Journal
OPEN BIOLOGY
Volume 10, Issue 12, Pages -Publisher
ROYAL SOC
DOI: 10.1098/rsob.200309
Keywords
senescence-associated secretory phenotype; macrophage; regeneration; senescence; ageing; repair
Categories
Funding
- Wellcome Trust [108906/Z/15/Z]
- UKRI/MRC [MR/S005544/1]
- MRC [MR/R015635/1, MR/S005544/1] Funding Source: UKRI
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Over the last decade, our understanding of the physiological role of senescent cells has drastically evolved, from merely indicators of cellular stress and ageing to having a central role in regeneration and repair. Increasingly, studies have identified senescent cells and the senescence-associated secretory phenotype (SASP) as being critical in the regenerative process following injury; however, the timing and context at which the senescence programme is activated can lead to distinct outcomes. For example, a transient induction of senescent cells followed by rapid clearance at the early stages following injury promotes repair, while the long-term accumulation of senescent cells impairs tissue function and can lead to organ failure. A key role of the SASP is the recruitment of immune cells to the site of injury and the subsequent elimination of senescent cells. Among these cell types are macrophages, which have well-documented regulatory roles in all stages of regeneration and repair. However, while the role of senescent cells and macrophages in this process is starting to be explored, the specific interactions between these cell types and how these are important in the different stages of injury/reparative response still require further investigation. In this review, we consider the current literature regarding the interaction of these cell types, how their cooperation is important for regeneration and repair, and what questions remain to be answered to advance the field.
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