An intercellular polyamine transfer via gap junctions regulates proliferation and response to stress in epithelial cells

Author:

Desforges Bénédicte1,Curmi Patrick A.1,Bounedjah Ouissame1,Nakib Samir2,Hamon Loic1,De Bandt Jean-Pascal23,Pastré David1

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale, UMR829, Laboratoire Structure-Activité des Biomolécules Normales et Pathologiques, Université Evry-Val d'Essonne, Evry 91025, France

2. Service de Biochimie, AP-HP Hôpitaux Universitaires Paris Centre, 75679 Paris, France

3. Laboratoire de Biologie de la Nutrition, EA4466, Département de Biologie Expérimentale, Métabolique et Clinique, Faculté de Pharmacie, Université Paris-Descartes, 75270 Paris, France

Abstract

In the organism, quiescent epithelial cells have the potential to resume cycling as a result of various stimuli, including wound healing or oxidative stress. Because quiescent cells have a low polyamine level, resuming their growth requires an increase of their intracellular polyamine levels via de novo polyamine synthesis or their uptake from plasma. Another alternative, explored here, is an intercellular exchange with polyamine-rich cycling cells via gap junctions. We show that polyamines promote gap junction communication between proliferating cells by promoting dynamical microtubule plus ends at the cell periphery and thus allow polyamine exchange between cells. In this way, cycling cells favor regrowth in adjacent cells deprived of polyamines. In addition, intercellular interactions mediated by polyamines can coordinate the translational response to oxidative stress through the formation of stress granules. Some putative in vivo consequences of polyamine-mediated intercellular interactions are also discussed regarding cancer invasiveness and tissue regeneration.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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