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How to Renew Your Own Stem Cells

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How to Renew Your Own Stem Cells
8 months ago 4753 Views

Our message back then was that therapeutic cloning of stem cells might enable our biology to be transported back in time to a younger state.

In that 2002 magazine article, we described how fresh, young stem cells can regenerate tissues throughout our body, thereby reversing the course of degenerative disorders. Stem cell research, however, was torpedoed by federal edict in 2001 and has only recently regained serious momentum. The encouraging news is that we may be able to regenerate our existing pool of stem cells today. The significance of this cannot be overstated. If we replenish our pool of healthy stem cells, we may regain the ability to repopulate our tissues with fresh functional cells. The good news is that certain nutrients that readers of this magazine already supplement with have stem cell-renewing properties. This can buy precious time as ongoing research develops systemic stem cell rejuvenation therapies envisioned 20 years ago.

Stem Cells Needed to Sustain Life

Our tissues rely on functional cells to sustain organ viability. With age, our functional cells deteriorate. In youth, as functional cells die off, they are replaced with new cells created from stem cells present in our body.1-3

Stem cells, however, are affected by the same degenerative problems as functional cells.4 As stem cell vitality deteriorates, we lose the ability to repopulate tissues with fresh functional cells.4 What few people understand is that stem cells are capable of self-renewal, as well as producing mature functional cells.1,4

In medical practice today, stem cells are used for regenerative purposes. This is evidenced by the ability of bone marrow stem cell transplants to help leukemia patients.5 Based on the phenomenon of self-renewal, if our old stem cells can be reactivated, the effect could be whole-body rejuvenation. Nutritional interventions may provide an effective approach to activate dormant stem cells, thereby enhancing tissue regeneration. Using several lines of preclinical evidence from the scientific literature, we can outline a rational approach that could allow us to reactivate aging stem cells.

Stem Cells Are Retained with Age

Many stem cells are retained as we age and have the capacity to self-renew and differentiate into mature functional cells.4 Several factors that drive the aging process also reduce the regenerative potential of stem cells and contribute to worsening of age-related conditions.4 We now have a better understanding of specific degenerative pathways of aged tissues and how this contributes to disease, decline, and death.4,6 This gives us targets for restoring stem cell function and self-renewal using current technologies.4,6

Rejuvenating Aged Stem Cells

Normal aging (along with excess calorie ingestion) causes AMPK and NAD+ to plummet, mTOR to be imbalanced, and SIRT1 signaling to be downregulated.7-10

The impact of this is depletion of our stem cell pools and a reduced regenerative potential.11 Stem cell malfunction can be partially corrected with many of the nutrients that readers of Life Extension® magazine supplement with today. This includes curcumin,12,13 resveratrol,14-16 Gynostemma pentaphyllum,17 NAD+ precursors,18,19 along with sensible eating patterns.23

Stem Cell Rejuvenation in Laboratory Models

The challenge of maintaining healthy stem cells requires fighting off the same damaging factors that compromise our functional tissue cells. These factors include damaged DNA, mitochondrial dysfunction, chronic inflammation, and oxidative stress.

Emerging data indicate that interventions that blunt the effects of excessive calorie intake can rejuvenate some lineages of stem cells by:11,23-25

  • Activating AMPK
  • Suppressing mTOR
  • Boosting sirtuins

Sirtuins are indispensable for DNA repair, controlling inflammation and other life-sustaining processes. Resveratrol activates sirtuins but requires NAD+ for optimal functionality.26 In aged mice, treatment with the NAD+ precursor nicotinamide riboside rejuvenated muscle stem cells.19 This study showed that boosting NAD+ improved mitochondrial function in muscle stem cells and inhibited stem cell senescence. The researchers also showed that boosting NAD+ decreased senescence of brain and skin stem cells.19 An ongoing clinical trial may reveal neurological improvement in response to aggressive NAD+ boosting therapy.27 Clinical trials have demonstrated that oral administration of NAD+ precursors results in increased NAD+ levels,28,29 which are vital for stem cell functionality.19

