Interaction of the human epididymal protein CD52 (HE5) with epididymal spermatozoa from men and cynomolgus monkeys

A monoclonal antibody (CAMPATH‐1G) against the human lymphocyte surface protein CD52, which is similar to the epididymal secretion HE5, was used to ascertain the presence of this protein on maturing primate spermatozoa by flow cytometry. The percentage of human viable spermatozoa stained specifically with this antibody increased from sperm in spermatocoeles (0.5%), to the efferent ducts (3.8%), corpus (47.2%), and cauda (85.7%) epididymidis. Positive cells revealed staining mainly over the whole tail and postacrosomal region of the sperm head. Spermatozoa (∼10%) from both the efferent ducts and corpus epididymidis took up additional antigen when incubated with human distal cauda epididymidal plasma as a source of CD52, and 12–22% of human testicular sperm (from spermatocoeles) took up CD52 from human seminal plasma. In the cynomolgus monkey, nonspecific binding of control IgG was greater than that in human males and net CD52 staining was measurable only on ∼30% of corpus sperm where it was mainly on the principal piece. Neither caput nor cauda sperm took up human CD52 upon incubation with human seminal plasma, but an additional 27% of corpus sperm expressed CD52. Such uptake of CD52 was drastically reduced, or did not occur, when seminal plasma had been fractionated by filtration through 0.1 μm filters (filtrate II) or 300,000 Da cutoff filters (filtrate III), respectively. Western blots revealed that CD52 contents were much reduced in filtrate II and nondetectable in filtrate III of seminal plasma. Similar reduction of CD52 in the filtrate of cauda epididymidal plasma indicates the association of this epididymal secretion with large molecular factors and suggests their involvement as carriers in the in vivo transfer of the secretion onto the epididymal sperm surface. The in vitro uptake of CD52 by some but not all immature sperm and the detection by Western blotting of much less CD52 in the corpus than the cauda luminal plasma suggest that the acquisition of this epididymal secretion by spermatozoa depends on their maturation status as well as the availability of the protein in the epididymal lumen. Mol. Reprod. Dev. 48:267–275, 1997. © 1997 Wiley‐Liss, Inc.

[1]  M. Nishihara,et al.  Different female reproductive phenotypes determined by human growth hormone (hGH) levels in hGH-transgenic rats. , 1997, Biology of reproduction.

[2]  G. Weinbauer,et al.  Maturation of monkey spermatozoa in the epididymis with respect to their ability to undergo the acrosome reaction. , 1996, Journal of andrology.

[3]  C. Hale,et al.  Recognition of CD52 allelic gene products by CAMPATH‐1H antibodies , 1996, Immunology.

[4]  G. Primus,et al.  The monoclonal antibody GZS-1 detects a maturation-associated antigen of human spermatozoa that is also present on the surface of human mononuclear blood cells. , 1996, Journal of reproductive immunology.

[5]  J. Tesarik,et al.  Regulators of sperm function , 1996 .

[6]  J. Morrell,et al.  Maturation of sperm motility in the epididymis of the common marmoset (Callithrix jacchus) and the cynomolgus monkey (Macaca fascicularis). , 1996, International journal of andrology.

[7]  J. Atkinson,et al.  GPI-anchored complement regulatory proteins in seminal plasma. An analysis of their physical condition and the mechanisms of their binding to exogenous cells. , 1996, The Journal of clinical investigation.

[8]  C. Kirchhoff,et al.  Molecular cloning and characterization of HE1, a major secretory protein of the human epididymis. , 1996, Biology of reproduction.

[9]  G. Hale,et al.  Cell-to-cell transfer of glycosylphosphatidylinositol-anchored membrane proteins during sperm maturation. , 1996, Molecular human reproduction.

[10]  C. Kirchhoff CD52 is the 'major maturation-associated' sperm membrane antigen. , 1996, Molecular human reproduction.

[11]  G. Hale Synthetic peptide mimotope of the CAMPATH-1 (CD52) antigen, a small glycosylphosphatidylinositol-anchored glycoprotein. , 1995, Immunotechnology : an international journal of immunological engineering.

[12]  J. Platt,et al.  In vivo transfer of GPI-linked complement restriction factors from erythrocytes to the endothelium. , 1995, Science.

[13]  S. Meri,et al.  High-density lipoproteins can act as carriers of glycophosphoinositol lipid-anchored CD59 in human plasma. , 1994, Immunology.

[14]  E. Nieschlag,et al.  Changes in movement characteristics of human spermatozoa along the length of the epididymis. , 1993, Biology of reproduction.

[15]  M. Ferguson,et al.  Structure of the CAMPATH-1 antigen, a glycosylphosphatidylinositol-anchored glycoprotein which is an exceptionally good target for complement lysis. , 1993, The Biochemical journal.

[16]  J. Atkinson,et al.  Physiologic relevance of the membrane attack complex inhibitory protein CD59 in human seminal plasma: CD59 is present on extracellular organelles (prostasomes), binds cell membranes, and inhibits complement- mediated lysis , 1993, The Journal of experimental medicine.

[17]  I. Lauder,et al.  The glycosylphosphatidylinositol-anchored lymphocyte antigen CDw52 is associated with the epididymal maturation of human spermatozoa. , 1993, Journal of reproductive immunology.

[18]  R. Ivell,et al.  Region‐specific variation of gene expression in the human epididymis as revealed by in situ hybridization with tissue‐specific cDNAs , 1993, Molecular reproduction and development.

[19]  R. Ivell,et al.  A major mRNA of the human epididymal principal cells, HE5, encodes the leucocyte differentiation CDw52 antigen peptide backbone , 1993, Molecular reproduction and development.

[20]  L. Hall,et al.  Identification of an abundant monkey epididymal transcript encoding a homologue of human CAMPATH-1 antigen precursor. , 1992, Biochimica et biophysica acta.

[21]  A. Bernard,et al.  The distribution of the CDW52 molecule on blood cells and characterization of its involvement in T cell activation. , 1992, Transplantation.

[22]  M. Bergmann,et al.  Organization of tubules in the human caput epididymidis and the ultrastructure of their epithelia. , 1991, The American journal of anatomy.

[23]  L. Packman,et al.  Characterization of the CAMPATH‐1 (CDw52) antigen: biochemical analysis and cDNA cloning reveal an unusually small peptide backbone , 1991, European journal of immunology.

[24]  D. Koppel,et al.  Evidence that proteolysis of the surface is an initial step in the mechanism of formation of sperm cell surface domains , 1990, The Journal of cell biology.

[25]  G. Hale,et al.  The CAMPATH-1 antigen (CDw52). , 1990, Tissue antigens.

[26]  H. Waldmann,et al.  REMISSION INDUCTION IN NON-HODGKIN LYMPHOMA WITH RESHAPED HUMAN MONOCLONAL ANTIBODY CAMPATH-1H , 1988, The Lancet.

[27]  C. Carron,et al.  Epididymal maturation and the acrosome reaction in mouse sperm: response to zona pellucida develops coincident with modification of M42 antigen. , 1988, Biology of reproduction.

[28]  G. Olson,et al.  Characterization of maturation-dependent extrinsic proteins of the rat sperm surface , 1985, The Journal of cell biology.

[29]  G Scalise,et al.  Letter: Australia antigen in urine. , 1973, The Lancet.