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Cilia

Cell Biology is home to one of the largest concentrations of cilia researchers in the United States. The primary ciliuma solitary, antenna-like organelle present on nearly every human cell plays a specialized and critical role in cellular signaling. Acting as a central hub for both chemo- and mechanosensory pathways, primary cilia regulate key signaling systems, including Hedgehog, Wnt, and G protein–coupled receptor (GPCR) pathways. Over the past two decades, dysfunction of this tiny yet essential cellular structure has been linked to more than 35 human diseases and syndromes, such as obesity and diabetes, polycystic kidney disease, brain malformations, cardiovascular disorders, skeletal abnormalities, and cancer. Our seven NIH-funded, cilia-focused laboratories use a wide range of experimental approaches and model systems to investigate the structure, formation, and function of primary cilia, advancing our understanding of their roles in health and disease.

Our Cilia Working Group meets monthly for data sharing, troubleshooting, and current literature discussions, fostering collaboration across labs and model systems. Trainees benefit from mentorship across complementary systems and techniques, and exposure to the full spectrum of cilia biology, from basic structure to human disease.

Our investigators

Dr. Huxing Cui

Dr. Huxing Cui applies mouse genetics and modern neuroscience approaches to investigate hypothalamic circuits and signaling mechanisms that regulate body homeostasis.

Dr. Tomoharu Kanie

Dr. Tomoharu Kanie deciphers the molecular mechanisms of the early step of cilium formation using cutting-edge imaging tools, including super-resolution microscopy.

Dr. Rosalia Paterno

Dr. Rosalia Paterno investigates the role of inhibitory interneurons in neuronal circuit development underlying autism spectrum disorder and related neurodevelopmental disorders, using interdisciplinary approaches in molecular, cellular, and systems neuroscience.

Dr. Leonidas Tsiokas

Dr. Leonidas Tsiokas investigates the functions of genes involved in polycystic kidney disease, a classic ciliopathy, using a variety of techniques, including mouse genetics, calcium imaging, and bioluminescence-based assays.

Dr. Julie Van De Weghe

Dr. Julie Van De Weghe studies the mechanisms underlying ciliopathy conditions and the functions of the Joubert syndrome-related genes in both Chlamydomonas reinhardtii and human cells.

Dr. Xinxing Zhang

Dr. Xinxing Zhang studies the role of ciliary GPCRs in neuronal homeostasis using C. elegans and mice.

Dr. Kurt Zimmerman

Dr. Kurt Zimmerman investigates the role of immune cells in cystic kidney diseases using advanced mouse genetic models, flow cytometry, and single cell RNA sequencing.

Contact Us

Department of Cell Biology

Sean Netterville | Admin Coordinator
940 Stanton L. Young Blvd, BMSB 553
Oklahoma City, OK 73104-53036

(405) 271-2377
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Fax:(405) 271-3548