This is the first competitive renewal for the transformative Einstein Nathan Shock Center (E-NSC). During the first grant period, funding exclusively for biology of aging tripled in size, and was accompanied by an impressive publications record E-NSC members as exemplified in 124 papers and reviews in Nature and Science-journals, a staggering average of approximately 6 collaborative papers (with other E-NSC members) per E-NSC investigator and the proactive recruitment and 'conversion' of 25 members to the E-NSC who were not members for the first submission. Our membership now includes internal (52) and external (11) members as well as support for a 'mini-NSC' with Brown University (5) investigators. Other resources are also highly important for E-NSC success, including large aging Program Projects, an ongoing NIH-funded Einstein Aging (T32) training grant, a complementary graduate course on the Biology of Aging, and the Glenn Center for Biology of Human Aging at Einstein. Activities of the E-NSC were leveraged by supplemental Institutional funding; the Center awarded 18 pilot and feasibility grants, with good outcomes. The three Research Resource Cores provided services to over 150 investigators, offering state-of the art services with dependable quality control at an affordable price.
The aims of the E-NSC are: 1) To enhance and expand ongoing basic biology of aging research by providing state of the art and unique new technologies for our three Research Resource Cores: a) Proteostasis of Aging Core (PAC, Dr. Ana Maria Cuervo); b) Chronobiosis, Energetics/Metabolism of Aging Core (CEAC, Drs. Nir Barzilai and Derek Huffman); c) Advanced Genomics of Aging Core (AGAC, Dr. Jan Vijg). 2) The Administrative Core (Dr. Barzilai) implements and administers enrichment activities through a lecture series, mini-retreats and attendance at NSC national meetings, and will continue to develop potential regional and/or national resources. 3) To provide support and a suitable environment for new investigators in biology of aging research through a Research Development Core (Dr. Yousin Suh) that will provide P&F awards to deserving investigators.

Public Health Relevance

Research centers of excellence have emerged to stimulate the investigator intellectual environment for specific fields of research and to provide technology that is not practicable the individual scientist. With support for 3 research resource cores, pilot& feasibility awards, a designated mentor system program enrichment and a yearly mini-retreat, this Einstein Nathan Shock Center will continue to transform the field with the goal to delay human aging and its associated diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
5P30AG038072-08
Application #
9110109
Study Section
Special Emphasis Panel (ZAG1-ZIJ-2 (M1))
Program Officer
Sierra, Felipe
Project Start
2010-08-15
Project End
2020-06-30
Budget Start
2016-08-15
Budget End
2017-06-30
Support Year
8
Fiscal Year
2016
Total Cost
$525,152
Indirect Cost
$211,681
Name
Albert Einstein College of Medicine, Inc
Department
Type
DUNS #
079783367
City
Bronx
State
NY
Country
United States
Zip Code
10461
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Walters, Ryan O; Arias, Esperanza; Diaz, Antonio et al. (2018) Sarcosine Is Uniquely Modulated by Aging and Dietary Restriction in Rodents and Humans. Cell Rep 25:663-676.e6
Mocholi, Enric; Dowling, Samuel D; Botbol, Yair et al. (2018) Autophagy Is a Tolerance-Avoidance Mechanism that Modulates TCR-Mediated Signaling and Cell Metabolism to Prevent Induction of T Cell Anergy. Cell Rep 24:1136-1150
Guan, Fangxia; Tabrizian, Tahmineh; Novaj, Ardijana et al. (2018) Dietary Walnuts Protect Against Obesity-Driven Intestinal Stem Cell Decline and Tumorigenesis. Front Nutr 5:37
Tekirdag, Kumsal; Cuervo, Ana Maria (2018) Chaperone-mediated autophagy and endosomal microautophagy: Joint by a chaperone. J Biol Chem 293:5414-5424
Theofilas, Panos; Ehrenberg, Alexander J; Nguy, Austin et al. (2018) Probing the correlation of neuronal loss, neurofibrillary tangles, and cell death markers across the Alzheimer's disease Braak stages: a quantitative study in humans. Neurobiol Aging 61:1-12
Choi, Jiahn; Rakhilin, Nikolai; Gadamsetty, Poornima et al. (2018) Intestinal crypts recover rapidly from focal damage with coordinated motion of stem cells that is impaired by aging. Sci Rep 8:10989
Sathyan, Sanish; Barzilai, Nir; Atzmon, Gil et al. (2018) Genetic Insights Into Frailty: Association of 9p21-23 Locus With Frailty. Front Med (Lausanne) 5:105
Amengual, Jaume; Guo, Liang; Strong, Alanna et al. (2018) Autophagy Is Required for Sortilin-Mediated Degradation of Apolipoprotein B100. Circ Res 122:568-582
Mao, Kai; Quipildor, Gabriela Farias; Tabrizian, Tahmineh et al. (2018) Late-life targeting of the IGF-1 receptor improves healthspan and lifespan in female mice. Nat Commun 9:2394

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