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Mechanisms for Cellular Aging

The mechanisms of cellular aging is a major area of research at the Institute for Geroscience at Albert Einstein College of Medicine. We study how malfunctioning cellular processes contribute to aging, with a focus on three major lines of research.

Functional Consequences of Impaired Autophagy in Aging

Impairment in autophagy, a major cellular cleaning and recycling process, may be the basis for functional deterioration and inability to respond to immunological challenges and stress in aging organisms. We study the:

  • impact of changes with age in autophagic pathways on the cellular and organism response to stress.
  • contribution of autophagy malfunction in aging to immunosenescence (the age-related deterioration of the immune system).
  • contribution of the age-dependent decline in autophagy to the metabolic syndrome of aging.

Senescence in Aging

Accumulation of senescent cells—damaged cells that stop multiplying but don’t die off when they should—is a major contributor to a wide range of age-related diseases, and reducing the number of senescent cells has been shown to lessen disease. The selective killing of senescent cells (senolysis) has become a major therapeutic goal to attenuate age-related organ dysfunction. This collaborative program includes the following studies:

  • molecular determinants of the cell death/senescence decision
  • role of autophagy malfunctioning in persistent senescence in aging
  • therapeutic targeting of unique vulnerabilities in old senescent cells 

Stem Cell Exhaustion

Stem cells are central to tissue repair and regeneration, but their function declines with age due to intrinsic factors such as DNA damage, epigenetic drift, metabolic dysfunction, and proteostasis failure, as well as extrinsic changes in the niche and systemic environment, including inflammation and senescence. This loss of regenerative capacity underlies frailty and many age-related diseases. Understanding how aging alters the balance between stem cell quiescence and activation, and exploring strategies such as metabolic reprogramming, niche modulation, senescent cell clearance, or partial reprogramming, holds promise for restoring stem cell function and extending healthspan. Research in this area at the institute includes the following:

  • intrinsic drivers of stem cell aging
  • impact of niche and systemic environment on stem cell function
  • rejuvenation and therapeutic modulation of aging stem cells

Faculty

Director

Ana Maria Cuervo, M.D., Ph.D.

Robert and Renée Belfer Chair for the Study of Neurodegenerative Diseases

Investigators

Matthew K. Abramowitz, MD, MS

Professor, Department of Medicine

Esperanza Arias-Perez, Ph.D.

Associate Professor, Department of Medicine

Teresa V. Bowman, Ph.D.

Chair, Department of Developmental & Molecular Biology

Anne R. Bresnick, Ph.D.

Associate Dean for Postdoctoral Affairs

Nikolaos G. Frangogiannis, M.D.

Edmond J. Safra/Republic National Bank of New York Chair in Cardiovascular Medicine

Evripidis Gavathiotis, Ph.D.

Co-Leader, Montefiore Einstein Comprehensive Cancer Center, Cancer Therapeutics Program

J. Tiago Goncalves, Ph.D.

Associate Professor, Dominick P. Purpura Department of Neuroscience

Susmita Kaushik, Ph.D.

Research Associate Professor, Department of Developmental & Molecular Biology

Richard N. Kitsis, MD

Attending Cardiologist, Montefiore

Hayley M. McDaid, Ph.D.

Associate Professor, Department of Oncology

Satish K. Nandakumar, M.B.,B.S., Ph.D.

Assistant Professor, Department of Cell Biology

Aditi Shastri, MD

Assistant Director, Translational Research

Simone Sidoli, Ph.D.

Associate Professor, Department of Biochemistry

Britta Will, Ph.D.

Co-Leader, Montefiore Einstein Comprehensive Cancer Center, Stem Cell & Cancer Biology Program