4.7 Article

Transplanting cells from old but not young donors causes physical dysfunction in older recipients

期刊

AGING CELL
卷 19, 期 3, 页码 -

出版社

WILEY
DOI: 10.1111/acel.13106

关键词

aging; cellular senescence; frailty; regenerative medicine

资金

  1. American Federation for Aging Research
  2. National Institute on Aging [AG13925, P01AG 62413-1, AG49182]

向作者/读者索取更多资源

Adipose-derived mesenchymal stem cell (ADSC)-based regenerative therapies have shown potential for use in many chronic diseases. Aging diminishes stem cell regenerative potential, yet it is unknown whether stem cells from aged donors cause adverse effects in recipients. ADSCs can be obtained using minimally invasive approaches and possess low immunogenicity. Nevertheless, we found that transplanting ADSCs from old donors, but not those from young donors, induces physical dysfunction in older recipient mice. Using single-cell transcriptomic analysis, we identified a naturally occurring senescent cell-like population in ADSCs primarily from old donors that resembles in vitro-generated senescent cells with regard to a number of key pathways. Our study reveals a previously unrecognized health concern due to ADSCs from old donors and lays the foundation for a new avenue of research to devise interventions to reduce harmful effects of ADSCs from old donors.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Geriatrics & Gerontology

Increased Levels of Circulating Cell-Free mtDNA in the Plasma of Subjects With Late-Life Depression and Frailty: A Preliminary Study

Emi Ampo, Ana Paula Mendes-Silva, Vanessa Goncalves, Jenna M. Bartley, George A. Kuchel, Breno S. Diniz

Summary: This study evaluated the levels of circulating cell-free mitochondrial DNA (ccf-mtDNA), a marker of cellular stress and damage, in older adults with late-life depression (LLD) and frailty. The coexistence of LLD and frailty was associated with higher levels of ccf-mtDNA, suggesting a common biological mechanism of cellular stress and mitochondrial dysfunction. This finding offers potential opportunities for future interventions guided by geroscience.

AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY (2022)

Article Multidisciplinary Sciences

Extending human healthspan and longevity: a symposium report

Loren M. DeVito, Nir Barzilai, Ana Maria Cuervo, Laura J. Niedernhofer, Sofiya Milman, Morgan Levine, Daniel Promislow, Luigi Ferrucci, George A. Kuchel, Joan Mannick, Jamie Justice, Mitzi M. Gonzales, James L. Kirkland, Pinchas Cohen, Judith Campisi

Summary: Geroscience posits that aging is malleable and by targeting the hallmarks of biological aging, age-related diseases can be alleviated and longevity extended. Experts have made significant advancements in understanding the mechanisms underlying biological aging and identified ways to target aging pathways. Proof-of-concept studies and early-stage clinical trials are underway to assess the feasibility of drug evaluation in geroscience.

ANNALS OF THE NEW YORK ACADEMY OF SCIENCES (2022)

Article Cell Biology

Senescence-induced changes in CD4 T cell differentiation can be alleviated by treatment with senolytics

Erica C. Lorenzo, Blake L. Torrance, Spencer R. Keilich, Iman Al-Naggar, Andrew Harrison, Ming Xu, Jenna M. Bartley, Laura Haynes

Summary: The differentiation of CD4 T helper cells during influenza infection is affected by aging, with an increase in regulatory T cells (Treg) and higher levels of TGF-beta in the lungs of aged mice. Treatment with senolytic drugs in aged mice prior to infection can restore Th cell differentiation and promote a return to homeostasis by reducing the percentage of Treg cells and inducing a healing Type 2 phenotype. Senescent cells play a significant role in impacting Th cell differentiation through production of cytokines like TGF-beta.

AGING CELL (2022)

Article Cell Biology

Targeting p21Cip1 highly expressing cells in adipose tissue alleviates insulin resistance in obesity

Lichao Wang, Binsheng Wang, Nathan S. Gasek, Yueying Zhou, Rachel L. Cohn, Dominique E. Martin, Wulin Zuo, William F. Flynn, Chun Guo, Evan R. Jellison, Taewan Kim, Larissa G. P. Langhi Prata, Allyson K. Palmer, Ming Li, Christina L. Inman, Lauren S. Barber, Iman M. A. Al-Naggar, Yanjiao Zhou, Wenqiang Du, Kshitiz, George A. Kuchel, Alexander Meves, Tamar Tchkonia, James L. Kirkland, Paul Robson, Ming Xu

Summary: This study identifies a small population of p21 high-expressing cells that accumulate in adipose tissue with obesity and shows that intermittent clearance of these cells can prevent and alleviate insulin resistance. Inactivation of the NF-kB pathway within these cells attenuates insulin resistance. Additionally, a drug combination of dasatinib and quercetin can eliminate p21 high-expressing cells in human fat and mitigate insulin resistance.

