TY - JOUR
T1 - Lewis X-containing neoglycoproteins mimic the intrinsic ability of zona pellucida glycoprotein ZP3 to induce the acrosome reaction in capacitated mouse sperm
AU - Hanna, William F.
AU - Kerr, Candace L.
AU - Shaper, Joel H.
AU - Wright, William W.
PY - 2004/9
Y1 - 2004/9
N2 - The binding of zona pellucida (ZP) glycoprotein ZP3 to mouse sperm surface receptors is mediated by protein-carbohydrate interactions. Subsequently, ZP3 induces sperm to undergo the acrosome reaction, an obligatory step in fertilization. We have previously identified Lewis X (Lex; Galβ4[Fucα3] GlcNAc) as a potent inhibitor of in vitro sperm-ZP binding (Johnston et al. J Biol Chem 1998; 273:1888-1895). This glycan is recognized by ∼70% of the ZP3 binding sites on capacitated, acrosome-intact mouse sperm, whereas Lewis A (Lea; Galβ3[Fucα4]GlcNAc) is recognized by most of the remaining sites (Kerr et al. Biol Reprod 2004; 71:770-777). Herein, we test the hypothesis that Lex- and Le a-containing glycans, when clustered on a neoglycoprotein, bind ZP3 receptors on sperm and induce sperm to undergo the acrosome reaction via the same signaling pathways as ZP3. Results show that a Lex-containing neoglycoprotein induced the acrosome reaction in a dose-dependent and capacitation-dependent manner. A Lea-containing neoglycoprotein also induced sperm to undergo the acrosome reaction but was less potent than Le x-containing neoglycoproteins. In contrast, neoglycoproteins containing β4-lactosamine (Galβ4GlcNAc), Lewis B (Fucα2Galβ 3[Fucα4]GlcNAc), and sialyl-Lex glycans were inactive, as were four other neoglycoproteins with different nonfucosylated glycans. Consistent with these results, unconjugated Lex- and Lea-capped glycans were dose-dependent inhibitors, which at saturation, reduced the ZP-induced acrosome reaction by about 60% and 30%, respectively. Experiments utilizing pharmacological inhibitors suggest that induction of the acrosome reaction by solubilized ZP and Lex- and Lea-containing neoglycoproteins require the same calcium-dependent pathway. However, only the ZP-induced acrosome reaction requires a functional Gi protein. Thus, Lex-containing neoglycoproteins bind to a major class of ZP3 receptors on capacitated sperm. A Lea-containing neoglycoprotein binds a second ZP3 receptor but is a less-potent inducer of the acrosome reaction.
AB - The binding of zona pellucida (ZP) glycoprotein ZP3 to mouse sperm surface receptors is mediated by protein-carbohydrate interactions. Subsequently, ZP3 induces sperm to undergo the acrosome reaction, an obligatory step in fertilization. We have previously identified Lewis X (Lex; Galβ4[Fucα3] GlcNAc) as a potent inhibitor of in vitro sperm-ZP binding (Johnston et al. J Biol Chem 1998; 273:1888-1895). This glycan is recognized by ∼70% of the ZP3 binding sites on capacitated, acrosome-intact mouse sperm, whereas Lewis A (Lea; Galβ3[Fucα4]GlcNAc) is recognized by most of the remaining sites (Kerr et al. Biol Reprod 2004; 71:770-777). Herein, we test the hypothesis that Lex- and Le a-containing glycans, when clustered on a neoglycoprotein, bind ZP3 receptors on sperm and induce sperm to undergo the acrosome reaction via the same signaling pathways as ZP3. Results show that a Lex-containing neoglycoprotein induced the acrosome reaction in a dose-dependent and capacitation-dependent manner. A Lea-containing neoglycoprotein also induced sperm to undergo the acrosome reaction but was less potent than Le x-containing neoglycoproteins. In contrast, neoglycoproteins containing β4-lactosamine (Galβ4GlcNAc), Lewis B (Fucα2Galβ 3[Fucα4]GlcNAc), and sialyl-Lex glycans were inactive, as were four other neoglycoproteins with different nonfucosylated glycans. Consistent with these results, unconjugated Lex- and Lea-capped glycans were dose-dependent inhibitors, which at saturation, reduced the ZP-induced acrosome reaction by about 60% and 30%, respectively. Experiments utilizing pharmacological inhibitors suggest that induction of the acrosome reaction by solubilized ZP and Lex- and Lea-containing neoglycoproteins require the same calcium-dependent pathway. However, only the ZP-induced acrosome reaction requires a functional Gi protein. Thus, Lex-containing neoglycoproteins bind to a major class of ZP3 receptors on capacitated sperm. A Lea-containing neoglycoprotein binds a second ZP3 receptor but is a less-potent inducer of the acrosome reaction.
KW - Acrosome reaction
KW - Fertilization
KW - Gamete biology
KW - Sperm
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U2 - 10.1095/biolreprod.103.023820
DO - 10.1095/biolreprod.103.023820
M3 - Article
C2 - 15128591
AN - SCOPUS:4243077563
SN - 0006-3363
VL - 71
SP - 778
EP - 789
JO - Biology of Reproduction
JF - Biology of Reproduction
IS - 3
ER -