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  • 1
    UID:
    almahu_9947381965602882
    Format: 1 online resource (185 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889195060
    Series Statement: Frontiers Research Topics
    Content: The development of the field of membrane guanylate cyclase transduction system has been colorful, filled with exceptional historical events in cellular signaling research. From denial to resurgence, the field has branched in multiple directions. The signal transduction characteristics and signaling elements are unique. The field has established cyclic GMP as an ubiquitous intracellular second messenger, playing a critical role in the control of many physiological processes, including cardiac vasculature, smooth muscle relaxation, blood volume, cellular growth, sensory transduction, neural plasticity, learning and memory. Unlike the three-component design of its predecessor: adenylate cyclase, G-protein and G-protein coupled receptor, the membrane guanylate cyclase transduction system consists of a single entity, a trans-membrane-spanning protein that serves as both a receptor and a signal transducer. Membrane guanylate cyclases exist in multiple forms. Each form translates the captured signal at a structurally conserved core catalytic site that resides in the intracellular domain. Yet the mechanism of capturing the signal is unique to each form. The surface receptor form uses its extracellular domain to capture hormonal signals; the Ca2+-modulated ROS-GC employs its intracellular domains; and the olfactory receptor ONE-GC captures odorant signals at its extracellular domain and amplifies them at multiple intracellular domains. The composition of the hormone receptor form differs from the ROS-GC and ONE-GC forms, consisting of a single polypeptide, that is both a signal receptor and the transducer. In contrast, both ROS-GC and ONE-GC are multi-component systems. A Ca2+ sensing subunit(s) captures the signal and transmits it to a companion guanylate cyclase, that transduces it. Moreover, the modes of signal transduction vary in ROS-GC and ONE-GC. ROS-GC is a direct transducer of Ca2+ signals but the Ca2+ sensors in ONE-GC only amplify the odorant signal received and transmitted by its extracellular domain. An additional refinement is that ROS-GC1 is a bimodal Ca2+ switch, turned “OFF” as intracellular [Ca2+] rises above 75 nM, but then turned back “ON” when [Ca2+] exceeds 345 nM. These modes occur uniquely in the outer segments and synapses of cones in rodent retinas. In a new paradigm change, the dogma has been shattered that the ANF hormone receptor guanylate cyclase, ANF-RGC, is the specific transducer of ANF alone. It is now known that ANF-RGC also transduces a Ca2+ signal. Ca2+ captured by its sensor neurocalcin δ (NCδ) directly activates the catalytic module of ANF-RGC. Accordingly, and impressively, targeted gene-deletion mouse model studies demonstrate that both pathways are linked with blood pressure regulation. Their disruption causes hypertension. Thus the ANF-RGC combines features of hormone receptor and ROS-GC forms of membrane guanylate cyclases. These studies also broaden the classification of the Ca2+ sensors. NCδ, classified as a neuronal calcium sensor, is more widespread. The general theme of this Research Topic is to present a comprehensive coverage of the expanding role being played by this beautifully designed transduction machinery. The reviews will cover its history to its present status, move on to theoretical and experimental investigations propelling the field in future directions, and provide illustrations where the field contributes to clinical medicine.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    UID:
    gbv_1778630499
    Format: 1 Online-Ressource (185 p.)
    ISBN: 9782889195060
    Series Statement: Frontiers Research Topics
    Content: The tale of cyclic GMP has been astonishing. Having overcome an initial disbelief, cyclic GMP has risen to its present eminence as a premium cellular signal transduction messenger of not only hormonal extracellular but also of the intracellular signals. This research topic focuses on the pathways and functions of membrane guanylate cyclases in different tissues of the body and their interplay with intracellular sensory signals where in many cases, cyclic GMP along with Ca2+ have taken on roles as synarchic co-messengers
    Note: English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Book
    Book
    New York :Raven Press,
    UID:
    almafu_BV001007348
    Format: XIV, 377 S. : Ill., graph. Darst.
