Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2004 Jun 1;199(3):127-34.
doi: 10.1007/s00232-004-0685-8.

Nuclear envelope: nanoarray responsive to aldosterone

Affiliations
Review

Nuclear envelope: nanoarray responsive to aldosterone

H Oberleithner. J Membr Biol. .

Abstract

Signalling between cytosol and nucleus is mediated by nuclear pores. These supramolecular complexes represent intelligent nanomachines regulated by a wide spectrum of factors. Among them, steroid hormones specifically interact with the pores and thus modify ion conductivity and macromolecule permeability of the nuclear envelope. In response to aldosterone the pores undergo dramatic changes in conformation, changes that depend on the nature of the transported cargo. Such changes can be imaged at the nanometer scale by using atomic force microscopy. Furthermore, steroid-induced macromolecule transport across the nuclear envelope causes osmotic water movements and nuclear swelling. Drugs that interact with intracellular steroid receptors (spironolactone) or with plasma membrane sodium channels (amiloride) inhibit swelling. Steroid hormone action is blocked when nuclear volume changes are prevented. This is shown in frog oocytes and human endothelial cells. In conclusion, nuclear pores serve as steroid-sensitive gates that determine nuclear activity.

PubMed Disclaimer

Similar articles

References

    1. Proc Natl Acad Sci U S A. 2002 May 14;99(10):7154-9 - PubMed
    1. J Biol Chem. 1998 Feb 27;273(9):4883-91 - PubMed
    1. Proc Natl Acad Sci U S A. 1996 Aug 6;93(16):8756-60 - PubMed
    1. Kidney Int. 2000 Apr;57(4):1390-4 - PubMed
    1. Cell Physiol Biochem. 2000;10(5-6):429-34 - PubMed

Publication types

MeSH terms

LinkOut - more resources