Shirakawa and Sano reviewed T cell immunosenescence in the context of aging, obesity, and cardiovascular disease in the journal Cells in 2021.
Restoring defective intercellular communications by inhibiting inflammation can rejuvenate aging-impaired changes, though long-term inflammation inhibition may result in immunosuppression.
The role of damage to DNA and other macromolecules in aging is discussed in the 2009 paper 'Does damage to DNA and other macromolecules play a role in aging? If so, how?' published in The Journals of Gerontology: Series A.
Angeli, S. et al. published a study in 2021 titled 'The mitochondrial permeability transition pore activates the mitochondrial unfolded protein response and promotes aging' in eLife, which establishes that the mitochondrial permeability transition pore triggers the mitochondrial unfolded protein response and contributes to the aging process.
Lin et al. (2021) described the dynamic regulation of mitochondrial-endoplasmic reticulum crosstalk during stem cell homeostasis and aging.
Inflammation, epigenetics, and metabolism converge to influence cell senescence and aging, as described by Zhu et al. in a 2021 Signal Transduction and Targeted Therapy paper.
Microenvironmental changes with aging may disrupt multicellular organization and favor the cancer cell phenotype, as proposed by Castillo, Keymer, and Marquet in their 2021 BioEssays paper.
The Wnt signaling pathway has a dual role during aging in Caenorhabditis elegans.
Conde-Perezprina, J. C., Leon-Galvan, M. A., and Konigsberg, M. published a study in 2012 titled 'DNA mismatch repair system: repercussions in cellular homeostasis and relationship with aging' in Oxidative Medicine and Cellular Longevity, which examines the role of the DNA mismatch repair system in cellular homeostasis and its connection to aging.
Rea, I. M. et al. published a study in 2018 titled 'Age and age-related diseases: role of inflammation triggers and cytokines' in Frontiers in Immunology, which examines the role of inflammation triggers and cytokines in aging and age-related diseases.
Hodge B. A. et al. found that dietary restriction and the transcription factor clock delay eye aging to extend lifespan in Drosophila Melanogaster, as reported in a 2022 study in Nature Communications.
Libby, P. and Kobold, S. published a study in 2019 titled 'Inflammation: a common contributor to cancer, aging, and cardiovascular diseases-expanding the concept of cardio-oncology' in Cardiovascular Research, which posits inflammation as a common factor contributing to cancer, aging, and cardiovascular diseases.
Autophagy and the lysosomal degradative system play a central role in aging, according to Rajawat, Hilioti, and Bossis in their 2009 Ageing Research Reviews paper.
Stem cell therapy is considered a promising rejuvenative strategy for reversing aging and alleviating diseases.
Wnt signaling is involved in bone, kidney, intestine, and adipose tissue maintenance and interorgan interaction during aging.
Royce, G. H., Brown-Borg, H. M., and Deepa, S. S. published a study in 2019 titled 'The potential role of necroptosis in inflammaging and aging' in Geroscience, which explores the potential involvement of necroptosis in the processes of inflammaging and aging.
Adler A. S. et al. revealed that a motif module map shows the enforcement of aging by continual NF-kappaB activity in a 2007 study published in Genes & Development.
Circadian timing is important for aging and longevity, according to Acosta-Rodriguez et al. in Nature Communications (2021).
Liang et al. (2020) published 'Circadian regulation of adult stem cell homeostasis and aging' in Cell Stem Cell, detailing how circadian rhythms influence adult stem cell maintenance and the aging process.
The 'Cell membrane theory of senescence' and the role of bioactive lipids in aging and associated diseases are discussed in the 2021 paper '“Cell membrane theory of senescence” and the role of bioactive lipids in aging, and aging associated diseases and their therapeutic implications' published in Biomolecules.
Circadian rhythms change during aging, impacting later life, as reviewed by Hood and Amir in the Journal of Clinical Investigation (2017).
Yamashita and Iwama reviewed the aging and clonal behavior of hematopoietic stem cells in the International Journal of Molecular Sciences in 2022.
The relationship between telomeres and aging is examined in the 2018 paper 'Telomeres and aging' published in Current Opinion in Cell Biology.
The relationship between epigenetics and aging is reviewed in the 2013 paper 'Epigenetics and aging' published in Maturitas.
The extracellular matrix plays a central role in aging and osteoarthritis, according to Rahmati et al. in their research.
Dierickx et al. (2022) published 'Aging disrupts circadian gene regulation and function in macrophages' in Nature Immunology, demonstrating that aging impairs circadian mechanisms in immune cells.
