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PMID: 6381200 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Anatomic distribution of lectin-binding sites in mouse testis and epididymis.

Differentiation; research in biological diversity ·Vol. 27 ·No. 1 ·1984-00-00 ·Pages 74-81

Lee MC, Damjanov I

Abstract

Testis and epididymis of sexually mature mice were studied histochemically using 25 fluorescein-isothiocyanate-labeled lectins. Several lectin-specific binding patterns were recognized. Thus, HAA, HPA, GSA-I, and UEA-II reacted only with spermatozoa. PNA, GSA-II, SBA, VVA, BPA, RCA-I, and RCA-II reacted with spermatozoa and spermatocytes. WGA, PEA, LCA, and MPA reacted with spermatogonia, spermatocytes, and spermatozoa in increasing order of intensity. ConA, Suc. ConA, LAA, STA, LTA, LPA, PHA-E, PHA-L, UEA-I, and LBA reacted with all spermatogenic cells with equal intensity. In the epididymis, 12 lectins reacted uniformly with the epithelial cells lining all segments of this organ. One lectin (VVA) did not react with epididymal lining cells. The remaining 12 lectins reacted in a specific manner with portions of the head, body, or tail, thus selectively outlining different portions of the epididymis. RCA-I and RCA-II selectively accentuated the so-called halo cells of the epididymis. These findings provide a detailed map of lectin-binding sites in the mouse testis and epididymis and show that certain lectins can be used as specific markers for spermatogenic cells and segments of the epididymis.

MeSH Terms
Binding Sites Epididymis/metabolism,ultrastructure Fluorescent Antibody Technique Glycolipids/metabolism Glycoproteins/metabolism Lectins Male Testis/metabolism,ultrastructure
Chemicals
Glycolipids Glycoproteins Lectins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lee M C
Damjanov I
Article Info
Journal
Differentiation; research in biological diversity
Abbr.
Differentiation
ISSN
0301-4681
Published
1984-00-00
Pages
74-81
Language
English
Region
England
NLM ID
0401650
Subset
IM
Grants
NCI NIH HHS · CA23097 · United States
NIGMS NIH HHS · GM 29040 · United States
NICHD NIH HHS · HD 16437 · United States
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