npj Aging最新文献

{"title":"Cadmium, von Willebrand factor and vascular aging.","authors":"Xia Wang,&nbsp;Maria N Starodubtseva,&nbsp;Carolyn M Kapron,&nbsp;Ju Liu","doi":"10.1038/s41514-023-00107-3","DOIUrl":"https://doi.org/10.1038/s41514-023-00107-3","url":null,"abstract":"<p><p>Vascular aging is a major contributing factor to cardiovascular disease. The aged blood vessels, characterized by vascular wall thickening and stiffening, are instigated by endothelial cell dysfunction induced by oxidative stress and inflammation. von Willebrand Factor (vWF) is a glycoprotein known for its role in coagulation, and plasma levels of vWF are increased with age. Elevated vWF promotes thrombosis, atherosclerotic plaque formation, inflammation and proliferation of vascular smooth muscle cells. Cadmium (Cd) is an environmental pollutant associated with increased morbidity and mortality of cardiovascular disease. At low concentrations, Cd activates pro-survival signaling in endothelial cells, however enhances intima-media thickness and atherogenesis. A non-cytotoxic dose of Cd also increases endothelial vWF expression and secretion in vivo and in vitro. In this review, we summarize the molecular mechanisms underlying vWF-promoted vascular aging-associated pathologies and Cd-induced vWF expression. In addition, we propose that exposure to low-dose Cd is a risk factor for vascular aging, through elevation of plasma vWF.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"11"},"PeriodicalIF":0.0,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10235123/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9574017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Senotherapeutic peptide treatment reduces biological age and senescence burden in human skin models.","authors":"Alessandra Zonari, Lear E Brace, Kallie Al-Katib, William F Porto, Daniel Foyt, Mylieneth Guiang, Edgar Andres Ochoa Cruz, Bailey Marshall, Melissa Gentz, Gabriela Rapozo Guimarães, Octavio L Franco, Carolina R Oliveira, Mariana Boroni, Juliana L Carvalho","doi":"10.1038/s41514-023-00109-1","DOIUrl":"10.1038/s41514-023-00109-1","url":null,"abstract":"<p><p>Cellular senescence is known to play a role in age-related skin function deterioration which potentially influences longevity. Here, a two-step phenotypic screening was performed to identify senotherapeutic peptides, leading to the identification of Peptide (Pep) 14. Pep 14 effectively decreased human dermal fibroblast senescence burden induced by Hutchinson-Gilford Progeria Syndrome (HGPS), chronological aging, ultraviolet-B radiation (UVB), and etoposide treatment, without inducing significant toxicity. Pep 14 functions via modulation of PP2A, an understudied holoenzyme that promotes genomic stability and is involved in DNA repair and senescence pathways. At the single-cell level, Pep 14 modulates genes that prevent senescence progression by arresting the cell cycle and enhancing DNA repair, which consequently reduce the number of cells progressing to late senescence. When applied on aged ex vivo skin, Pep 14 promoted a healthy skin phenotype with structural and molecular resemblance to young ex vivo skin, decreased the expression of senescence markers, including SASP, and reduced the DNA methylation age. In summary, this work shows the safe reduction of the biological age of ex vivo human skins by a senomorphic peptide.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"10"},"PeriodicalIF":0.0,"publicationDate":"2023-05-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10203313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9568909","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Gut microbiota and circadian rhythm in Alzheimer's disease pathophysiology: a review and hypothesis on their association.","authors":"Mohammad Rafi Khezri,&nbsp;Morteza Ghasemnejad-Berenji","doi":"10.1038/s41514-023-00104-6","DOIUrl":"https://doi.org/10.1038/s41514-023-00104-6","url":null,"abstract":"<p><p>Alzheimer's disease (AD) is the most common neurodegenerative disease and the leading cause of dementia worldwide. Different pathologic changes have been introduced to be involved in its progression. Although amyloid-β (Aβ) deposition and tau hyperphosphorylation and aggregation are mainly considered the main characterizations of AD, several other processes are involved. In recent years, several other changes, including alterations in gut microbiota proportion and circadian rhythms, have been noticed due to their role in AD progression. However, the exact mechanism indicating the association between circadian rhythms and gut microbiota abundance has not been investigated yet. This paper aims to review the role of gut microbiota and circadian rhythm in AD pathophysiology and introduces a hypothesis to explain their association.