A Panoramic View of Cell Population Dynamics in Mammalian Aging DOI Creative Commons
Zehao Zhang, Chloe Schaefer,

Weirong Jiang

et al.

bioRxiv (Cold Spring Harbor Laboratory), Journal Year: 2024, Volume and Issue: unknown

Published: March 5, 2024

Abstract To elucidate the aging-associated cellular population dynamics throughout body, here we present PanSci, a single-cell transcriptome atlas profiling over 20 million cells from 623 mouse tissue samples, encompassing range of organs across different life stages, sexes, and genotypes. This comprehensive dataset allowed us to identify more than 3,000 unique states catalog 200 distinct cell populations experiencing significant depletion or expansion. Our panoramic analysis uncovered temporally structured, organ- lineage-specific shifts during lifespan progression. Moreover, investigated alterations in immune populations, revealing both widespread organ-specific changes. We further explored regulatory roles system on aging pinpointed specific age-related expansions that are lymphocyte-dependent. The breadth depth our ‘cell-omics’ methodology not only enhance comprehension but also lay groundwork for exploring complex networks among varied types context diseases. One Sentence Summary lifespan, unveils temporal architecture dynamics, shifts, lymphocyte’s role organismal aging.

Language: Английский

Stress, epigenetics, and aging: Unraveling the intricate crosstalk DOI Creative Commons
Zeming Wu, Jing Qu, Weiqi Zhang

et al.

Molecular Cell, Journal Year: 2023, Volume and Issue: 84(1), P. 34 - 54

Published: Nov. 13, 2023

Language: Английский

Citations

54

Emerging epigenetic insights into aging mechanisms and interventions DOI
Zeming Wu, Weiqi Zhang, Jing Qu

et al.

Trends in Pharmacological Sciences, Journal Year: 2024, Volume and Issue: 45(2), P. 157 - 172

Published: Jan. 11, 2024

Language: Английский

Citations

20

Aging and the emerging role of cellular senescence in osteoarthritis DOI
Brian O. Diekman, Richard F. Loeser

Osteoarthritis and Cartilage, Journal Year: 2023, Volume and Issue: 32(4), P. 365 - 371

Published: Dec. 2, 2023

Language: Английский

Citations

24

Roles of chromatin and genome instability in cellular senescence and their relevance to ageing and related diseases DOI
Zeming Wu, Jing Qu, Guang‐Hui Liu

et al.

Nature Reviews Molecular Cell Biology, Journal Year: 2024, Volume and Issue: 25(12), P. 979 - 1000

Published: Oct. 3, 2024

Language: Английский

Citations

9

Insights and Interventions in Age-Associated Inflammation DOI
Haoyan Huang, Jie Ren, Guang‐Hui Liu

et al.

Current Opinion in Genetics & Development, Journal Year: 2025, Volume and Issue: 91, P. 102306 - 102306

Published: Jan. 20, 2025

Language: Английский

Citations

1

The intersection of aging and estrogen in osteoarthritis DOI Creative Commons
Aysegul Atasoy‐Zeybek,

Kelly K. Showel,

Christopher V. Nagelli

et al.

npj Women s Health, Journal Year: 2025, Volume and Issue: 3(1)

Published: Feb. 25, 2025

Osteoarthritis (OA) is a chronic joint disease characterized by cartilage degradation, inflammation, and pain. While multiple factors contribute to OA development, age sex are primary risk factors, particularly affecting postmenopausal women. The dramatic increase in after menopause suggests estrogen deficiency accelerates progression. This review explores the molecular mechanisms connecting aging focusing on key genes pathways identified through RNA sequencing.

Language: Английский

Citations

1

Longevity biotechnology: bridging AI, biomarkers, geroscience and clinical applications for healthy longevity DOI Creative Commons
Yihua Lyu, Qiang Fu, Dominika Wilczok

et al.

