AGING: Small heat shock proteins prevent harmful aggregations.

From: Brett Paatsch (paatschb@optusnet.com.au)
Date: Thu May 15 2003 - 22:31:02 MDT

  • Next message: Spudboy100@aol.com: "Re: [Liberal Bias] Leftist Spin on Twisters"

    Researchers discover common cause for aging and age-related disease

    http://www.eurekalert.org/pub_releases/2003-05/uoc--rdc051303.php

    "Why do serious diseases such as cancer, Alzheimer's and Huntington's mainly
    hit us in middle age or later? The links between aging and age-related
    diseases have proved elusive.

    In studies of the powerfully informative roundworm, C. elegans, UCSF
    scientists have discovered that a class of molecules found in the worms and
    in people can both prolong life in the worm and prevent the harmful
    accumulation of abnormal proteins that cause a debilitating
    Huntington's-like disease. The finding appears to be the first evidence in
    an animal of a link between aging and age-related disease.

    The molecules, called "small heat-shock proteins," are known to assemble
    into complexes that bind to damaged or unfolded cellular proteins and
    prevent them from forming into harmful aggregations. "

    etc..

    .......

    Or the actual 16 May Science article refered from the above...
    http://www.sciencemag.org/cgi/content/abstract/300/5622/1142

    Regulation of Aging and Age-Related Disease by DAF-16 and Heat-Shock Factor
    Ao-Lin Hsu, Coleen T. Murphy, Cynthia Kenyon*

    The Caenorhabditis elegans transcription factor HSF-1, which regulates the
    heat-shock response, also influences aging. Reducing hsf-1 activity
    accelerates tissue aging and shortens life-span, and we show that hsf-1
    overexpression extends lifespan. We find that HSF-1, like the transcription
    factor DAF-16, is required for daf-2-insulin/IGF-1 receptor mutations to
    extend life-span. Our findings suggest this is because HSF-1 and DAF-16
    together activate expression of specific genes, including genes encoding
    small heat-shock proteins, which in turn promote longevity. The small
    heat-shock proteins also delay the onset of polyglutamine-expansion protein
    aggregation, suggesting that these proteins couple the normal aging process
    to this type of age-related disease.

    ----
    Brett Paatsch
    


    This archive was generated by hypermail 2.1.5 : Thu May 15 2003 - 22:41:48 MDT