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"9"},"PeriodicalIF":0.0,"publicationDate":"2023-05-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10154390/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9411376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Recent insights into the crosstalk between senescent cells and CD8 T lymphocytes.","authors":"Ines Marin, Manuel Serrano, Federico Pietrocola","doi":"10.1038/s41514-023-00105-5","DOIUrl":"10.1038/s41514-023-00105-5","url":null,"abstract":"","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"8"},"PeriodicalIF":0.0,"publicationDate":"2023-04-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073090/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9271001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Oral supplementation of nicotinamide riboside alters intestinal microbial composition in rats and mice, but not humans.","authors":"A Augusto Peluso,&nbsp;Agnete T Lundgaard,&nbsp;Parizad Babaei,&nbsp;Felippe Mousovich-Neto,&nbsp;Andréa L Rocha,&nbsp;Mads V Damgaard,&nbsp;Emilie G Bak,&nbsp;Thiyagarajan Gnanasekaran,&nbsp;Ole L Dollerup,&nbsp;Samuel A J Trammell,&nbsp;Thomas S Nielsen,&nbsp;Timo Kern,&nbsp;Caroline B Abild,&nbsp;Karolina Sulek,&nbsp;Tao Ma,&nbsp;Zach Gerhart-Hines,&nbsp;Matthew P Gillum,&nbsp;Manimozhiyan Arumugam,&nbsp;Cathrine Ørskov,&nbsp;Douglas McCloskey,&nbsp;Niels Jessen,&nbsp;Markus J Herrgård,&nbsp;Marcelo A S Mori,&nbsp;Jonas T Treebak","doi":"10.1038/s41514-023-00106-4","DOIUrl":"https://doi.org/10.1038/s41514-023-00106-4","url":null,"abstract":"<p><p>The gut microbiota impacts systemic levels of multiple metabolites including NAD⁺ precursors through diverse pathways. Nicotinamide riboside (NR) is an NAD⁺ precursor capable of regulating mammalian cellular metabolism. Some bacterial families express the NR-specific transporter, PnuC. We hypothesized that dietary NR supplementation would modify the gut microbiota across intestinal sections. We determined the effects of 12 weeks of NR supplementation on the microbiota composition of intestinal segments of high-fat diet-fed (HFD) rats. We also explored the effects of 12 weeks of NR supplementation on the gut microbiota in humans and mice. In rats, NR reduced fat mass and tended to decrease body weight. Interestingly, NR increased fat and energy absorption but only in HFD-fed rats. Moreover, 16S rRNA gene sequencing analysis of intestinal and fecal samples revealed an increased abundance of species within Erysipelotrichaceae and Ruminococcaceae families in response to NR. PnuC-positive bacterial strains within these families showed an increased growth rate when supplemented with NR. The abundance of species within the Lachnospiraceae family decreased in response to HFD irrespective of NR. Alpha and beta diversity and bacterial composition of the human fecal microbiota were unaltered by NR, but in mice, the fecal abundance of species within Lachnospiraceae increased while abundances of Parasutterella and Bacteroides dorei species decreased in response to NR. In conclusion, oral NR altered the gut microbiota in rats and mice, but not in humans. In addition, NR attenuated body fat mass gain in rats, and increased fat and energy absorption in the HFD context.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"7"},"PeriodicalIF":0.0,"publicationDate":"2023-04-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10070358/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9624877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Aging reduces calreticulin expression and alters spontaneous calcium signals in astrocytic endfeet of the mouse dorsolateral striatum.","authors":"Sara M Zarate,&nbsp;Taylor E Huntington,&nbsp;Pooneh Bagher,&nbsp;Rahul Srinivasan","doi":"10.1038/s41514-023-00102-8","DOIUrl":"https://doi.org/10.1038/s41514-023-00102-8","url":null,"abstract":"<p><p>Aging-related impairment of the blood brain barrier (BBB) and neurovascular unit (NVU) increases the risk for neurodegeneration. Among various cells that participate in BBB and NVU function, calcium signals in astrocytic endfeet are crucial for maintaining BBB and NVU integrity. To assess if aging is associated with altered calcium signals within astrocytic endfeet of the dorsolateral striatum (DLS), we expressed GCaMP6f in DLS astrocytes of young (3-4 months), middle-aged (12-15 months) and aging (20-30 months) mice. Compared to endfeet in young mice, DLS endfeet in aging mice demonstrated decreased calreticulin expression, and alterations to both spontaneous membrane-associated and mitochondrial calcium signals. While young mice required both extracellular and endoplasmic reticulum calcium sources for endfoot signals, middle-aged and aging mice showed heavy dependence on endoplasmic reticulum calcium. Thus, astrocytic endfeet show significant changes in calcium buffering and sources throughout the lifespan, which is important for understanding mechanisms by which aging impairs the BBB and NVU.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"5"},"PeriodicalIF":0.0,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066375/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9650927","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Author Correction: How does hormesis impact biology, toxicology, and medicine?","authors":"Edward J Calabrese,&nbsp;Mark P Mattson","doi":"10.1038/s41514-023-00101-9","DOIUrl":"https://doi.org/10.1038/s41514-023-00101-9","url":null,"abstract":"","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"6"},"PeriodicalIF":0.0,"publicationDate":"2023-03-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10066356/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9288248","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Factors for optimizing intervention programs for cognition in older adults: the value of exergames.","authors":"Alexandra Perrot,&nbsp;Pauline