The reticulons: Guardians of the structure and function of the endoplasmic reticulum
- 1. Department of Biology, University of Rome "Tor Vergata", Via della Ricerca Scientifica 1, 00133 Rome (Italy)
- 2. National Institute for Infectious Diseases, IRCCS "L. Spallanzani", Via Portuense, 00149 Rome (Italy)
Description
The endoplasmic reticulum (ER) consists of the nuclear envelope and a peripheral network of tubules and membrane sheets. The tubules are shaped by a specific class of curvature stabilizing proteins, the reticulons and DP1; however it is still unclear how the sheets are assembled. The ER is the cellular compartment responsible for secretory and membrane protein synthesis. The reducing conditions of ER lead to the intra/inter-chain formation of new disulphide bonds into polypeptides during protein folding assessed by enzymatic or spontaneous reactions. Moreover, ER represents the main intracellular calcium storage site and it plays an important role in calcium signaling that impacts many cellular processes. Accordingly, the maintenance of ER function represents an essential condition for the cell, and ER morphology constitutes an important prerogative of it. Furthermore, it is well known that ER undergoes prominent shape transitions during events such as cell division and differentiation. Thus, maintaining the correct ER structure is an essential feature for cellular physiology. Now, it is known that proper ER-associated proteins play a fundamental role in ER tubules formation. Among these ER-shaping proteins are the reticulons (RTN), which are acquiring a relevant position. In fact, beyond the structural role of reticulons, in very recent years new and deeper functional implications of these proteins are emerging in relation to their involvement in several cellular processes.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.yexcr.2012.03.002Additional details
Identifiers
- DOI
- 10.1016/j.yexcr.2012.03.002;
- PII
- S0014-4827(12)00129-2;
Publishing Information
- Journal Title
- Experimental Cell Research
- Journal Volume
- 318
- Journal Issue
- 11
- Journal Page Range
- p. 1201-1207
- ISSN
- 0014-4827
- CODEN
- ECREAL
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45033224
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- APOPTOSIS; CELL DIVISION; ENDOPLASMIC RETICULUM; MEMBRANE PROTEINS; MORPHOLOGY; PHYSIOLOGY; POLYPEPTIDES
- Descriptors DEC
- CELL CONSTITUENTS; ORGANIC COMPOUNDS; PEPTIDES; PROTEINS
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.