AMPK + Resveratrol + NAD+ = Stem Cell Rejuvenation

In response to resveratrol, cells express proteins called sirtuins that provide several benefits including generating new mitochondria.30

Sirtuins are dependent on NAD+ to interact with FoxO, a beneficial transcription factor, to promote healthy gene expression.26,31 The cellular enzyme AMPK has a dynamic interaction with sirtuin 1 (SIRT1). The potential combined benefit of boosting AMPK, NAD+, SIRT1 and FoxO is the favorable impact this might have in promoting stem cell health. Moreover, AMPK activity helps to normalize excess mTOR, which can impede stem cell functionality.23

MULTI-MODAL APPROACH TO STEM CELL RENEWAL

We now know of several factors involved in the maintenance and potential rejuvenation of our aging stem cells.

The encouraging aspect of all this is we can target these stem cell renewal processes today via:

  1. AMPK activation35
  2. Sirtuin activation24,54
  3. FoxO activation55,56
  4. NAD+ replenishment19
  5. mTOR regulation (via AMPK activation)6,57

This approach may enable elderly individuals to rejuvenate their aged stem cells, which would then repopulate senile tissues with fresh, functional (somatic) cells.

Understanding the Role of mTOR in Obesity and Aging

“mTOR” stands for the mechan-istic target of rapamycin.

It is a protein found inside most cells and is responsible for regulating cellular growth by sensing and integrating diverse nutritional and environmental cues.7 Excessive activation of cellular mTOR is involved in diseases plaguing aging populations, such as cancer, type II diabetes, and obesity.7 Regulating mTOR activity extends lifespan in laboratory models by delaying the development of chronic diseases, including cancer.32 Maintenance of stem cell pools requires a finely tuned balance between stem cell renewal and differentiation.6

When mTOR is excessively activated in certain stem cell lineages, the pool of stem cells becomes exhausted.32 This diminishes our ability to regenerate our tissues with fresh functional cells.6 When properly balanced, mTOR will not adversely impact cellular aging.33-37 Enhancing autophagy in hemato-poietic stem cells improves their regenerative capacity.38 One way of inducing autophagy is suppression of excess mTOR via AMPK activation.38

According to a report published in the journal Nature:

“…it will be exciting to test whether rejuvenation interventions aimed at activating autophagy in unhealthy autophagy-inactivated oHSCs [old hematopoietic stem cells] will improve the health of the aging blood system.”38

Most People Need to Lower mTOR

The regulation of mTOR represents a viable approach to preserve the stem cell pool. This, in turn, would help maintain the functionality of our tissues and organs over time.

When calorie intake is reduced, mTOR activity diminishes, and autophagy is beneficially activated. This process (autophagy) cleans up accumulated cellular waste products and preserves cell function.39 The autophagy-regulating signaling network that includes AMPK and mTOR serves to maintain this delicate autophagy balance.40 Interventions that activate AMPK serve to balance mTOR and enable optimal levels of cellular autophagy.

Boost Cell AMPK To Lower mTOR

AMPK was first identified in 1973 for its role in fat metabolism.41 Based on evidence from preclinical studies, it is expected that when people practice severe calorie restriction, AMPK activity increases, which confers protective effects.42 One of AMPK’s benefits is to signal cells to consume stored fat. One way that AMPK performs this fat-removing process is by down-regulating mTOR.43

AMPK is a master energy sensor in cells.35 When AMPK is activated by compounds like Gynostemma pentaphyllum,35,44 cells think they are energy-deprived. The desired effect for most aging people is to prompt cells to turn down excess mTOR and utilize fat stores for energy production.

