FKBP51 and FKBP52 in Signaling and Disease

Cheryl Samaniego

Research output: Contribution to journalArticlepeer-review

Abstract

FKBP51 and FKBP52 are diverse regulators of steroid hormone receptor signaling, including receptor maturation, hormone binding and nuclear translocation. Although structurally similar, they are functionally divergent, which is largely attributed to differences in the FK1 domain and the proline-rich loop. FKBP51 and FKBP52 have emerged as likely contributors to a variety of hormone-dependent diseases, including stress-related diseases, immune function, reproductive functions and a variety of cancers. In addition, recent studies have implicated FKBP51 and FKBP52 in Alzheimer's disease and other protein aggregation disorders. This review summarizes our current understanding of FKBP51 and FKBP52 interactions within the receptor-chaperone complex, their contributions to health and disease, and their potential as therapeutic targets for the treatment of these diseases.
Original languageAmerican English
Journal"Trends in Endocrinolgy and Metabolism "
Volume22
DOIs
StatePublished - Aug 31 2011

Keywords

  • Steroid Hormone Receptor Signaling
  • Receptor Maturation
  • Hormone Binding
  • Nuclear Translocation
  • Hormone Dependent Diseases
  • Stress Related Diseases

Disciplines

  • Biology
  • Cell Biology

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