- Two studies published in Cell describe senescence as a normal and critical process during embryogenesis. They attribute a completely new and unexpected role to this process, which was always linked to aging and cancer.
- Researchers at the Centre for Genomic Regulation (CRG) in Barcelona share these findings with researchers at the Centro Nacional de Investigaciones Oncológicas (CNIO) in Madrid, publishing two back-to-back papers in the journal Cell.
“For the first time, these studies clearly show that senescence is a programmed developmental mechanism. This new description helps us to understand the role and significance of senescence as a normal cellular process”, explains Bill Keyes, head of the Mechanisms of Cancer and Aging laboratory at the CRG. “Our work demonstrates that in the embryo, the senescent cells are required, and through their normal secretory function, instruct tissue growth and patterning”, adds Dr. Keyes.
Keyes and collaborators describe senescence as a fundamental part of the biology of two major signalling centres in the embryo that helps to control normal limb and nervous system development. Likewise, the CNIO study led by Manuel Serrano, and postdoctoral researcher Daniel Munoz-Espin, identified identical processes in two other tissues, in the developing kidneys and ear.
Both studies then go on to show how the coordinated removal of senescent cells by macrophages plays a key role in the remodelling of the developing tissues, a process that is required for normal patterning. Interestingly, the tissues where the researchers describe the occurrence of senescence are among those most frequently affected by congenital birth defects, suggesting that an investigation of the mechanisms that regulate senescence in the embryo might help to explain the causes of some developmental abnormalities.
Thanks to this new perspective of senescence, the scientists suggest that senescence related to aging and cancer is an evolutionary adaptation of a developmental mechanism. “Hopefully, with the identification of senescence in a normal setting in the embryo, this will allow us to identify new mediators and biomarkers of senescence in future studies” says Mekayla Storer, a PhD student in the CRG and first author on the study, adding that “these findings change the way we understood senescence in the past, and give us novel important information to tackle cancer and aging”.
The work performed by the researchers at the CRG was funded by the Spanish Ministry for Science and Education, the Centre for Genomic Regulation, and studentships from “La Caixa”.
- Senescence is a developmental mechanism that contributes to embryonic growth patterning. Mekayla A Storer, Alba Mas, Alexandre Robert-Moreno, Matteo Pecoraro, M Carmen Ortells, Valeria Di Giacomo, Reut Yosef, Noam Pilpel, Valery Krizhanovsky, James Sharpe, Bill Keyes. Cell (2013). DOI: http://dx.doi.org/10.1016/j.cell.2013.10.041
- Programmed cell senescence during mammalian embryonic development. Daniel Muños-Espín, Marta Cañamero, Antonio Maraver, Gonzalo Gómez-López, Julio Contreras, Silvia Murillo-Cuesta, Alfonso Rodríguez-Baeza, Isabel Varela-Nieto, Jesús Ruberte, Manuel Collado, Manuel Serrano. Cell (2013). DOI: http://dx.doi.org/10.1016/j.cell.2013.10.019
Laia Cendrós, Press Officer – Centre for Genomic Regulation (CRG) – Phone: +34 93 316 0237.