    ISBN: 0-89004-244-6
    Series Statement: Progress in cancer research and therapy 9
    Language: English
    Subjects: Medicine
    RVK:
    Keywords: Hormonrezeptor ; Carcinogenese ; Hormon
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    UID:
    edocfu_9958106874002883
    Format: 1 online resource (185 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889195060
    Series Statement: Frontiers Research Topics
    Content: The development of the field of membrane guanylate cyclase transduction system has been colorful, filled with exceptional historical events in cellular signaling research. From denial to resurgence, the field has branched in multiple directions. The signal transduction characteristics and signaling elements are unique. The field has established cyclic GMP as an ubiquitous intracellular second messenger, playing a critical role in the control of many physiological processes, including cardiac vasculature, smooth muscle relaxation, blood volume, cellular growth, sensory transduction, neural plasticity, learning and memory. Unlike the three-component design of its predecessor: adenylate cyclase, G-protein and G-protein coupled receptor, the membrane guanylate cyclase transduction system consists of a single entity, a trans-membrane-spanning protein that serves as both a receptor and a signal transducer. Membrane guanylate cyclases exist in multiple forms. Each form translates the captured signal at a structurally conserved core catalytic site that resides in the intracellular domain. Yet the mechanism of capturing the signal is unique to each form. The surface receptor form uses its extracellular domain to capture hormonal signals; the Ca2+-modulated ROS-GC employs its intracellular domains; and the olfactory receptor ONE-GC captures odorant signals at its extracellular domain and amplifies them at multiple intracellular domains. The composition of the hormone receptor form differs from the ROS-GC and ONE-GC forms, consisting of a single polypeptide, that is both a signal receptor and the transducer. In contrast, both ROS-GC and ONE-GC are multi-component systems. A Ca2+ sensing subunit(s) captures the signal and transmits it to a companion guanylate cyclase, that transduces it. Moreover, the modes of signal transduction vary in ROS-GC and ONE-GC. ROS-GC is a direct transducer of Ca2+ signals but the Ca2+ sensors in ONE-GC only amplify the odorant signal received and transmitted by its extracellular domain. An additional refinement is that ROS-GC1 is a bimodal Ca2+ switch, turned “OFF” as intracellular [Ca2+] rises above 75 nM, but then turned back “ON” when [Ca2+] exceeds 345 nM. These modes occur uniquely in the outer segments and synapses of cones in rodent retinas. In a new paradigm change, the dogma has been shattered that the ANF hormone receptor guanylate cyclase, ANF-RGC, is the specific transducer of ANF alone. It is now known that ANF-RGC also transduces a Ca2+ signal. Ca2+ captured by its sensor neurocalcin δ (NCδ) directly activates the catalytic module of ANF-RGC. Accordingly, and impressively, targeted gene-deletion mouse model studies demonstrate that both pathways are linked with blood pressure regulation. Their disruption causes hypertension. Thus the ANF-RGC combines features of hormone receptor and ROS-GC forms of membrane guanylate cyclases. These studies also broaden the classification of the Ca2+ sensors. NCδ, classified as a neuronal calcium sensor, is more widespread. The general theme of this Research Topic is to present a comprehensive coverage of the expanding role being played by this beautifully designed transduction machinery. The reviews will cover its history to its present status, move on to theoretical and experimental investigations propelling the field in future directions, and provide illustrations where the field contributes to clinical medicine.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 5
    UID:
    edoccha_9958106874002883
    Format: 1 online resource (185 pages) : , illustrations; digital, PDF file(s).