CELL METABOLISM (2022)

Review Cell Biology

The heterogeneity of cellular senescence: insights at the single-cell level

Rachel L. Cohn, Nathan S. Gasek, George A. Kuchel, Ming Xu

Summary: Senescent cells play a significant role in aging and disease, and targeting them could slow down the aging process. The commonly used marker p16 has led to important discoveries, but new markers and investigating heterogeneity are crucial. Advanced technologies like single-cell RNA-seq can help uncover new markers and the urgent need to investigate senescence heterogeneity.

TRENDS IN CELL BIOLOGY (2023)

Editorial Material Oncology

A path to translation: How 3D patient tumor avatars enable next generation precision oncology

Shree Bose, Margarida Barroso, Milan G. Chheda, Hans Clevers, Elena Elez, Salma Kaochar, Scott E. Kopetz, Xiao-Nan Li, Funda Meric-Bernstam, Clifford A. Meyer, Haiwei Mou, Kristen M. Naegle, Martin F. Pera, Zinaida Perova, Katerina A. Politi, Benjamin J. Raphael, Paul Robson, Rosalie C. Sears, Josep Tabernero, David A. Tuveson, Alana L. Welm, Bryan E. Welm, Christopher D. Willey, Konstantin Salnikow, Jeffrey H. Chuang, Xiling Shen

Summary: 3D patient tumor avatars hold great promise for precision medicine, but their clinical benefits need to be established through standardization and prospective trials. Innovative trial designs and integrated platforms combining diagnostics and therapeutics can accelerate the development of new treatments for refractory diseases.

CANCER CELL (2022)

Article Biochemistry & Molecular Biology

Single-Cell RNA Sequencing Reveals Molecular Features of Heterogeneity in the Murine Retinal Pigment Epithelium

Ravi S. Pandey, Mark P. Krebs, Mohan T. Bolisetty, Jeremy R. Charette, Jurgen K. Naggert, Paul Robson, Patsy M. Nishina, Gregory W. Carter

Summary: This study analyzed the transcriptome of mouse retinal pigment epithelium (RPE) using single-cell RNA sequencing, identifying six distinct cell populations and revealing cell heterogeneity within RPE. One cell population exhibited stem and/or progenitor characteristics. Analysis along a pseudotime axis showed a relative decrease in melanogenesis and SP gene expression and an increase in visual cycle gene expression during RPE maturation. Additional expression patterns were identified that may contribute to understanding RPE stem cell maintenance and cellular metabolic network evolution.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2022)

Correction Cell Biology

Single-cell analysis of endometriosis reveals a coordinated transcriptional programme driving immunotolerance and angiogenesis across eutopic and ectopic tissues (vol 24, pg 1306, 2022)

Yuliana Tan, William F. Flynn, Santhosh Sivajothi, Diane Luo, Suleyman B. Bozal, Monica Dave, Anthony A. Luciano, Paul Robson, Danielle E. Luciano, Elise T. Courtois

NATURE CELL BIOLOGY (2022)

Review Biology

Role of Senescent Cells in Cutaneous Wound Healing

Allison M. M. Andrade, Mingda Sun, Nathan S. S. Gasek, Geneva R. R. Hargis, Roshanak Sharafieh, Ming Xu

Summary: Cellular senescence plays a significant role in aging, tissue and wound repair, tumor biology, and development. It is an irreversible growth arrest induced by internal and external stress mechanisms. Senescent cell populations are diverse and finding a specific biomarker for this state is challenging. Despite its involvement in wound healing and tissue repair, the mechanisms by which senescent cells modulate regenerative processes remain unclear.

BIOLOGY-BASEL (2022)

Article Nutrition & Dietetics

Very Low and High Levels of Vitamin D Are Associated with Shorter Leukocyte Telomere Length in 148,321 UK Biobank Participants

Chia-Ling Kuo, Ben Kirk, Meiruo Xiang, Luke C. C. Pilling, George A. A. Kuchel, Richard Kremer, Gustavo Duque

Summary: This study examined the relationship between vitamin D levels and leukocyte telomere length (LTL) in older participants. It found that low or extremely low vitamin D levels were associated with shorter LTL, as well as high vitamin D levels. However, these associations may be influenced by unmeasured confounders.

