TY - JOUR
T1 - Insulin/IGF-1 and ROS signaling pathway cross-talk in aging and longevity determination
AU - Papaconstantinou, John
N1 - Funding Information:
This publication was supported by USPHS grant 1P01 AG021832-04 awarded by the National Institute on Aging, and the USPHS grant 1 P30 AG024832-03, the Claude D. Pepper Older Americans Independence Center grant awarded by the National Institute on Aging, and by the UTMB Sealy Center on Aging.
PY - 2009/2/5
Y1 - 2009/2/5
N2 - Regulation of hormonal, insulin/IGF-1 (Ins/IGF-1) signaling activities, and pathways of the intrinsic generation of reactive oxygen species (ROS) play a role in aging and longevity determination. In this review we discuss the cross-talk between these pathways as mechanisms of signaling that may be important factors in the regulation of aging and longevity. The balance of physiological processes controlling the rate of aging and longevity in several mouse mutants suggests the involvement of cross-talk mechanisms of regulation of the insulin/IGF1 signaling pathway vs. the ROS signaling pathways. In mice, modulation of the Ins/IGF-1 signaling pathways resulting from the Prop1df, Pit1dw and Igf1 receptor mutations exemplify the hormonal pathways associated with aging and longevity determination. These pathways are also targets of the ROS-mediated redox pathways. Similarly, the Klotho and p66Shc mutants link regulation of ROS signaling pathways to aging and longevity determination. Both of these models also display altered insulin signaling activity, a characteristic associated with longevity. The Ins/IGF-1 signaling pathway is of particular interest because of its decreased activity due to genetic manipulation vs. its responsiveness to ROS levels.
AB - Regulation of hormonal, insulin/IGF-1 (Ins/IGF-1) signaling activities, and pathways of the intrinsic generation of reactive oxygen species (ROS) play a role in aging and longevity determination. In this review we discuss the cross-talk between these pathways as mechanisms of signaling that may be important factors in the regulation of aging and longevity. The balance of physiological processes controlling the rate of aging and longevity in several mouse mutants suggests the involvement of cross-talk mechanisms of regulation of the insulin/IGF1 signaling pathway vs. the ROS signaling pathways. In mice, modulation of the Ins/IGF-1 signaling pathways resulting from the Prop1df, Pit1dw and Igf1 receptor mutations exemplify the hormonal pathways associated with aging and longevity determination. These pathways are also targets of the ROS-mediated redox pathways. Similarly, the Klotho and p66Shc mutants link regulation of ROS signaling pathways to aging and longevity determination. Both of these models also display altered insulin signaling activity, a characteristic associated with longevity. The Ins/IGF-1 signaling pathway is of particular interest because of its decreased activity due to genetic manipulation vs. its responsiveness to ROS levels.
KW - Aging
KW - Insulin/IGF-1 signaling
KW - Longevity
KW - ROS signaling
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U2 - 10.1016/j.mce.2008.11.025
DO - 10.1016/j.mce.2008.11.025
M3 - Review article
C2 - 19103250
AN - SCOPUS:58349097705
SN - 0303-7207
VL - 299
SP - 89
EP - 100
JO - Molecular and Cellular Endocrinology
JF - Molecular and Cellular Endocrinology
IS - 1
ER -