Literature DB >> 34463901

Einstein-Nathan Shock Center: translating the hallmarks of aging to extend human health span.

Ana Maria Cuervo1,2,3,4, Derek M Huffman1,3,4,5, Jan Vijg3,4,6, Sofiya Milman1,3,4, Rajat Singh1,2,3,4, Nir Barzilai7,8,9,10.   

Abstract

The overarching mission of the Einstein-Nathan Shock Center (E-NSC) is to make scientific discoveries in geroscience, leveraging on the expertise in our center in 6 out of the 7 pillars of aging, and to translate their effects towards drug discovery. The relevance of this basic biology of aging discoveries to humans will be confirmed through the unique gero-human resource at E-NSC. This is achieved through services provided by E-NSC, connectivity among its members, attracting worldwide investigators, and providing them with the opportunities to become future leaders. The two central components of the E-NSC are (a) cutting-edge research programs and (b) unique E-NSC research support cores. E-NSC scientists lead NIH-supported cutting-edge research programs that integrate key hallmarks of aging including proteostasis/autophagy, metabolism/inflammaging, genetic/epigenetics, stem cells/regeneration, and translational aging/longevity. Since the inception of the E-NSC, the well-integrated, collaborative, and innovative nature of the multiple supporting state-of-the-art E-NSC research cores form the bedrock of research success at the E-NSC. The three state-of-the-art E-NSC research cores, (i) Proteostasis of Aging Core (PAC), (ii) the Health Span Core (HSC), and (iii) the Human Multi-Omics Core (HMOC), have allowed impressive expansion of translational biological research programs. Expansion was facilitated through the wealth of data coming from genomics/proteomics and metabolomic analysis on human longevity studies, due to access to a variety of biological samples from elderly subjects in clinical trials with aging-targeting drugs, and new drug design services via the PAC to target the hallmarks of aging.
© 2021. American Aging Association.

Entities:  

Keywords:  Autophagy; Genomics; Health span; Metabolism; Parabiosis; Proteomics; Proteostasis

Mesh:

Year:  2021        PMID: 34463901      PMCID: PMC8599554          DOI: 10.1007/s11357-021-00428-9

Source DB:  PubMed          Journal:  Geroscience        ISSN: 2509-2723            Impact factor:   7.713


  79 in total

1.  A role for NPY overexpression in the dorsomedial hypothalamus in hyperphagia and obesity of OLETF rats.

Authors:  S Bi; E E Ladenheim; G J Schwartz; T H Moran
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2001-07       Impact factor: 3.619

2.  Age-related changes in body composition are associated with hepatic insulin resistance in conscious rats.

Authors:  N Barzilai; L Rossetti
Journal:  Am J Physiol       Date:  1996-06

3.  Leptin selectively decreases visceral adiposity and enhances insulin action.

Authors:  N Barzilai; J Wang; D Massilon; P Vuguin; M Hawkins; L Rossetti
Journal:  J Clin Invest       Date:  1997-12-15       Impact factor: 14.808

4.  Intracerebroventricular CART peptide reduces food intake and alters motor behavior at a hindbrain site.

Authors:  S Aja; S Sahandy; E E Ladenheim; G J Schwartz; T H Moran
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2001-12       Impact factor: 3.619

5.  Caloric restriction reverses hepatic insulin resistance in aging rats by decreasing visceral fat.

Authors:  N Barzilai; S Banerjee; M Hawkins; W Chen; L Rossetti
Journal:  J Clin Invest       Date:  1998-04-01       Impact factor: 14.808

6.  Unique lipoprotein phenotype and genotype associated with exceptional longevity.

Authors:  Nir Barzilai; Gil Atzmon; Clyde Schechter; Ernst J Schaefer; Adrienne L Cupples; Richard Lipton; Suzanne Cheng; Alan R Shuldiner
Journal:  JAMA       Date:  2003-10-15       Impact factor: 56.272

7.  Mediobasal hypothalamic p70 S6 kinase 1 modulates the control of energy homeostasis.

Authors:  Clémence Blouet; Hiraku Ono; Gary J Schwartz
Journal:  Cell Metab       Date:  2008-12       Impact factor: 27.287

8.  Relationship between changes in body composition and insulin responsiveness in models of the aging rat.

Authors:  N Barzilai; L Rossetti
Journal:  Am J Physiol       Date:  1995-09

9.  Increased Wnt signaling during aging alters muscle stem cell fate and increases fibrosis.

Authors:  Andrew S Brack; Michael J Conboy; Sudeep Roy; Mark Lee; Calvin J Kuo; Charles Keller; Thomas A Rando
Journal:  Science       Date:  2007-08-10       Impact factor: 47.728

10.  Disulfiram Treatment Normalizes Body Weight in Obese Mice.

Authors:  Michel Bernier; Sarah J Mitchell; Devin Wahl; Antonio Diaz; Abhishek Singh; Wonhyo Seo; Mingy Wang; Ahmed Ali; Tamzin Kaiser; Nathan L Price; Miguel A Aon; Eun-Young Kim; Michael A Petr; Huan Cai; Alessa Warren; Clara Di Germanio; Andrea Di Francesco; Ken Fishbein; Vince Guiterrez; Dylan Harney; Yen Chin Koay; John Mach; Ignacio Navas Enamorado; Tamara Pulpitel; Yushi Wang; Jing Zhang; Li Zhang; Richard G Spencer; Kevin G Becker; Josephine M Egan; Edward G Lakatta; John O'Sullivan; Mark Larance; David G LeCouteur; Victoria C Cogger; Bin Gao; Carlos Fernandez-Hernando; Ana Maria Cuervo; Rafael de Cabo
Journal:  Cell Metab       Date:  2020-05-14       Impact factor: 27.287

View more
  1 in total

1.  Old blood from heterochronic parabionts accelerates vascular aging in young mice: transcriptomic signature of pathologic smooth muscle remodeling.

Authors:  Tamas Kiss; Ádám Nyúl-Tóth; Rafal Gulej; Stefano Tarantini; Tamas Csipo; Derek M Huffman; Anna Csiszar; Zoltan Ungvari; Peter Mukli; Anna Ungvari; Priya Balasubramanian; Andriy Yabluchanskiy; Zoltan Benyo; Shannon M Conley; Jonathan D Wren; Lori Garman
Journal:  Geroscience       Date:  2022-02-05       Impact factor: 7.581

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.