| Title |
Programmed Cell Senescence during Mammalian Embryonic Development
|
|---|---|
| Published in |
Cell, November 2013
|
| DOI | 10.1016/j.cell.2013.10.019 |
| Pubmed ID | |
| Authors | |
| Abstract |
Cellular senescence disables proliferation in damaged cells, and it is relevant for cancer and aging. Here, we show that senescence occurs during mammalian embryonic development at multiple locations, including the mesonephros and the endolymphatic sac of the inner ear, which we have analyzed in detail. Mechanistically, senescence in both structures is strictly dependent on p21, but independent of DNA damage, p53, or other cell-cycle inhibitors, and it is regulated by the TGF-β/SMAD and PI3K/FOXO pathways. Developmentally programmed senescence is followed by macrophage infiltration, clearance of senescent cells, and tissue remodeling. Loss of senescence due to the absence of p21 is partially compensated by apoptosis but still results in detectable developmental abnormalities. Importantly, the mesonephros and endolymphatic sac of human embryos also show evidence of senescence. We conclude that the role of developmentally programmed senescence is to promote tissue remodeling and propose that this is the evolutionary origin of damage-induced senescence. |
Login to access the Attention Digest and the Sentiment Analysis related to this output.
X Demographics
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| United States | 6 | 18% |
| Spain | 3 | 9% |
| France | 1 | 3% |
| Netherlands | 1 | 3% |
| Peru | 1 | 3% |
| Egypt | 1 | 3% |
| United Kingdom | 1 | 3% |
| Switzerland | 1 | 3% |
| Unknown | 18 | 55% |
Demographic breakdown
| Type | Count | As % |
|---|---|---|
| Members of the public | 22 | 67% |
| Scientists | 7 | 21% |
| Science communicators (journalists, bloggers, editors) | 3 | 9% |
| Practitioners (doctors, other healthcare professionals) | 1 | 3% |
Mendeley demographics
Geographical breakdown
| Country | Count | As % |
|---|---|---|
| Spain | 7 | <1% |
| United States | 6 | <1% |
| United Kingdom | 6 | <1% |
| Japan | 4 | <1% |
| Germany | 3 | <1% |
| China | 3 | <1% |
| Netherlands | 2 | <1% |
| France | 2 | <1% |
| Trinidad and Tobago | 1 | <1% |
| Other | 7 | <1% |
| Unknown | 1493 | 97% |
Demographic breakdown
| Readers by professional status | Count | As % |
|---|---|---|
| Student > Ph. D. Student | 288 | 19% |
| Researcher | 225 | 15% |
| Student > Bachelor | 183 | 12% |
| Student > Master | 182 | 12% |
| Student > Doctoral Student | 63 | 4% |
| Other | 185 | 12% |
| Unknown | 408 | 27% |
| Readers by discipline | Count | As % |
|---|---|---|
| Biochemistry, Genetics and Molecular Biology | 467 | 30% |
| Agricultural and Biological Sciences | 352 | 23% |
| Medicine and Dentistry | 120 | 8% |
| Neuroscience | 43 | 3% |
| Immunology and Microbiology | 23 | 1% |
| Other | 93 | 6% |
| Unknown | 436 | 28% |