    ISBN: 9782889195060
    Series Statement: Frontiers Research Topics
    Content: The development of the field of membrane guanylate cyclase transduction system has been colorful, filled with exceptional historical events in cellular signaling research. From denial to resurgence, the field has branched in multiple directions. The signal transduction characteristics and signaling elements are unique. The field has established cyclic GMP as an ubiquitous intracellular second messenger, playing a critical role in the control of many physiological processes, including cardiac vasculature, smooth muscle relaxation, blood volume, cellular growth, sensory transduction, neural plasticity, learning and memory. Unlike the three-component design of its predecessor: adenylate cyclase, G-protein and G-protein coupled receptor, the membrane guanylate cyclase transduction system consists of a single entity, a trans-membrane-spanning protein that serves as both a receptor and a signal transducer. Membrane guanylate cyclases exist in multiple forms. Each form translates the captured signal at a structurally conserved core catalytic site that resides in the intracellular domain. Yet the mechanism of capturing the signal is unique to each form. The surface receptor form uses its extracellular domain to capture hormonal signals; the Ca2+-modulated ROS-GC employs its intracellular domains; and the olfactory receptor ONE-GC captures odorant signals at its extracellular domain and amplifies them at multiple intracellular domains. The composition of the hormone receptor form differs from the ROS-GC and ONE-GC forms, consisting of a single polypeptide, that is both a signal receptor and the transducer. In contrast, both ROS-GC and ONE-GC are multi-component systems. A Ca2+ sensing subunit(s) captures the signal and transmits it to a companion guanylate cyclase, that transduces it. Moreover, the modes of signal transduction vary in ROS-GC and ONE-GC. ROS-GC is a direct transducer of Ca2+ signals but the Ca2+ sensors in ONE-GC only amplify the odorant signal received and transmitted by its extracellular domain. An additional refinement is that ROS-GC1 is a bimodal Ca2+ switch, turned “OFF” as intracellular [Ca2+] rises above 75 nM, but then turned back “ON” when [Ca2+] exceeds 345 nM. These modes occur uniquely in the outer segments and synapses of cones in rodent retinas. In a new paradigm change, the dogma has been shattered that the ANF hormone receptor guanylate cyclase, ANF-RGC, is the specific transducer of ANF alone. It is now known that ANF-RGC also transduces a Ca2+ signal. Ca2+ captured by its sensor neurocalcin δ (NCδ) directly activates the catalytic module of ANF-RGC. Accordingly, and impressively, targeted gene-deletion mouse model studies demonstrate that both pathways are linked with blood pressure regulation. Their disruption causes hypertension. Thus the ANF-RGC combines features of hormone receptor and ROS-GC forms of membrane guanylate cyclases. These studies also broaden the classification of the Ca2+ sensors. NCδ, classified as a neuronal calcium sensor, is more widespread. The general theme of this Research Topic is to present a comprehensive coverage of the expanding role being played by this beautifully designed transduction machinery. The reviews will cover its history to its present status, move on to theoretical and experimental investigations propelling the field in future directions, and provide illustrations where the field contributes to clinical medicine.
    Note: Bibliographic Level Mode of Issuance: Monograph , English
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 6
    Online Resource
    Online Resource
    Boston, MA : Springer
    UID:
    gbv_749183888
    Format: Online-Ressource (V, 190 p) , digital
    Edition: Springer eBook Collection. Biomedical and Life Sciences
    ISBN: 9781461509271
    Series Statement: Developments in Molecular and Cellular Biochemistry 36
    Content: From somewhat enigmatic beginnings 40 years ago, guanylate cyclase research has emerged to occupy a position of prominence in the study of signal transduction. Guanylate cyclase has several intriguing features, including existence in two major forms, membrane and soluble, each independently regulated by distinct mechanisms. The membrane form gives rise to a fascinating signal transduction story important to both peptide hormones and sensory neurons. This volume covers the evolution of the field, peptide hormone receptor work, membrane guanylate cycles, related retinal diseases, and the biochemistry and physiology of the soluble form. The 16 chapters are written by leaders in the field
    Additional Edition: ISBN 9781461353089
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 9781461353089
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 9780792376828
    Additional Edition: Erscheint auch als Druck-Ausgabe ISBN 9781461509288
    Language: English
    URL: Volltext  (lizenzpflichtig)
    Library Location Call Number Volume/Issue/Year Availability
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  • 7
    Book
    Book
    Dordrecht [u.a.] :Kluwer,
    UID:
    almahu_BV025276607
    Format: 188 S. : , Ill.
    ISBN: 0-7923-7682-X
    Series Statement: Developments in molecular and cellular biochemistry 36
    Note: Reprinted from: Molecular and cellular biochemistry ; 230(2002)
    Language: English
    Subjects: Biology
    RVK:
    RVK:
    Keywords: Guanylatcyclase ; Physiologische Chemie ; Guanylatcyclase ; Pathobiochemie ; Aufsatzsammlung
    Library Location Call Number Volume/Issue/Year Availability
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