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Keren Hilgendorf

Assistant Professor of BiochemistryKeren I Hilgendorf

B.S. University of Texas at Austin

Ph.D. Massachusetts Institute of Technology

Research

Publications

keren.hilgendorf@biochem.utah.edu

Keren Hilgendorf's Lab Page

Keren Hilgendorf's PubMed Literature Search

Molecular Biology Program

Signal transduction pathways, differentiation, stem cells, white adipose tissue, primary cilium

Research 

Overview:

Tissue maintenance, expansion, and repair require stem and progenitor cells to respond to a wide range of physiological signals. Our lab explores what these signals are, how they regulate stem cell differentiation a molecular level, and how alterations drive pathogenesis. One major focus of the lab is to study the molecular mechanisms regulating adipogenesis. To do this, we use a combination of animal models and cell culture techniques. We are particularly interested in understanding how the primary cilium, an antenna-like signaling organelle, senses and organizes signal transduction pathways to regulate stem cell fate. 

Adipogenesis

We have a strong interest in studying fat differentiation and white adipose tissue expansion. The prevalence of obesity, defined as excess white adipose tissue, has reached pandemic levels and its comorbidities, including diabetes and cancer, pose a significant challenge to public health. Adipose tissue expands by generating more fat cells as well as storing more lipids in existing fat cells. The relative balance between these two mechanisms has a profound effect on metabolic health: Larger fat cells are associated with insulin resistance and inflammation leading to diabetes, while white adipose tissue containing smaller fat cells, even if greater in number, is considered metabolically healthy. We want to identify the physiological and endocrine signals that regulate how white adipose tissue expands.

Primary Cilium

One major focus in the lab is the primary cilium, a central sensory organelle of the cell. Mesenchymal stem and progenitor cells, which give rise to fat, muscle, bone, and cartilage, are all ciliated. We and others have shown that loss of ciliation on mesenchymal progenitor cells impairs tissue homeostasis, regeneration, and expansion. Human genetic mutations leading to dysfunctional cilia (ciliopathies) can manifest obesity, diabetes, hypotonia, and skeletal dysplasia.

We want to understand how primary cilia on stem and progenitor cells regulate differentiation, including which physiological signals they sense, how these get communicated to the transcriptional machinery of the cell, how subcellular localization to the primary cilium regulates and enables signaling, and how dysfunctional ciliary signaling contributes to pathogenesis. By focusing on signaling pathways that are mediated by the primary cilium, we can (a) leverage advances in human genetics associated with ciliopathies to drive new hypotheses, (b) exploit the specific localization of ciliary receptors to mechanistically interrogate these signaling pathways, and (c) begin to understand how the primary cilium integrates signals for binary cell fate decisions.

Selected Publications:

  1. Hilgendorf, K.I., Johnson, C.T., Mezger, A., Rice, S.L., Norris, A.M., Demeter, J., Greenleaf, W.J., Reiter, J.F., Kopinke, D., and Jackson, P.K. (2019). Omega-3 fatty acids activate ciliary FFAR4 to control adipogenesis. Cell. 179(6), 1289-1305. PMID: 31761534

  2. Hilgendorf, K.I., Johnson, C.T. & Jackson, P.K. (2016). The primary cilium as a cellular receiver: organizing ciliary GPCR signaling. Current Opinion in Cell Biology, 39, 84-92. PMID: 26926036

  3. Maynard, M.A., Ferretti, R., Hilgendorf, K.I., Perret, C. Whyte, P., and Lees, J.A. (2014). Bmi1 is required for tumorigenesis in a mouse model of intestinal cancer. Oncogene. 33(28), 3742-3747. PMID: 23955081

  4. Hilgendorf, K.I., Leshchiner, E.S., Nedelcu, S., Maynard, M.A., Calo, E., Ianari, A., Walensky, L.D., and Lees, J.A. (2013). The retinoblastoma protein induces apoptosis directly at the mitochondria. Genes & Development, 27(9), 1003-1015. PMID: 23618872.

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Last Updated: 7/10/20