A growing number of proteins devoid of signal peptides have been demonstrated to be released through the non-classical pathways independent of endoplasmic reticulum and Golgi. Among them are two potent proangiogenic cytokines FGF1 and IL1α. Stress-induced transmembrane translocation of these proteins requires the assembly of copper-dependent multiprotein release complexes. It involves the interaction of exported proteins with the acidic phospholipids of the inner leaflet of the cell membrane and membrane destabilization. Not only stress, but also thrombin treatment and inhibition of Notch signaling stimulate the export of FGF1. Non-classical release of FGF1 and IL1-α presents a promising target for treatment of cardiovascular, oncologic, and inflammatory disorders.

Secretion without Golgi / I. PRUDOVSKY; F. TARANTINI; M. LANDRISCINA; D. NEIVANDT; R. SOLDI; A. KIROV; D. SMALL; KM. KATHIR; D. RAJALINGAM; TK. KUMAR. - In: JOURNAL OF CELLULAR BIOCHEMISTRY. - ISSN 0730-2312. - STAMPA. - 103:(2008), pp. 1327-1343.

Secretion without Golgi.

TARANTINI, FRANCESCA;
2008

Abstract

A growing number of proteins devoid of signal peptides have been demonstrated to be released through the non-classical pathways independent of endoplasmic reticulum and Golgi. Among them are two potent proangiogenic cytokines FGF1 and IL1α. Stress-induced transmembrane translocation of these proteins requires the assembly of copper-dependent multiprotein release complexes. It involves the interaction of exported proteins with the acidic phospholipids of the inner leaflet of the cell membrane and membrane destabilization. Not only stress, but also thrombin treatment and inhibition of Notch signaling stimulate the export of FGF1. Non-classical release of FGF1 and IL1-α presents a promising target for treatment of cardiovascular, oncologic, and inflammatory disorders.
2008
103
1327
1343
I. PRUDOVSKY; F. TARANTINI; M. LANDRISCINA; D. NEIVANDT; R. SOLDI; A. KIROV; D. SMALL; KM. KATHIR; D. RAJALINGAM; TK. KUMAR
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/256868
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