Reverse Aging Cocktail
Scientists have created a cocktail of drugs that reverses signs of cell aging in cells. Their team utilized rapamycin and trametinib, two widely prescribed medicines used for organ rejection prevention.
Both drugs have also been demonstrated to extend animal lifespans in multiple studies. Of the six chemical combinations studied, all six showed statistically improved compartmentalization within senescent cells while simultaneously decreasing their estimated transcriptomic age without altering cell identity or altering compartmentalization within them.
Cellular Rejuvenation
Cellular rejuvenation is a treatment designed to make cells healthier, which in turn improves skin health, energy levels and overall well-being. Cellular rejuvenation utilizes stem cells and exosomes to regenerate your body into looking younger with renewed vitality. While many assume cellular rejuvenation treatments are solely intended for older individuals, anyone can benefit from rejuvenating their cells; some treatments may even produce long-lasting benefits that continue providing benefits even years later!
Research into aging has unlocked key mechanisms that underlie both aging and age-related disease, providing us with an opportunity to develop therapies to halt or reverse aging and extend healthy lifespans. But translating these discoveries into clinically available therapies requires scientific rigor as well as multidisciplinary collaboration to achieve broad application and accessibility.
Epigenetic reprogramming has emerged as a promising approach for rejuvenation of cells. It involves reactivating genes that have been silenced due to environmental influences or effects of aging such as telomere attrition, genomic instability, deregulated nutrient sensing, loss of proteostasis, mitochondrial dysfunction or reduced intercellular communication.
Rejuvenation strategies have been found to extend lifespans and slow or reverse age-related diseases, yet their fundamental principles remain mostly unknown and costly methods limited therapeutic applications.
Rejuvenation therapies remain some way from mainstream clinical application, yet there remains reason for optimism. Customized approaches such as genetic and phenotypic profiling could enable clinicians to tailor treatment strategies according to patient characteristics. This would reduce costs, improve patient compliance and decrease risks associated with gene editing or cell reprogramming techniques. Development of blood-based biomarkers of senescent cell clearance or rejuvenation proteins could streamline clinical trials and enhance patient monitoring, making cellular rejuvenation therapies more accessible and clinically viable, ushering in a new era of healthcare that prioritizes health preservation and longevity.
Transcriptomic Clock Analysis
Current research into cellular rejuvenation aims to understand and identify the specific mechanisms by which interventions may influence aging, with an aging clock as one key tool to assist this effort. Aging clocks use various measurements such as cell proliferation, senescence and chromatin modification states to predict chronological age – however most have platform or tissue-specific limitations and limited accessibility which impede their usefulness.
Recently, deep learning methods have been employed to create computational models using various measured data sets such as genomic, protein expression and metabolic measurements to accurately predict chronological age. These models are known as spatial aging clocks, and have shown outstanding performance both bulk and single cell RNA-seq experiments.
Performance of a spatial aging clock depends on its ability to identify local patterns of age acceleration and predict relative chronological ages of cells within brain sections. Performance can also be enhanced by training the clock on multiple brain sections from independent mice, which allows it to determine which factors influence ageing in specific regions and generalize predictions across experimental conditions and brain regions.
We employed spatial ageing clocks on coronal brain sections from rats and mice, and found that cell ages in a given region correlated with distance to sites of demyelination injury. These results demonstrate how regional approaches may be more useful when measuring effects of interventions; spatial aging clocks provide one such powerful tool.
Furthermore, we demonstrated the reproducibility and generalization of spatial ageing clocks by comparing their predicted ages with those measured via immunofluorescence on isolated T cells and NSCs from various mice and sections. Furthermore, their predictive power remained independent from any definition of proximity effect (Supplementary Fig. 6a and b).
As well, both neural and RNAageCalc clocks demonstrated strong rejuvenating effects on endothelial cells, pericytes, and vascular smooth muscle cells – similar to exercise’s widespread benefits – consistent with widespread exercise effects. Furthermore, we discovered that both clocks were associated with strong rejuvenating effects on endothelial cells, pericytes, and vascular smooth muscle cells, suggesting widespread exercise benefits. RNAageCalc clock was associated with both psychiatric disorders in our samples while neural clock was only associated with opioid misuse as well as orbitofrontal and subgenual prefrontal cortex activity (sgPFC activity).