Aging, Journal Year: 2024, Volume and Issue: unknown

Published: Oct. 16, 2024

Aging | doi:10.18632/aging.206135. Yu-Xuan Lyu, Qiang Fu, Dominika Wilczok, Kejun Ying, Aaron King, Adam Antebi, Aleksandar Vojta, Alexandra Stolzing, Alexey Moskalev, Anastasia Georgievskaya, Andrea B. Maier, Olsen, Anja Groth, Anna Katharina Simon, Anne Brunet, Aisyah Jamil, Anton Kulaga, Asif Bhatti, Benjamin Yaden, Bente Klarlund Pedersen, Björn Schumacher, Boris Djordjevic, Brian Kennedy, Chieh Chen, Christine Yuan Huang, Christoph U. Correll, Coleen T. Murphy, Collin Y. Ewald, Danica Dario Riccardo Valenzano, Dariusz Sołdacki, David Erritzoe, Meyer, A. Sinclair, Eduardo Nunes Chini, Emma C. Teeling, Eric Morgen, Verdin, Erik Vernet, Estefano Pinilla, Evandro F. Fang, Evelyne Bischof, Evi M. Mercken, Fabian Finger, Folkert Kuipers, Frank W. Pun, Gabor Gyülveszi, Gabriele Civiletto, Garri Zmudze, Gil Blander, Harold Pincus, Joshua McClure, James L. Kirkland, Peyer, Jamie N. Justice, Jan Vijg, Jennifer R. Gruhn, Jerry McLaughlin, Joan Mannick, João Passos, Joseph Baur, Joe Betts-LaCroix, John Sedivy, Speakman, Jordan Shlain, Julia von Maltzahn, Katrin I. Andreasson, Kelsey Moody, Konstantinos Palikaras, Kristen Fortney, Laura J. Niedernhofer, Lene Juel Rasmussen, Liesbeth Veenhoff, Lisa Melton, Luigi Ferrucci, Marco Quarta, Maria Koval, Marinova, Mark Hamalainen, Maximilian Unfried, Michael S. Ringel, Milos Filipovic, Mourad Topors, Natalia Mitin, Nawal Roy, Nika Pintar, Nir Barzilai, Paolo Binetti, Parminder Singh, Paul Kohlhaas, D. Robbins, Rubin, Peter O. Fedichev, Petrina Kamya, Pura Muñoz-Canoves, Rafael de Cabo, Richard G. Faragher, Rob Konrad, Roberto Ripa, Robin Mansukhani, Sabrina Büttner, Sara Wickström, Sebastian Brunemeier, Sergey Jakimov, Shan Luo, Sharon Rosenzweig-Lipson, Shih-Yin Tsai, Stefanie Dimmeler, Thomas Rando, Tim Peterson, Tina Woods, Tony Wyss-Coray, Toren Finkel, Tzipora Strauss, Vadim Gladyshev, Valter Longo, Varun Dwaraka, Vera Gorbunova, Victoria Acosta-Rodríguez, Vincenzo Sorrentino, Vittorio Sebastiano, Wenbin Li, Yousin Suh, Alex Zhavoronkov, Morten Scheibye-Knudsen, Daniela Bakula

Language: Английский

Citations

8

Therapeutic strategies targeting cellular senescence for cancer and other diseases DOI Creative Commons
Xuebing Wang, Takeshi Fukumoto, Ken-ichi Noma

et al.

The Journal of Biochemistry, Journal Year: 2024, Volume and Issue: 175(5), P. 525 - 537

Published: Feb. 15, 2024

Abstract Cellular senescence occurs in response to endogenous or exogenous stresses and is characterized by stable cell cycle arrest, alterations nuclear morphology secretion of proinflammatory factors, referred as the senescence-associated secretory phenotype (SASP). An increase senescent cells associated with development several types cancer aging-related diseases. Therefore, senolytic agents that selectively remove may offer opportunities for developing new therapeutic strategies against such cancers This review outlines inducers general characteristics cells. We also discuss involvement certain Finally, we describe a series their utilization strategies.

Language: Английский

Citations

6

A panoramic view of cell population dynamics in mammalian aging DOI
Zehao Zhang, Chloe Schaefer,

Weirong Jiang

et al.

Science, Journal Year: 2024, Volume and Issue: unknown

Published: Nov. 28, 2024

To elucidate aging-associated cellular population dynamics, we present PanSci , a single-cell transcriptome atlas profiling over 20 million cells from 623 mouse tissues across different life stages, sexes, and genotypes. This comprehensive dataset reveals more than 3,000 unique states 200 cell populations. Our panoramic analysis uncovered organ-, lineage-, sex-specific shifts of dynamics during lifespan progression. Moreover, identify both systematic organ-specific alterations in immune populations associated with aging. We further explored the regulatory roles system on aging pinpointed specific age-related expansions that are lymphocyte dependent. “cell-omics” strategy enhances comprehension lays groundwork for exploring complex networks diseases.

Language: Английский

Citations

6

Emerging technology has a brilliant future: the CRISPR-Cas system for senescence, inflammation, and cartilage repair in osteoarthritis DOI Creative Commons
Shicheng Jia,

Rongji Liang,

Jiayou Chen

et al.

Cellular & Molecular Biology Letters, Journal Year: 2024, Volume and Issue: 29(1)

Published: May 2, 2024

Abstract Osteoarthritis (OA), known as one of the most common types aseptic inflammation musculoskeletal system, is characterized by chronic pain and whole-joint lesions. With cellular molecular changes including senescence, inflammatory alterations, subsequent cartilage defects, OA eventually leads to a series adverse outcomes such disability. CRISPR-Cas-related technology has been proposed explored gene therapy, offering potential gene-editing tools that are in spotlight. Considering genetic multigene regulatory mechanisms OA, we systematically review current studies on CRISPR-Cas for improving terms inflammation, damage summarize various strategies delivering CRISPR products, hoping provide new perspective treatment taking advantage technology.

Language: Английский

Citations

5