Chelsea L Hepler
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About
Dr. Hepler earned her PhD in Integrative Biology in the laboratory of Rana Gupta at UT Southwestern, followed by her postdoctoral fellowship in the laboratory of Joe Bass at Northwestern University. In 2024, Dr. Hepler joined the University of Michigan as an assistant professor in the Molecular & Integrative Physiology department and the Caswell Diabetes Institute. Her goal is to uncover the mechanisms through which the circadian clock regulates metabolism and physiology, and how circadian disruption leads to metabolic disease.
Links
Hepler Lab
Qualifications
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Postdoctoral FellowshipNorthwestern University, Evanston, United States
2018 - 2024
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PhDUT Southwestern Medical Center, Dallas, United States
2014 - 2018
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MSUniversity of Arizona, Tucson, United States
2012 - 2014
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BSUniversity of Arizona, Tucson, United States
2008 - 2011
Center Memberships
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Center MemberCaswell Diabetes Institute
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Center MemberCenter for Cell Plasticity and Organ Design
Research Overview
Disruption of circadian rhythms through shiftwork, sleep loss, and mistimed eating leads to an increased risk of diabetes and obesity. Conversely, aligning mealtime with circadian rhythms improves glycemic control and reduces adiposity, in part through mechanisms involving adipose tissue remodeling. Adipose tissue demonstrates remarkable plasticity, adapting its size, cellular composition, and metabolism in response to various external cues, including overnutrition and time-restricted eating. My lab is dedicated to understanding the physiologic regulation of energy balance and the pathologic expansion of adipose tissue during obesity. Our goal is to uncover how the circadian clock regulates adipose tissue metabolism and physiology in response to shifting environmental signals, and to understand how circadian disruption leads to metabolic diseases.
Recent Publications
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Moy BM, Rodrigues T, Komanduri S, Aadam AA, Keswani RN, Sinha J, Hepler C, Xia JY. Gastrointestinal Endoscopy, 2026 May 6; 103 (5): s-2127-s-2128Journal Article648 NOVEL BILE-BASED MICROBIOME SIGNATURES FOR PREDICTING POST-ERCP PANCREATITIS
DOI:10.1016/s0016-5107(26)04986-2 -
Moy BM, Rodrigues T, Komanduri S, Aadam AA, Keswani RN, Sinha J, Hepler C, Xia JY. Gastroenterology, 2026 May 7; 170 (6): s-2127-s-2128Journal Article648 NOVEL BILE-BASED MICROBIOME SIGNATURES FOR PREDICTING POST-ERCP PANCREATITIS
DOI:10.1016/s0016-5085(26)05055-9 -
Xia JY, Rodrigues T, Komanduri S, Keswani RN, Sinha J, Hepler C, Aadam AA. Gastroenterology, 2026 May 6; 170 (6): s-22-s-23Journal Article791 A NOVEL BILE BIOMARKER PANEL ENHANCES DETECTION OF MALIGNANT STRICTURES DURING ERCP
DOI:10.1016/s0016-5085(26)00410-5 -
Xia JY, Rodrigues T, Komanduri S, Keswani RN, Sinha J, Hepler C, Aadam AA. Gastrointestinal Endoscopy, 2026 May 6; 103 (5): s-22-s-23Journal Article791 A NOVEL BILE BIOMARKER PANEL ENHANCES DETECTION OF MALIGNANT STRICTURES DURING ERCP
DOI:10.1016/s0016-5107(26)00341-x -
Hepler C, Waldeck NJ, Weidemann BJ, Marcheva B, Chen YJ, Hecker J, Zhu Z, Nozawa R, Mastroni JV, Thorne AK, Reczek CR, Cedernaes J, Ramsey KM, Peek CB, Barish GD, Chandel NS, Bass J. Nature Metabolism, 2026 Jan 1;Journal ArticleAdipocyte NADH dehydrogenase reverses circadian and diet-induced metabolic syndrome
DOI:10.1038/s42255-026-01464-5 PMID: 41708974 -
Dumont KD, Seradj SH, Wang Y, Liu S, Cervenka I, Wu C, Jannig PR, Porsmyr-Palmertz M, Baiges-Gaya G, Huang X, Nihlen C, Dias JM, Skiotyte SS, Prastholm SM, Quinn M, Lundberg JO, Teixeira AI, Rosenzweig A, Wu J, Ye L, Ruas JL. Cell reports, 2025 Apr 7;Journal ArticleSensory neuron-derived CGRPalpha controls white adipocyte differentiation and tissue plasticity
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Hepler C, Waldeck NJ, Weidemann BJ, Marcheva B, Chen Y-J, Hecker J, Zhu Z, Nozawa R, Mastroni JV, Thorne AK, Reczek CR, Cedernaes J, Ramsey KM, Peek CB, Barish GD, Chandel NS, Bass J. 2025 Oct 23;PreprintNADH dehydrogenase reverses dietary and clock metabolic syndrome.
DOI:10.1101/2025.10.22.684030 PMID: 41279878 -
Xia JY, Komanduri S, Keswani RN, Rodrigues TR, Sinha J, Rengarajan A, Tran P, Hepler C, Prindle A, Aadam AA. Hepatology Communications, 2025 Sep 1; 9 (9):Journal ArticleIntegrating multi-omics in bile for biomarker discovery in cholangiocarcinoma
DOI:10.1097/HC9.0000000000000786 PMID: 40857390
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