The candidate is a clinical endocrinologist dedicated to basic science research working under the mentorship of Dr. Janet Rubin for the past 2.5 years, initially as a T32 fellow and currently as junior faculty funded by UNC's prestigious BIRCWH award. In Dr. Rubin's laboratory, Dr. Styner acquired substantial expertise in the study of mechanisms by which mesenchymal stem cell (MSC) differentiation is regulated. Prior work in the Rubin lab revealed that mechanical repression of MSC adipogenesis involves decreased expression of PPARgamma; the candidate's own work led to the hypothesis that C/EBBeta), a transcription factor expressed early in adipogenesis, might be critically involved in mechanical repression of adipogenesis through regulation of PPARgamma. This hypothesis will be tested in SA1, where C/EBBeta's role in MSC differentiation will be analyzed using substrate stretch to deliver mechanical input in vitro and using wheel based running exercise in mice in vivo. C/EBBeta) and potential regulators will be varied using molecular techniques during the mechanical/exercise input. In SA2 the candidate proposes that mechanical-exercise induced down regulation of C/EBBeta) will protect against MSC endoplasmic reticulum (ER) stress. Preliminary data show that MSCs subject to mechanical strain are resistant to the pro-apoptotic effects of ER stress, preventing adipogenesis and preserving MSC potential. Experiments will characterize C/EBBeta)'s role in ER stress in vitro and in vivo and the ability exercise to protect through limiting C/EBBeta) expression. An effect of exercise to regulate both adipogenesis and ER stress via C/EBBeta) would represent novel mechanisms for salutary effects of exercise. The candidate's short-term career goals include 1) building on her technical skills in molecular biology and acquiring new skills in microscopy and the conduct of animal research including the use of in-vivo exercise models, 2) increasing her strategy and data analysis skills, as well as skills in running a laboratory 3) expanding her knowledge in the field of ER stress and 4) developing her skills in writing and grantsmanship. The candidate's long-term-career goal is to become an independent investigator with expertise in the effects of exercise on fat and skeletal biology with an emphasis on understanding basic mechanisms affected by exercise (MSC differentiation and ER stress). The candidate's primary mentor, Dr. Janet Rubin, is a physician scientist with a record of training young investigators and with an international reputation in the field of mechanical effects in skeletal biology. The co-mentor, Dr. Cam Patterson, has an excellent record of training investigators and will provide Dr. Styner with content area expertise in the field of ER stress. The research environment will provide a productive, supportive and collegial background to pursue the proposed research and to develop an independent career where the candidate intends to bring knowledge of exercise effects on cells to the treatment of chronic diseases such as osteoporosis, frailty and obesity.

Public Health Relevance

Exercise-based therapies increase bone strength and offer non-pharmacologic strategies to combat osteoporosis, a condition which carries significant morbidity and mortality in our aging population. The goal of this proposal is to characterize the mechanisms by which exercise/ mechanical signals repress mesenchymal stem cell (MSC) adipogenesis, thus improving MSC potential for osteogenic differentiation and resistance to cellular stress.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Clinical Investigator Award (CIA) (K08)
Project #
4K08AR062097-05
Application #
9079356
Study Section
Arthritis and Musculoskeletal and Skin Diseases Special Grants Review Committee (AMS)
Program Officer
Alekel, D Lee
Project Start
2012-04-01
Project End
2017-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
5
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Uzer, Gunes; Bas, Guniz; Sen, Buer et al. (2018) Sun-mediated mechanical LINC between nucleus and cytoskeleton regulates ?catenin nuclear access. J Biomech 74:32-40
Stieglitz, Heather M; Korpi-Steiner, Nichole; Katzman, Brooke et al. (2018) Suspected Testosterone-Producing Tumor in a Patient Taking Biotin Supplements. J Endocr Soc 2:563-569
Styner, Maya; Korpi-Steiner, Nichole (2018) Commentary. Clin Chem 64:51-52
Thompson, William R; Yen, Sherwin S; Uzer, Gunes et al. (2018) LARG GEF and ARHGAP18 orchestrate RhoA activity to control mesenchymal stem cell lineage. Bone 107:172-180
Rubin, Janet; Styner, Maya; Uzer, Gunes (2018) Physical Signals May Affect Mesenchymal Stem Cell Differentiation via Epigenetic Controls. Exerc Sport Sci Rev 46:42-47
Styner, Maya; Pagnotti, Gabriel M; McGrath, Cody et al. (2017) Exercise Decreases Marrow Adipose Tissue Through ß-Oxidation in Obese Running Mice. J Bone Miner Res 32:1692-1702
Sen, Buer; Uzer, Gunes; Samsonraj, Rebekah M et al. (2017) Intranuclear Actin Structure Modulates Mesenchymal Stem Cell Differentiation. Stem Cells 35:1624-1635
Pagnotti, Gabriel M; Styner, Maya (2016) Exercise Regulation of Marrow Adipose Tissue. Front Endocrinol (Lausanne) 7:94
Morton, Tiffany L; Galior, Kornelia; McGrath, Cody et al. (2016) Exercise Increases and Browns Muscle Lipid in High-Fat Diet-Fed Mice. Front Endocrinol (Lausanne) 7:80
Styner, Maya; Pagnotti, Gabriel M; Galior, Kornelia et al. (2015) Exercise Regulation of Marrow Fat in the Setting of PPAR? Agonist Treatment in Female C57BL/6 Mice. Endocrinology 156:2753-61

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