NUTRIENTS (2023)

Article Cell Biology

NIH SenNet Consortium to map senescent cells throughout the human lifespan to understand physiological health

Patty J. Lee, Christopher C. Benz, Philip Blood, Katy Boerner, Judith Campisi, Feng Chen, Heike Daldrup-Link, Phil De Jager, Li Ding, Francesca E. Duncan, Oliver Eickelberg, Rong Fan, Toren Finkel, David Furman, Vesna Garovic, Nils Gehlenborg, Carolyn Glass, Indra Heckenbach, Ziv-Bar Joseph, Pragati Katiyar, So-Jin Kim, Melanie Koenigshoff, George A. Kuchel, Haesung Lee, Jun Hee Lee, Jian Ma, Qin Ma, Simon Melov, Kay Metis, Ana L. Mora, Nicolas Musi, Nicola Neretti, Joao F. Passos, Irfan Rahman, Juan Carlos Rivera-Mulia, Paul Robson, Mauricio Rojas, Ananda L. Roy, Morten Scheibye-Knudsen, Birgit Schilling, Pixu Shi, Jonathan C. Silverstein, Vidyani Suryadevara, Jichun Xie, Jinhua Wang, A. Ian Wong, Laura J. Niedernhofer, Siyuan (Steven) Wang, Hannah Anvari, Julia Balough, Christopher Benz, Joanna Bons, Boris Brenerman, William Evans, Akos Gerencser, Heather Gregory, Malene Hansen, Jamie Justice, Pankaj Kapahi, Natalia Murad, Amy O'Broin, Mary Ellen Pavone, Mark Powell, Gary Scott, Elisheva Shanes, Mahalakshmi Shankaran, Eric Verdin, Daniel Winer, Fei Wu, Andrew Adams, Philip D. Blood, Andreas Bueckle, Ivan Cao-Berg, Hao Chen, Michael Davis, Shane Filus, Yuhan Hao, Austin Hartman, Euxhen Hasanaj, Jesse Helfer, Bruce Herr, Ziv Bar Joseph, Gesmira Molla, Gloria Mou, Juan Puerto, Ellen M. Quardokus, Alexander J. Ropelewski, Matt Ruffalo, Rahul Satija, Melissa Schwenk, Robin Scibek, William Shirey, Max Sibilla, Joel Welling, Zhou Yuan, Richard Bonneau, Angela Christiano, Benjamin Izar, Vilas Menon, David M. Owens, Hemali Phatnani, Colin Smith, Yousin Suh, Andrew F. Teich, Valerie Bekker, Cliburn Chan, Elias Coutavas, Matthew G. Hartwig, Zhicheng Ji, Andrew B. Nixon, Zhixun Dou, Jayaraj Rajagopal, Nikolai Slavov, David Holmes, Diana Jurk, James L. Kirkland, Anthony Lagnado, Tamara Tchkonia, Kristin Abraham, Amanda Dibattista, Yih-Woei Fridell, T. Kevin Howcroft, Chamelli Jhappan, Viviana Perez Montes, Mercy Prabhudas, Haluk Resat, Veronica Taylor, Manoj Kumar, Francisco Cigarroa, Rachel Cohn, Tiffany M. Cortes, Elise Courtois, Jeffrey Chuang, Monica Dave, Sergii Domanskyi, Elizabeth Ann Lieser Enninga, Giray Naim Eryilmaz, Sara E. Espinoza, Jon Gelfond, James Kirkland, Chia-Ling Kuo, Julia S. Lehman, Cristina Aguayo-Mazzucato, Alexander Meves, Meenakshi Rani, Shane Sanders, Asa Thibodeau, Stefan G. Tullius, Duygu Ucar, Brian White, Qian Wu, Ming Xu, Seiji Yamaguchi, Naziheh Assarzadegan, Chun-Seok Cho, Irene Hwang, Yongha Hwang, Jingyue Xi, Oyedele A. Adeyi, Constantin F. Aliferis, Alessandro Bartolomucci, Xiao Dong, Mickayla J. DuFresne-To, Sayeed Ikramuddin, Steve G. Johnson, Andrew C. Nelson, Xavier S. Revelo, Claudia Trevilla-Garcia, John M. Sedivy, Elizabeth L. Thompson, Paul D. Robbins, Jinhua Wang, Katherine M. Aird, Jonathan K. Alder, Delphine Beaulieu, Marta Bueno, Jazmin Calyeca, Julian A. Chamucero-Millaris, Stephen Y. Chan, Dongjun Chung, Anthony Corbett, Vera Gorbunova, Kymberly M. Gowdy, Aditi Gurkar, Jeffrey C. Horowitz, Qianjiang Hu, Gagandeep Kaur, Timur O. Khaliullin, Robert Lafyatis, Serafina Lanna, Dongmei Li, Anjun Ma, Alison Morris, Thivanka M. Muthumalage, Victor Peters, Gloria S. Pryhuber, Brenda F. Reader, Lorena Rosas, John C. Sembrat, Sadiya Shaikh, Hangchuan Shi, Sean D. Stacey, Claudette St Croix, Cankun Wang, Qixin Wang, Andrew Watts, Liangcai Gu, Yiing Lin, Peter S. Rabinovitch, Mariya T. Sweetwyne, Maxim N. Artyomov, Samuel J. Ballentine, Milan G. Chheda, Sherri R. Davies, John F. DiPersio, Ryan C. Fields, James A. J. Fitzpatrick, Robert S. Fulton, Shin-ichiro Imai, Sanjay Jain, Tao Ju, Vladimir M. Kushnir, Daniel C. Link, Michael Ben Major, Stephen T. Oh, Daniel Rapp, Michael P. Rettig, Shelia A. Stewart, Deborah J. Veis, Kiran R. Vij, Michael C. Wendl, Matthew A. Wyczalkowski, Joseph E. Craft, Archibald Enninful, Negin Farzad, Peter Gershkovich, Stephanie Halene, Yuval Kluger, Jennifer VanOudenhove, Mina Xu, Junchen Yang, Mingyu Yang