Balancing mTOR activity and autophagy can be achieved via increasing cellular AMPK in the following six ways:

  1. Reduce calorie intake and more specifically, avoid sugars and simple carbohydrates. High blood levels of glucose fuel excess mTOR activity.45
  2. Brief periods (3-5 days) of calorie restriction per month have shown great benefits indicative of balanced mTOR,46 but compliance is difficult.
  3. Consider “intermittent fasting” for 14-18 hours five days a week, based on voluminous data, including a fascinating report published in the December 26, 2019 issue of the New England Journal of Medicine.47
  4. Preclinical studies show that calorie restriction mimetics such as resveratrol and NAD+ can be used to support SIRT1 and FoxO function.26,48
  5. Increased physical activity can meaningfully boost AMPK.51

Rejuvenating Bone Marrow Stem Cells

The impact of boosting AMPK and lowering excess mTOR may enable rejuvenation of aging bone marrow (hematopoietic) stem cells. A safe way of balancing mTOR is to boost cellular AMPK activity. Increasing AMPK regulates mTOR, which facilitates removal of cellular debris (via autophagy).52,53

As it relates to combatting aging, activating autophagy appears to be a critical factor for the rejuvenation of aged hematopoietic stem cells.25 Hematopoietic stem cells are crucial for producing new immune cells, platelets, and red blood cells. Middle-aged and elderly people today have ready access to low-cost approaches to help preserve their bone marrow stem cell pools.

When the bone marrow stem cell niche becomes exhausted, life can no longer be sustained. That’s because oxygen-carrying red blood cells, immune-protecting white cells, and hemorrhage-guarding platelets must be continually produced in the bone marrow for systemic existence.

Increase SIRT1 with Resveratrol

Resveratrol activates SIRT1 inside cells, which is linked to many of the same longevity-enhancing benefits as calorie restriction.26

Based on our interpretation of emerging evidence, age control could be enhanced by modest doses of resveratrol, with adequate NAD+ replenishment to ensure sirtuin functionality. Most people over age 40 should initiate supplementation with the oral NAD+ precursor (nicotinamide riboside) in the daily dose of 300 mg to 600 mg, along with 100 mg to 300 mg of resveratrol and AMPK-activating compounds.

By targeting known regulators of stem cell self-renewal and differentiation, we are proposing a unique protocol to rejuvenate your own stem cells.

FACTORS THAT CONFER STEM CELL HEALTH

As it relates to stem cell regeneration, the following processes are intimately involved:

  1. DNA repair pathways affected by:58
    • SIRT1
    • NAD+
    • FoxO
  2. Protein synthesis affected by:55
    • AMPK
    • mTOR
    • FoxO
  3. Mitochondrial function affected by:59
    • SIRT1
    • NAD+
    • FoxO

Hallmarks of degenerative aging include dysregulation of AMPK, FoxO and SIRT1, depletion of NAD+, and excessive activation of mTOR.7,60 In what may be a unified approach to living healthier, the ability to reactivate aged stem cells is already being practiced by some enlightened people today. This includes those who take steps to balance AMPK, SIRT1, FoxO and NAD+ while normalizing excess mTOR.

Summary Overview

Adult stem cells lose their ability to repopulate tissues with fresh functional cells.

The result is a systemic deterioration of tissues throughout our aging bodies. Treatments that are currently being used to slow aging, such as boosting AMPK and sirtuins, appear likely to facilitate stem cell rejuvenation. Regulation of mTOR enhances the regenerative capacity of hematopoietic stem cells in aged mice.25 mTOR is hyperactive in the bone marrow stem cell niche of aged mice.25 Excess mTOR can be balanced by increasing AMPK. Published data indicate that agents that boost NAD+,19 sirtuins24,54 and FoxO,56 along with compounds that increase AMPK35,44 (and down-regulate mTOR6,25) may work together to improve stem cell function. It and other compounds that activate AMPK (like Gynostemma pentaphyllum) represent a potential option for the induction of stem cell rejuvenation in adult stem cell therapies. The combined application of these mechanistic approaches in clinical medical practice could induce systemic rejuvenation of dysfunctional stem cells.

References

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