Maillot","doi":"10.1038/s41514-023-00103-7","DOIUrl":"https://doi.org/10.1038/s41514-023-00103-7","url":null,"abstract":"<p><p>This review presents factors that could optimize the effectiveness of an intervention program on cognitive health in older adults. Combined, multi-dimensional and interactive programs appear to be relevant. On one hand, for the characteristics to be implemented in the physical dimension of a program, multimodal interventions stimulating the aerobic pathway and muscle strengthening during the solicitation of gross motor activities, seem to be interesting. On the other hand, regarding the cognitive dimension of a program, complex and variable cognitive stimuli appear to hold the greatest promise for generating cognitive benefits and the broadest transfers to untrained tasks. The field of video games also brings interesting enrichment through the gamification of situations and the feeling of immersion. However, some gray areas remain to be clarified, notably the ideal response dose, the balance between physical and cognitive solicitation and the programs' customization.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"4"},"PeriodicalIF":0.0,"publicationDate":"2023-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060229/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9216423","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Long-term intensive endurance exercise training is associated to reduced markers of cellular senescence in the colon mucosa of older adults.","authors":"Marco Demaria,&nbsp;Beatrice Bertozzi,&nbsp;Nicola Veronese,&nbsp;Francesco Spelta,&nbsp;Edda Cava,&nbsp;Valeria Tosti,&nbsp;Laura Piccio,&nbsp;Dayna S Early,&nbsp;Luigi Fontana","doi":"10.1038/s41514-023-00100-w","DOIUrl":"https://doi.org/10.1038/s41514-023-00100-w","url":null,"abstract":"<p><p>Regular endurance exercise training is an effective intervention for the maintenance of metabolic health and the prevention of many age-associated chronic diseases. Several metabolic and inflammatory factors are involved in the health-promoting effects of exercise training, but regulatory mechanisms remain poorly understood. Cellular senescence-a state of irreversible growth arrest-is considered a basic mechanism of aging. Senescent cells accumulate over time and promote a variety of age-related pathologies from neurodegenerative disorders to cancer. Whether long-term intensive exercise training affect the accumulation of age-associated cellular senescence is still unclear. Here, we show that the classical senescence markers p16 and IL-6 were markedly higher in the colon mucosa of middle-aged and older overweight adults than in young sedentary individuals, but this upregulation was significantly blunted in age-matched endurance runners. Interestingly, we observe a linear correlation between the level of p16 and the triglycerides to HDL ratio, a marker of colon adenoma risk and cardiometabolic dysfunction. Our data suggest that chronic high-volume high-intensity endurance exercise can play a role in preventing the accumulation of senescent cells in cancer-prone tissues like colon mucosa with age. Future studies are warranted to elucidate if other tissues are also affected, and what are the molecular and cellular mechanisms that mediate the senopreventative effects of different forms of exercise training.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"3"},"PeriodicalIF":0.0,"publicationDate":"2023-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971019/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10872189","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Increased activity of lacrimal gland mast cells are associated with corneal epitheliopathy in aged mice.","authors":"Elsayed Elbasiony, WonKyung J Cho, Aastha Singh, Sharad K Mittal, Driss Zoukhri, Sunil K Chauhan","doi":"10.1038/s41514-023-00099-0","DOIUrl":"10.1038/s41514-023-00099-0","url":null,"abstract":"<p><p>The lacrimal gland undergoes significant structural and functional deterioration with aging. Marked with increased inflammation and fibrosis, the aged lacrimal gland is unable to perform its protective function. As a result, the ocular surface becomes highly susceptible to various ocular surface pathologies, including corneal epitheliopathy. We and others have previously shown that mast cells mediate tissue inflammation by recruiting other immune cells. However, despite their well-known characteristics of secreting various inflammatory mediators, whether mast cells contribute to the immune cell aggregation and activation, and acinar dystrophy of the aged lacrimal gland has not been investigated. Here, we demonstrate the role of mast cells in age-related lacrimal gland pathophysiology using mast cell-deficient (cKit^w-sh) mice. Our data demonstrated a significant increase in mast cell frequencies and immune cell infiltration in the lacrimal gland of aged mice. Interestingly, mast cell deficiency resulted in a substantial reduction in inflammation and preservation of lacrimal gland structure, suggesting that mast cells mediate the aging process of the lacrimal gland.</p>","PeriodicalId":19348,"journal":{"name":"npj Aging","volume":"9 1","pages":"2"},"PeriodicalIF":0.0,"publicationDate":"2023-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9971332/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9362556","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}