Summary: Cells respond to stress by undergoing senescence, and the heterogeneity of senescent cells and their secretory phenotype need further characterization. The Cellular Senescence Network (SenNet) was established to create a map of senescent cells across the human lifespan and improve diagnostic and therapeutic approaches.

NATURE AGING (2022)

Meeting Abstract Oncology

IDENTIFYING REGULATORS OF GLIOMA CELL STATE DIVERSITY AND EVOLUTION VIA JOINT SINGLE NUCLEUS RNA AND CHROMATIN ACCESSIBILITY

Kevin Johnson, Kevin Anderson, Djamel Nehar-Belaid, Frederick Varn, Amit Gujar, Elise Courtois, Paul Robson, Hyo-Eun Moon, Anna Golebiewska, Sun Ha Paek, Simone Niclou, Roel Verhaak

NEURO-ONCOLOGY (2022)

Article Cell Biology

Transcriptional profiling of macrophages in situ in metastatic melanoma reveals localization-dependent phenotypes and function

Jan Martinek, Jianan Lin, Kyung In Kim, Victor G. Wang, Te-Chia Wu, Michael Chiorazzi, Hannah Boruchov, Ananya Gulati, Shamreethaa Seeniraj, Lili Sun, Florentina Marches, Paul Robson, Anthony Rongvaux, Richard A. Flavell, Joshy George, Jeffrey H. Chuang, Jacques Banchereau, Karolina Palucka

Summary: Modulating immune function at the tumor site could improve patient outcomes. This study shows that tumor infiltrating T cells are predominantly associated with CD14(+) monocytes/macrophages rather than melanoma cells in metastatic melanoma patients. Transcriptional analysis reveals that stromal CD14(+) cells have a distinct signature compared to CD14(+) cells within tumor nests and the included LY75 gene may serve as a potential biomarker for predicting prolonged survival in metastatic cutaneous melanoma and other cancers. Reprogramming stromal macrophages to acquire dendritic cell (DC) function could offer a therapeutic opportunity for metastatic cancers.

CELL REPORTS MEDICINE (2022)

Meeting Abstract Endocrinology & Metabolism

Senescence-like phenotype in monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM) plasma cells

Gabriel Alvares Borges, Angelo Guilatco, Sonya Royzenblat, Iyabode Ajayi, Claire Edwards, Ming Xu, Tamar Tchkonia, James Kirkland, Taxiarchis Kourelis, Matthew Drake, Megan Weivoda

JOURNAL OF BONE AND MINERAL RESEARCH (2022)

暂无数据