
In mammals, Ca2+and\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} \begin{equation*}{\mathrm{HCO}}_{3}^{-}\end{equation*}\end{document}ions play a critical role in the regulation of sperm function, most likely by regulation of cAMP levels. Mammalian germ cells contain a soluble adenylyl cyclase (sAC) with properties distinct from the well characterized membrane-bound enzymes Here we investigated whether the cyclase expressed in mature spermatozoa has the properties of sAC and whether it is regulated by Ca2+. In addition to an\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} \begin{equation*}{\mathrm{HCO}}_{3}^{-}\end{equation*}\end{document}-dependent activation, the cyclase endogenous to human spermatozoa is stimulated 2- to 3-fold by Ca2+in a concentration-dependent manner (EC50≈ 400 nM). In a similar fashion, Ca2+activates the recombinant rat and human full-length sAC with similar EC50values. The Ca2+stimulation was also observed when sAC was activated with\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} \begin{equation*}{\mathrm{HCO}}_{3}^{-}\end{equation*}\end{document}, was independent of calmodulin, and was associated with an increase inVmaxwithout changes inKmfor ATP-Mg2+. An increase in intracellular Ca2+by ionophore or by a muscarinic cholinergic receptor agonist increases cAMP in cells transfected with FL-hsAC, but not in mock-transfected cells. Similarly, both Ca2+and\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} \begin{equation*}{\mathrm{HCO}}_{3}^{-}\end{equation*}\end{document}stimulate cAMP accumulation in human spermatozoa. These findings provide evidence that human spermatozoa express a cyclase with the properties of sAC and that Ca2+can substitute for\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} \begin{equation*}{\mathrm{HCO}}_{3}^{-}\end{equation*}\end{document}in the stimulation of this enzyme, underscoring an important role for sAC in the control of sperm functions.
Male, Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Molecular Sequence Data, Spermatozoa, Recombinant Proteins, Rats, Solubility, Animals, Humans, Calcium, Adenylyl Cyclases, DNA Primers
Male, Base Sequence, Reverse Transcriptase Polymerase Chain Reaction, Molecular Sequence Data, Spermatozoa, Recombinant Proteins, Rats, Solubility, Animals, Humans, Calcium, Adenylyl Cyclases, DNA Primers
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