Transcriptomic Profiling of Senescent Cells
Senescent cells accumulate with age in organs and contribute to various diseases through the release of pro-survival and inflammatory factors. To understand how senescent cells contribute to aging, it is crucial to analyze their genome-wide transcriptomes. Senescent cells exhibit a distinct transcriptional profile characterized by classical senescence markers such as p53 and p21 expression – this signature can vary depending on both its cause as well as when induction takes place.
Our systematic transcriptomic analysis identifies distinct senescent populations that differ significantly from each other and the non-senescent population. A subset of cells called Cluster 6 express high levels of ECM proteases and antiapoptotic proteins mRNA, while having low expression of oxidative phosphorylation proteins and SASP factors; furthermore they display elevated expression of long noncoding RNAs such as LncRNAs. Cluster 6 cells could be found across all senescence models; making up over 50% of both populations; they displayed elevated p53 and p21 levels, suggesting active DNA damage signalling activity.
OSK significantly reversed expression of genes related to senescence, leading to decreased cell death associated with this process. Yet, further DNA damage may still be required to maintain cell cycle arrest – possibly caused by either SASP-driven inflammation response or unresolved damage caused by initial stimulation that led to inducing senescence induction stimulus.
Additionally, our genome-wide transcriptomic analyses identify numerous transcriptional regulators influenced by different models of senescence induction, such as upregulating chromatin remodeling gene p53 when exposed to OSK treatment and reduced expression of CASP3, JAK-STAT and NFkB genes involved in cell senescence pathway genes like CASP3, JAK-STAT and NFkB which suggest these pathways might play an essential role in countering the negative impacts associated with aging-related phenotypes.
Transcriptional landscape of senescent cells depends on tissue context and cell identity, yet our results demonstrate that reverse senescence with OSK can restore a youthful genome-wide transcriptome in less than a week without impacting cellular identity. These results demonstrate how rejuvenating senescent fibroblasts with chemical intervention is possible while supporting epigenetic reprogramming as an epigenetic method to reverse senescence.
Conclusions
Researchers have developed a chemical cocktail they claim can halt mouse aging within seven days by rejuvenating cells inside muscles, tissues, and some organs. It contains anti-inflammatory drug rapamycin as well as three other medications known to extend lifespan like antiseizure medication Valproic Acid, CHIR-99021, and Tranylcypromine which have all proven themselves effective against mouse aging.
To test whether these chemicals could actually reverse aging, the team employed high-throughput cell-based assays and transcription-based aging clocks that distinguished between young and aged connective tissue cells (fibroblasts). Researchers employed a technique measuring nucleocytoplasmic compartmentalization to identify small molecules which help rejuvenate senescent cells back into stem cell state, rejuvenating them back to stem cell-like status. They evaluated 80 cocktail samples with this approach and identified six that statistically improved compartmentalization in senescent cells. Furthermore, gene activity profiles were measured to verify that these treatments actually reversed aging; all eight cocktails decreased biological and chronological aging below that seen even in nonsenescent cells.
The team tested its cocktails in vivo on mice by giving them injections, before subjecting them to various tests of muscle endurance and strength. Their team discovered that these cocktails reduced fat mass in mice as well as improving their ability to grip rotating rods with longer times on it indicating increased endurance. Furthermore, this cocktail enhanced learning and memory as well as reduced age-related heart, lung, kidney and liver lesions in these animals.
These findings are promising, yet there remains much work to do before this anti-aging cocktail can be approved for human use. First, the cocktail must undergo rigorous tests to ensure no adverse side effects such as cancer or other serious conditions occur as a result of taking it. Second, this therapy must be combined with therapies which address cellular-level processes associated with aging. Targeting multiple biological pathways at once will likely prove more successful than any single approach to improving cell function, according to researchers’ work, with hopes that its findings inspire future studies of human reprogramming strategies.
