M
Michael B. Stout
Researcher at University of Oklahoma Health Sciences Center
Publications - 63
Citations - 4778
Michael B. Stout is an academic researcher from University of Oklahoma Health Sciences Center. The author has contributed to research in topics: Medicine & Adipose tissue. The author has an hindex of 20, co-authored 45 publications receiving 3221 citations. Previous affiliations of Michael B. Stout include Mayo Clinic.
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Journal ArticleDOI
The Achilles’ heel of senescent cells: from transcriptome to senolytic drugs
Yi-Yi Zhu,Tamara Tchkonia,Tamar Pirtskhalava,Adam C. Gower,Husheng Ding,Nino Giorgadze,Allyson K. Palmer,Yuji Ikeno,Yuji Ikeno,Gene B. Hubbard,Gene B. Hubbard,Marc E. Lenburg,Steven P. O'Hara,Nicholas F. LaRusso,Jordan D. Miller,Carolyn M Roos,Grace C Verzosa,Nathan K. LeBrasseur,Jonathan D. Wren,Joshua N. Farr,Sundeep Khosla,Michael B. Stout,Sara J. McGowan,Heike Fuhrmann-Stroissnigg,Aditi U. Gurkar,Jing-jing Zhao,Debora Colangelo,Akaitz Dorronsoro,Yuan Yuan Ling,Amira S. Barghouthy,Diana C. Navarro,Tokio Sano,Paul D. Robbins,Laura J. Niedernhofer,James L. Kirkland +34 more
TL;DR: The results demonstrate the feasibility of selectively ablating senescent cells and the efficacy of senolytics for alleviating symptoms of frailty and extending healthspan.
Journal ArticleDOI
Identification of a novel senolytic agent, navitoclax, targeting the Bcl-2 family of anti-apoptotic factors.
Yi Zhu,Tamara Tchkonia,Heike Fuhrmann-Stroissnigg,Haiming Dai,Yuanyuan Y. Ling,Michael B. Stout,Tamar Pirtskhalava,Nino Giorgadze,Kurt O. Johnson,Cory B. Giles,Jonathan D. Wren,Laura J. Niedernhofer,Paul D. Robbins,James L. Kirkland +13 more
TL;DR: The hypothesis‐driven, bioinformatics‐based approach used to discover that dasatinib (D) and quercetin (Q) are senolytic can be extended to increase the repertoire ofsenolytic drugs, including additional cell type‐specific senolytics agents.
Journal ArticleDOI
JAK inhibition alleviates the cellular senescence-associated secretory phenotype and frailty in old age
Ming Xu,Tamara Tchkonia,Husheng Ding,Mikolaj Ogrodnik,Mikolaj Ogrodnik,Ellen R. Lubbers,Tamar Pirtskhalava,Thomas A. White,Kurt O. Johnson,Michael B. Stout,Vojtech Mezera,Nino Giorgadze,Michael D. Jensen,Nathan K. LeBrasseur,James L. Kirkland +14 more
TL;DR: It is found that senescent fat progenitor cells accumulate in adipose tissue with aging and acquire a senescence-associated secretory phenotype (SASP), with increased production of proinflammatory cytokines compared with nonsenescent cells.
Journal ArticleDOI
Targeting senescent cells enhances adipogenesis and metabolic function in old age
Ming Xu,Allyson K. Palmer,Husheng Ding,Megan M. Weivoda,Tamar Pirtskhalava,Thomas A. White,Anna Sepe,Kurt O. Johnson,Michael B. Stout,Nino Giorgadze,Michael D. Jensen,Nathan K. LeBrasseur,Tamar Tchkonia,James L. Kirkland +13 more
TL;DR: This study indicates targeting senescent cells or their products may alleviate age-related dysfunction of progenitors, adipose tissue, and metabolism.
Journal ArticleDOI
Targeting senescent cells alleviates obesity‐induced metabolic dysfunction
Allyson K. Palmer,Ming Xu,Ming Xu,Yi Zhu,Tamar Pirtskhalava,Megan M. Weivoda,Christine M Hachfeld,Larissa G.P. Langhi Prata,Theo H. van Dijk,Esther Verkade,Grace Casaclang-Verzosa,Kurt O. Johnson,Hajrunisa Cubro,Ewald J. Doornebal,Mikolaj Ogrodnik,Mikolaj Ogrodnik,Diana Jurk,Diana Jurk,Michael D. Jensen,Eduardo N. Chini,Jordan D. Miller,Aleksey V. Matveyenko,Michael B. Stout,Marissa J. Schafer,Thomas A. White,La Tonya J. Hickson,Marco Demaria,Marco Demaria,Vesna D. Garovic,Joseph P. Grande,Edgar A. Arriaga,Folkert Kuipers,Thomas von Zglinicki,Nathan K. LeBrasseur,Judith Campisi,Tamar Tchkonia,James L. Kirkland +36 more
TL;DR: It is shown that reducing senescent cell burden in obese mice, either by activating drug‐inducible “suicide” genes driven by the p16Ink4a promoter or by treatment with senolytic agents, alleviates metabolic and adipose tissue dysfunction and that emerging senolytics agents hold promise for treating obesity‐related metabolic dysfunction and its complications.