Montaruli et al. (2020) published 'The wrinkling of time: Aging, inflammation, oxidative stress, and the circadian clock in neurodegeneration' in Neurobiology of Disease, examining the intersection of aging, inflammation, and circadian rhythms in neurodegenerative conditions.
Deep proteomic analysis of large-scale populations confirms that plasma proteins sclerostin, pleiotrophin, and transgelin increase with aging, while epidermal growth factor receptor (ERBB1) and α2-antiplasmin decrease with age.
Aging exacerbates ribosome pausing, which disrupts cotranslational proteostasis, according to the 2022 paper 'Ageing exacerbates ribosome pausing to disrupt cotranslational proteostasis' published in Nature.
Swer and Sharma (2021) reviewed the role of ATP-dependent chromatin remodelers in the processes of aging and age-related disorders.
Metabolomic analysis identifies blood metabolic profiles that change with aging or aging-relevant conditions.
Schuler et al. (2021) reported that extensive remodeling of the extracellular matrix during aging contributes to age-dependent impairments of muscle stem cell functionality.
Energy metabolism and aging in mice are linked, as reviewed by Azzu and Valencak in their 2017 Gerontology paper.
AMP-activated protein kinase (AMPK) regulates the NLRP3 inflammasome during aging, as discussed in a 2018 review by Cordero et al. in Trends in Endocrinology & Metabolism.
FOXO proteins play a role in aging and longevity, as detailed in the 2016 paper 'Long live FOXO: unraveling the role of FOXO proteins in aging and longevity' published in Aging Cell.
H. Zhang, K. J. A. Davies, and H. J. Forman reviewed the oxidative stress response and Nrf2 signaling in aging in Free Radic. Biol. Med. (2015).
Cellular senescence and its potential role in tumor promotion and aging are examined in the 2016 paper 'Cellular senescence and tumor promotion: Is aging the key?' published in Biochimica et Biophysica Acta.
JAK2 plays roles in aging, inflammation, hematopoiesis, and malignant transformation.
Polyphenols can target the Wnt signaling pathway, with implications for aging and age-related diseases.
The relationship between proteostasis, oxidative stress, and aging is reviewed in the 2017 paper 'Proteostasis, oxidative stress and aging' published in Redox Biology.
Pathways of cellular proteostasis in aging and disease are described in the 2018 paper 'Pathways of cellular proteostasis in aging and disease' published in the Journal of Cell Biology.
H. Zhang, K. J. Menzies, and J. Auwerx reviewed the role of mitochondria in stem cell fate and aging in Development (2018).
Mitochondria play a role in skin health, aging, and disease, as reported by Sreedhar, Aguilera-Aguirre, and Singh in their 2020 Cell Death & Disease paper.
Tam, Morais, and Santosa (2020) discussed the relationship between obesity and aging, characterizing them as two sides of the same coin.
Targeting tissue-specific metabolic signaling pathways in aging presents both promises and limitations, as reviewed by Zhong et al. in a 2014 article in Protein & Cell.
Liu, R. M. discusses aging, cellular senescence, and Alzheimer’s disease in the International Journal of Molecular Sciences.
Noncoding RNAs control telomere homeostasis in senescence and aging, as discussed in the 2020 paper 'Noncoding RNAs controlling telomere homeostasis in senescence and aging' published in Trends in Molecular Medicine.
Sirtuins, melatonin, and circadian rhythms are interconnected in the context of aging and cancer, as discussed by Jung-Hynes, Reiter, and Ahmad in the Journal of Pineal Research (2010).
AMPK-mediated pathways play a role in autophagy and aging, according to a 2022 review by Ge et al. in Biochimie.
Lananna and Musiek (2015) published 'The circadian clock in skin: implications for adult stem cells, tissue regeneration, cancer, aging, and immunity' in Journal of Biological Rhythms, detailing the role of circadian clocks in skin physiology.
Lipid assemblies are at the intersection of aging, proteostasis, and neurodegeneration, as described in the 2019 paper 'Lipid assemblies at the crossroads of aging, proteostasis, and neurodegeneration' published in Trends in Cell Biology.
Menendez and Alarcon (2017) discuss the senescence-inflammatory regulation of reparative cellular reprogramming in the contexts of aging and cancer.
Picca et al. (2019) analyzed extracellular vesicles to gain insights into mitochondrial dysfunction and aging.
Aging alters bone-fat reciprocity by shifting in vivo mesenchymal precursor cell fate towards an adipogenic lineage, according to Singh et al. in their 2016 Bone paper.
Longevity-promoting pathways and transcription factors respond to and control extracellular matrix dynamics during aging and disease, as discussed by Vidovic and Ewald in their 2022 Frontiers in Aging paper.