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NYC Bone Seminar on Tuesday,November 16th: Janet Rubin,Professor of Medicine at Emory will speak on "Turning MechanicalSignals into Biological Effects."

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  • NYC Bone Seminar on Tuesday,November 16th: Janet Rubin,Professor of Medicine at Emory will speak on "Turning MechanicalSignals into Biological Effects."

    Dear colleagues and students:

    The third seminar in the Fall 2004 Bone Seminar Series will be on
    Tuesday November 16th with a presentation by Janet Rubin, Professor
    of Medicine in the Division of Endocrinology and Metabolism at the
    Emory School of Medicine. Janet will speak on "Turning Mechanical
    Signals into Biological Effects."

    Details of all seminars appear on our website: http://bonenet.net/index.html
    Details of this seminar appear below.

    I would greatly appreciate in any person interested in the Bone
    Seminar Series, the Bone Fluid Flow Workshops or the BoneNet.net
    website http://bonenet.net, filling out a questionnaire to help me
    prepare the annual report to the National Science Foundation, which
    supports these activities. The questionnaire is also downloadable at
    http://bonenet.net/questionnaire_0409.pdf.

    Many thanks, Steve Cowin

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    Speaker: Janet Rubin M.D., Professor of Medicine, Division of
    Endocrinology and Metabolism, Emory University School of Medicine and
    the Atlanta Veterans Affairs Medical Center, Atlanta, GA

    Title: TURNING MECHANICAL SIGNALS INTO BIOLOGICAL EFFECTS

    PLACE AND TIME: Room 9207, CUNY Graduate Center
    7:00 PM, November 16th, 2004

    Abstract: Biophysical input generated during normal physiologic
    loading is a major determinant of bone mass and morphology. Our
    laboratory's interest is in how bone cells sense and transduce
    signals generated during loading, and how this cellular response
    leads to skeletal adaptation to its mechanical environment. We have
    shown that substrate strain regulates gene expression in bone stromal
    cells, decreasing expression of RANKL and increasing expression of
    eNOS/nitric oxide. These changes generate a local environment that
    is inhibitory for osteoclast recruitment. The ability of mechanical
    strain to induce this functional response requires activation of the
    ERK1/2 MAP-Kinase pathway. The proximal signaling cascade leading to
    ERK1/2 activation is stunningly specific, and suggests that the
    putative mechanotransducer occupies a discrete membrane location.
    Our most recent work suggests that the mechanical signal arises from
    events occurring within a lipid raft. Distal to ERK1/2 activation,
    we will also consider possible mechanisms by which strain may inhibit
    RANKL gene transcription through altering chromatin interactions with
    the RANKL promoter. By defining the mechanisms involved in strain
    regulation of osteoclast formation we hope to generate new paradigms
    for understanding how cells convert mechanical information into
    biological effects.

    RESEARCH INTERESTS OF Janet Rubin: Mechanical and hormonal control
    of bone remodeling, gene therapy systems, tumor metastases in bone

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    Questions and Feedback Contact

    Stephen C. Cowin PhD
    New York Center for Biomedical Engineering
    Departments of Biomedical and Mechanical Engineering
    School of Engineering
    The City College of New York
    138th Street and Convent Avenue
    New York, NY 10031-9198, USA

    Phone:
    (212) 799-7970 (Office at Home)
    (212) 650-5208 (Office at Work)

    Fax:
    (212) 799-7970 (Office at Home)

    Email:
    scowin@earthlink.net

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