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Updated: Jul 1, 2026

Biochemical Reconstitution of Steroid Receptor•Hsp90 Protein Complexes and Reactivation of Ligand Binding
Published on: September 21, 2011
Rapid signaling by steroid receptors
1Department of Medicine, Veterans Affairs Medical Center, Long Beach, CA 90822, USA. ellis.levin@va.gov
Abstract:
Steroid receptors transcribe genes that lead to important biological processes, including normal organ development and function, tissue differentiation, and promotion of oncogenic transformation. These actions mainly result from nuclear steroid receptor action. However, for 50 years, it has been known that rapid effects of steroid hormones occur and could result from rapid signal transduction. Examples of these effects include stress responses to secreted glucocorticoids, rapid actions of thyroid hormones in the heart, and acute uterine/vaginal responses to injected estrogen. These types of responses have increasingly been attributed to rapid signaling by steroid hormones, upon engaging binding proteins most often at the cell surface of target organs. It is clear that rapid signal transduction serves an integrated role to modify existing proteins, altering their structure and activity, and to modulate gene transcription, often through collaboration with the nuclear pool of steroid receptors. The biological outcomes of steroid hormone actions thus reflect input from various cellular pools, cocoordinating the necessary events that are restrained in temporal and kinetic fashion. Here I describe the current understanding of rapid steroid signaling that is now appreciated to extend to virtually all members of this family of hormones and their receptors.
Insights
Rapid steroid signaling, initiated at the cell surface, complements nuclear receptor actions. This pathway rapidly modifies proteins and influences gene transcription for diverse biological outcomes.
Area of Science:
- Endocrinology
- Molecular Biology
- Cellular Signaling
Background:
- Steroid receptors primarily mediate gene transcription via nuclear actions, influencing development and disease.
- Rapid, non-genomic effects of steroid hormones have been observed for decades, suggesting alternative signaling pathways.
Purpose of the Study:
- To review the current understanding of rapid steroid signaling pathways.
- To highlight the integrated role of rapid signaling with nuclear receptor actions.
Main Methods:
- Literature review of studies on rapid steroid hormone effects.
- Analysis of signaling mechanisms involving cell surface receptors and protein modification.
- Integration of rapid signaling with nuclear transcription modulation.
Main Results:
- Rapid steroid signaling is initiated at the cell surface, engaging specific binding proteins.
- This signaling pathway rapidly alters protein structure and activity.
- Rapid signaling collaborates with nuclear steroid receptors to modulate gene transcription.
Conclusions:
- Rapid steroid signaling is a widespread phenomenon, extending to most steroid hormone-receptor systems.
- These rapid actions are crucial for coordinating biological responses with nuclear actions.
- Understanding both rapid and nuclear signaling provides a comprehensive view of steroid hormone function.
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