Faculty Opinions recommendation of Dietary Restriction Extends Lifespan through Metabolic Regulation of Innate Immunity.

Author(s):  
Thomas Flatt
2021 ◽  
Vol 33 (10) ◽  
pp. 2090
Author(s):  
Ziyun Wu ◽  
Meltem Isik ◽  
Natalie Moroz ◽  
Michael J. Steinbaugh ◽  
Peng Zhang ◽  
...  

2019 ◽  
Vol 29 (5) ◽  
pp. 1192-1205.e8 ◽  
Author(s):  
Ziyun Wu ◽  
Meltem Isik ◽  
Natalie Moroz ◽  
Michael J. Steinbaugh ◽  
Peng Zhang ◽  
...  

2021 ◽  
Author(s):  
Chayki Charar ◽  
Sally Metsuyanim-Cohen ◽  
Daniel Z. Bar

Animals subjected to dietary restriction (DR) have reduced body size, low fecundity, slower development, lower fat content and longer life span. We identified lamin as a regulator of multiple dietary restriction phenotypes. Downregulation of lmn-1, the single Caenorhabditis elegans lamin gene, increased animal size and fat content, specifically in DR animals. The LMN-1 protein acts in the mTOR pathway, upstream to RAPTOR and S6K, key component and target of mTOR complex 1 (mTORC1), respectively. DR excludes the mTORC1 activator RAGC-1 from the nucleus. Downregulation of lmn-1 restores RAGC-1 to the nucleus, a necessary step for the activation of the mTOR pathway. These findings further link lamin to metabolic regulation.


Author(s):  
Samin Ayromlou ◽  
Leila Sadat Hatamnezhad ◽  
Hormoz Ayromlou ◽  
Siamak Sandoghchian Shotorbani

Author(s):  
Shaonan Liang ◽  
Liangliang Ji ◽  
Lan Kang ◽  
Xiaoyu Hu

Author(s):  
Andrea Keller ◽  
Tyus Temple ◽  
Behnam Sayanjali ◽  
Maria M. Mihaylova

AbstractPurpose of ReviewFrom invertebrates to vertebrates, the ability to sense nutrient availability is critical for survival. Complex organisms have evolved numerous signaling pathways to sense nutrients and dietary fluctuations, which influence many cellular processes. Although both overabundance and extreme depletion of nutrients can lead to deleterious effects, dietary restriction without malnutrition can increase lifespan and promote overall health in many model organisms. In this review, we focus on age-dependent changes in stem cell metabolism and dietary interventions used to modulate stem cell function in aging.Recent FindingsOver the last half-century, seminal studies have illustrated that dietary restriction confers beneficial effects on longevity in many model organisms. Many researchers have now turned to dissecting the molecular mechanisms by which these diets affect aging at the cellular level. One subpopulation of cells of particular interest are adult stem cells, the most regenerative cells of the body. It is generally accepted that the regenerative capacity of stem cells declines with age, and while the metabolic requirements of each vary across tissues, the ability of dietary interventions to influence stem cell function is striking.SummaryIn this review, we will focus primarily on how metabolism plays a role in adult stem cell homeostasis with respect to aging, with particular emphasis on intestinal stem cells while also touching on hematopoietic, skeletal muscle, and neural stem cells. We will also discuss key metabolic signaling pathways influenced by both dietary restriction and the aging process, and will examine their role in improving tissue homeostasis and lifespan. Understanding the mechanisms behind the metabolic needs of stem cells will help bridge the divide between a basic science interpretation of stem cell function and a whole-organism view of nutrition, thereby providing insight into potential dietary or therapeutic interventions.


Cell Reports ◽  
2017 ◽  
Vol 20 (2) ◽  
pp. 479-490 ◽  
Author(s):  
Jung-Eun Lee ◽  
Morsi Rayyan ◽  
Allison Liao ◽  
Isaac Edery ◽  
Scott D. Pletcher

2019 ◽  
Vol 116 (37) ◽  
pp. 18647-18654 ◽  
Author(s):  
Christopher Monit ◽  
Elizabeth R. Morris ◽  
Christopher Ruis ◽  
Bart Szafran ◽  
Grant Thiltgen ◽  
...  

The vertebrate protein SAMHD1 is highly unusual in having roles in cellular metabolic regulation, antiviral restriction, and regulation of innate immunity. Its deoxynucleoside triphosphohydrolase activity regulates cellular dNTP concentration, reducing levels below those required by lentiviruses and other viruses to replicate. To counter this threat, some primate lentiviruses encode accessory proteins that bind SAMHD1 and induce its degradation; in turn, positive diversifying selection has been observed in regions bound by these lentiviral proteins, suggesting that primate SAMHD1 has coevolved to evade these countermeasures. Moreover, deleterious polymorphisms in humanSAMHD1are associated with autoimmune disease linked to uncontrolled DNA synthesis of endogenous retroelements. Little is known about how evolutionary pressures affect these different SAMHD1 functions. Here, we examine the deeper history of these interactions by testing whether evolutionary signatures in SAMHD1 extend to other mammalian groups and exploring the molecular basis of this coevolution. Using codon-based likelihood models, we find positive selection in SAMHD1 within each mammal lineage for which sequence data are available. We observe positive selection at sites clustered around T592, a residue that is phosphorylated to regulate SAMHD1 activity. We verify experimentally that mutations within this cluster affect catalytic rate and lentiviral restriction, suggesting that virus–host coevolution has required adaptations of enzymatic function. Thus, persistent positive selection may have involved the adaptation of SAMHD1 regulation to balance antiviral, metabolic, and innate immunity functions.


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