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Gabsang Lee, Ph.D.

Assistant Professor of Neurology

Male

Titles

  • Assistant Professor of Neurology
  • Assistant Professor of Neuroscience

Centers & Institutes

Departments

Contact for Research Inquiries

Phone: 443-287-8631

Expertise

Muscular Dystrophies, Pain, Peripheral Nerve Disorders

Research Interests

Neural crest cell biology; Peripheral nerves disease; Congenital Insensitivity of Pain and Anhidrosis; Familial Dysautonomia; Charcot-Marie-Tooth 1A; Skeletal muscle; Duchenne muscular dystrophy; Facioscapulohumeral muscular dystrophy

Biography

Dr. Lee is currently Assistant Professor in the Department of Neurology and Neuroscience at Johns Hopkins School of Medicine, where he continues his research on peripheral nerve disease (Charcot-Marie-Tooth, Congenital insensitivity to Pain and Anhidrosis, Familial Dysautonomia) and muscular dystrophies (Duchenne muscular dystrophies, Facioscapulohumeral muscular dystrophies). His lab has established a novel methodology for direct derivation and prospective isolation of peripheral neurons, Schwann cells and skeletal muscle, from human pluripotent stem cells of diseases. Using these patient-specific model, they are studying disease mechanism and testing therapeutic compounds. 

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Featured Video

Gabsang Lee | Using Patient's Stem Cells to Study Peripheral Nervous System Diseases

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    Additional Information

  • Education +
    • B.S., Seoul National University (Korea) (2000)
    • Ph.D., Seoul National University (Korea) (2004)
  • Research & Publications +

    Research Summary

    Human induced pluripotent stem cells (hiPSCs) now provide unprecedented opportunities for cell replacement approaches, disease modeling and drug discovery in patient-specific manner. Particularly Lee lab is focusing on neural crest lineage (including peripheral neurons, Schwann cells, melanocytes) and skeletal muscle.

    Neural crest, autonomic neurons and Familial Dysautonomia
    Previously, our group studied neural crest stem cells created from fibroblasts of patients with Familial Dysautonomia (FD), also known as Riley-Day syndrome, an inherited genetic condition that affects the peripheral nervous system. Although researchers know that FD is caused by a single point mutation in the IKBKAP gene, it is not clear how symptoms, like inability to feel pain and changes in temperature, manifest. We found that FD-specific neural crest cells expressed low levels of genes needed to make autonomous neurons—the ones needed for the “fight-or-flight” response. The FD-specific neural crest cells also moved around less than normal neural crest cells. Moving forward, as an effort to discover novel drugs to treat FD, we performed high throughput screening with a compound library using FD patient-derived neural crest stem cells to look for compounds that increased gene expression and protein levels of autonomous neuron developmental components. These studies set a paradigm of hiPSC studies, including developing differentiation protocol, disease modeling with patient hiPSCs and high throughput drug screening. Now we are advancing from neural crest to autonomic neurons and multicellular system. Our PHOX2b::GFP+ sympathetic neurons and their functional connection to target tissues (cardiac syncytia), which will lead us to investigate aberrant neuromodulation in patient-specific manner.

    Nociceptive/pruriceptive neurons and congenital pain disorders
    How our body can sense million of different stimuli with limited numbers of sensory neurons? How our ‘sensors’ can perceive specific stimulus? The fate decision and physiological functions of individual sensory neurons should be choreographed by multiple molecular processes, which are closely related to the pathogenesis of many human pain disorders. Using iPSC lines of congenital sensory disorders, Congenital Insensitivity of Pain and Anhidrosis (CIPA) and Congenital Insensitivity of Pain (CIP), we are interrogating these questions with human TRPV1::GFP+ nociceptive and MRGPRX1::GFP+ pruriceptive neurons.


    Schwann cells and Charcot Marie Tooth 1A
    Charcot-Marie-Tooth 1A (CMT1A) is one of the most common genetic diseases in peripheral nervous system. We have learned lots of information from animal models, but their genetics are yet exactly same as those of CMT1A patients. Recently, in the Lee lab, the CMT1A-hiPSC-derived Schwann cells have provided us a new insight on the disease mechanism that is shared with Schwann cells derived from CMT1A-PDG-hESCs and induced neural crest of CMT1A fibroblasts.


    Skeletal muscle cells, in vitro myogenesis, and muscular dystrophies
    We developed a new methodology to directly derive and prospectively isolate thousands of millions of expandable and fusion-competent myoblasts from hESCs/hiPSCs. Using multiple genetic reporter hESC lines, we are recapitulating step-wise human myogenesis, comprising pluripotent stem cells, somite cells, adipomyocytes and putative satellite stem cells. Further, hiPSCs of Duchenne muscular dystrophy and facioscapulohumeral muscular dystrophy are providing us unique opportunities to learn more about the devastating muscular dystrophies.

    Lab Website: Gabsang Lee Lab

    CORE Facilities

    Stem Cell Core Facility

    Selected Publications

    Kim YJ, Lim HT, Li Z, Oh Y, Kovlyagina I, Choi IY, Dong XZ, Lee G*. Generation of multipotent induced neural crest by direct reprogramming of human postnatal fibroblasts with a single transcription factor. Cell Stem Cell. 2014;15:497-506. PMID 25158936 * Corresponding Author

    Lee G*, Ramirez CN, KimH, Zeltner N, Liu B, Radu C, Bhinder B, Kim YJ, Choi IY, Mukherjee-Clavin B, Djaballh H, Studer L*. Identification of Compounds that Rescue IKBKAP Expression in Familial Dysautonomia-iPS Cells. Nat Biotechnol. 201230:1244-1280. PMID 23159879 * Corresponding Author

    Lee G, Chambers SM, Tomishima MJ, Studer L. Derivation of Neural Crest Cells from Human Pluripotent Stem Cells. Nature Protocols 2010 5:688-701. (Cover image) PMID 20360764

    Lee G, Papapetrou EP, Kim HS, Chambers SM, Tomishima MJ, Fasano CA, Viale A, Tabar V, Sadlain M, Studer L. Modeling Pathogenesis and Treatment of Familial Dysautonomia using patient-specific iPSCs. Nature 2009 461: 402-406. PMID 19693009

    Lee GS, Kim HS, Elkabetz Y, Al Shamy G, Panagiotakos G, Barberi T, Tabar V, Studer L. Isolation and directed differentiation of neural crest stem cells derived from human embryonic stem cells. Nature Biotechnology 2007 25:1468-1475. PMID 18037878

  • Academic Affiliations & Courses +
  • Activities & Honors +

    Honors

    • Druckenmiller Fellowship (USA), New York Stem Cell Foundation, 2009 - 2011
    • Robertson Investigator, New York Stem Cell Foundation , 2011

    Memberships

    • International Society of Stem Cell Research (ISSCR), 2010
      Member
  • Videos & Media +

    Videos

    Stem Cells in Facioscapuloumeral Muscular Dystrophy research

    Recent News Articles & Media Coverage

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