Paul M. Titchenell, Ph.D.

faculty photo
Assistant Professor of Physiology
Director, Social Media and Scientific Outreach, Institute for Diabetes, Obesity and Metabolism, University of Pennsylvania
Member, Center for Molecular Studies in Digestive and Liver Disease, University of Pennsylvania
Member, Institute for Diabetes, Obesity & Metabolism, University of Pennsylvania
Member, Institute for Translational Medicine and Therapeutics, University of Pennsylvania
Member, Pennsylvania Muscle Institute , University of Pennsylvania
Member, Cardiovascular Institute, University of Pennsylvania
Member, Penn Center for Musculoskeletal Disorders, University of Pennsylvania
Assistant Director, Trainee Recruitment , Inclusivity, Diversity, Equity, and Learner (IDEAL) Research, University of Pennsylvania
Co-Director, Academic Enrichment Program, Diabetes Research Center, University of Pennsylvania
Co-Director, SUIP, Inclusivity, Diversity, Equity, and Learner (IDEAL) Research, University of Pennsylvania
Co-lead, Liver Biology Group, Center for Molecular Studies in Digestive and Liver Disease, University of Pennsylvania
Department: Physiology

Contact information
Institute for Diabetes, Obesity, and Metabolism
Smilow Center for Translational Research
3400 Civic Center Blvd, Building 421
Room: 12-104
Philadelphia, PA 19104
Office: 215-573-1872
Lab: 215-573-1875
Education:
B.S. (Biochemistry and Molecular Biology)
Dickinson College, 2008.
Ph.D. (Physiology)
Pennsylvania State University, 2013.
Permanent link
 
> Perelman School of Medicine   > Faculty   > Details

Description of Research Expertise

Research Interests:
Molecular mechanisms of insulin signaling, insulin resistance, and metabolism

Keywords:
metabolism, insulin, diabetes, obesity, AKT, mTORC1

Research Details:
My research interests are focused on the regulation of metabolism by hormones and nutrients, with a particular emphasis on a master regulator of organismal anabolic metabolism, insulin. Alterations in insulin action underlie metabolic disease and lead to the development of deadly vascular and neuronal complications. Through the use of various techniques encompassing molecular biology, biochemistry, metabolomics, genome-wide transcriptional techniques and whole-animal physiology, the long-term goals of my research program are to decipher the underlying mechanisms driving metabolic deregulation during disease and identify new therapies that improve metabolic control.

Current Lab personnel:
Matthew Gavin (Research Specialist)
Natasha Jaiswal Ph.D. (Postdoctoral Researcher)
Jaclyn Welles Ph.D. (Postdoctoral Researcher)
Kahea Uehara (PhD student, BMB graduate group)
Dominic Santoleri (PhD student, BMB graduate group)
Anna Garcia Whitlock M.D. (PhD student, CAMB graduate group)
Megan Stefkovich, (PhD student, CAMB graduate group)
Talia Coopersmith (Penn undergraduate-PURM)
Olivia Ong (Penn undergraduate)

Selected Publications

Sostre-Colón J, Gavin MJ, Santoleri D, Titchenell PM.: Acute Deletion of the FOXO1-dependent Hepatokine FGF21 Does not Alter Basal Glucose Homeostasis or Lipolysis in Mice. Endocrinology 163: bqac035, May 2022.

Uehara K, Sostre-Colón J, Gavin M, Santoleri D, Leonard KA, Jacobs RL, Titchenell PM.: Activation of Liver mTORC1 Protects Against NASH via Dual Regulation of VLDL-TAG Secretion and De Novo Lipogenesis. Cell Mol Gastroenterol Hepatol 13: 1625-1647, Feb 2022.

Gosis BS, Wada S, Thorsheim C, Li K, Jung S, Rhoades JH, Yang Y, Brandimarto J, Li L, Uehara K, Jang C, Lanza M, Sanford NB, Bornstein MR, Jeong S, Titchenell PM, Biddinger SB, Arany Z.: Inhibition of nonalcoholic fatty liver disease in mice by selective inhibition of mTORC1. Science 376: eabf8271, Apr 2022.

Sostre-Colón J, Uehara K, Garcia Whitlock AE, Gavin MJ, Ishibashi J, Potthoff MJ, Seale P, Titchenell PM.: Hepatic AKT orchestrates adipose tissue thermogenesis via FGF21-dependent and -independent mechanisms. Cell Rep 35: 109128, May 2021.

Quinn WJ 3rd, Wan M, Shewale SV, Gelfer R, Rader DJ, Birnbaum MJ, Titchenell PM.: mTORC1 stimulates phosphatidylcholine synthesis to promote triglyceride secretion. J Clin Invest 127: 4207-4215, Nov 2017.

Titchenell PM, Quinn WJ, Lu M, Chu Q, Lu W, Li C, Chen H, Monks BR, Chen J, Rabinowitz JD, Birnbaum MJ.: Direct Hepatocyte Insulin Signaling Is Required for Lipogenesis but Is Dispensable for the Suppression of Glucose Production. Cell Metab 23: 1154-1166, Jun 2016.

Titchenell PM, Chu Q, Monks BR, Birnbaum MJ.: Hepatic insulin signalling is dispensable for suppression of glucose output by insulin in vivo. Nat Commun 6: 7078, May 2015.

back to top
Last updated: 09/23/2022
The Trustees of the University of Pennsylvania