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Induction of telomerase in p21-positive cells counteracts capillaries rarefaction in aging mice lung

Authors :
Larissa Lipskaia
Marielle Breau
Christelle Cayrou
Dmitri Churikov
Laura Braud
Charles Fouillade
Sandra Curras-Alonso
Serge Bauwens
Frederic Jourquin
Frederic Fiore
Rémy Castellano
Emmanuelle Josselin
Carlota Sánchez-Ferrer
Giovanna Giovinazzo
Eric Gilson
Ignacio Flores
Arturo Londono-Vallejo
Serge Adnot
Vincent Géli
Centre de Recherche en Cancérologie de Marseille (CRCM)
Aix Marseille Université (AMU)-Institut Paoli-Calmettes
Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Fédération nationale des Centres de lutte contre le Cancer (FNCLCC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Publication Year :
2022
Publisher :
Cold Spring Harbor Laboratory, 2022.

Abstract

Telomerase is required for long-term cell proliferation and linked to stem cells. This is evident in the lung where short telomeres are associated with lung dysfunction. We constructed a mouse model in which the telomerase (Tert) is expressed from the p21Cdkn1apromoter. We found that this peculiar Tert expression curb age-related emphysema and pulmonary perivascular fibrosis in old mice. In old mice lungs, such Tert expression preferentially occurs in endothelial cells where it reduces the number of senescent endothelial cells. Remarkably, we report that Tert counteracts the age-related decline in capillary density. This was associated with an increased number of Cd34+ cells identified as a subclass of capillary cells with proliferative capacity. Expression of catalytically inactiveTertneither prevents the decline of capillary density in old mice nor protects against age-related emphysema and fibrosis. These findings reveal that telomerase decreases age-decline of pulmonary functions by sustaining microvasculature regeneration and outgrowth.

Details

Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....76acd2dc57bf0b2314dbb144a489e7c9
Full Text :
https://doi.org/10.1101/2022.10.27.514005