of immune privilege, we investigated expression and ultrastructural localization of galectin-1 in rat testis. Galectin-1 expression was assessed by Western blot analysis and immunocytochemical localization in testes obtained from rats aged from 9 to 60 days. Expression of this carbohydrate-binding protein was developmentally regulated, and its immunolabeling exhibited a stage-specific pattern throughout the spermatogenic process. Immunogold staining using the anti-galectin-1 antibody revealed the typical Sertoli cell profile in the seminiferous epithelium, mainly at stages X–II. During spermiation (stages VI–VIII), a strong labeling was observed at the luminal pole of seminiferous epithelium, localized on apical stalks of Sertoli cells, on heads of mature spermatids, and on bodies of residual cytoplasm. Moreover, spermatozoa released into the lumen showed a strong immunostaining. Following spermiation (stage VIII), galectin-1 expression was restored at the basal portion of Sertoli cells and progressively spread out through the whole cells as differentiation of germinal cells proceeded. Immunoelectron microscopy confirmed distribution of galectin-1 in nuclei and cytoplasmic projections of Sertoli cells and on heads and tails of late spermatids and residual bodies. Surface localization of galectin-1 was evidenced in spermatozoa from caput epididymis. Thus, the regulated expression of galectin-1 during the spermatogenic cycle suggests a novel role for this immunosuppressive lectin in reproductive biology.

¹ Supported by grants from Fundación Sales, Fundación Roemmers, and Fundación Antorchas (early career grant) to G.A.R and from Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) to C.A.M.

² Correspondence: Cristina Maldonado, Centro de Microscopía Electrónica, Facultad de Ciencias Médicas, Universidad Nacional de Córdoba, Casilla Postal 362, 5000 Córdoba, Argentina. FAX: 54351 4333021; cmaldon{at}cmefcm.uncor.edu

³ G.A.R. and C.A.M. contributed equally to this work