Luis F Lopez-Santiago

headshot of Luis-Lopez-Santiago
Associate Research Scientist
Pharmacology
Medical School
University of Michigan Medical School
Pharmacology
2301C MSRB III, 1150 W. Medical Center drive
Ann Arbor, MI 48109
[email protected]
Available to mentor
Luis F Lopez-Santiago
headshot of Luis-Lopez-Santiago
Associate Research Scientist
  • About
  • Links
  • Qualifications
  • Research Overview
  • Recent Publications
  • Manage Your Profile

  • About

    Dr. Lopez-Santiago has been doing patch clamp electrophysiology for over 25 years, specializing in recording isolated ion currents and action potentials across various cell types to elucidate cellular excitability regulation mechanisms. His formal training in electrophysiology commenced during his Ph.D. studies, where he worked with cell lines and primary cultures under the guidance of Dr. Gabriel Cota. Subsequently, as a postdoctoral researcher in Dr. Lori Isom's laboratory at the University of Michigan, his expertise expanded through collaborations with numerous scientists. Over the years, Dr. Lopez-Santiago has worked extensively with various cell lines, acute dissociated neurons, cardiomyocytes, and iPSC-derived neurons, conducting a wide range of electrophysiological recordings. His expertise in electrophysiology has enabled successful collaborations with sodium channel biologicals and epilepsy experts such as Dr. Lori Isom, Dr. Jack Parent, Dr. Miriam Meisler and others at the University of Michigan.

    Dr. Lopez-Santiago and his collaborators have utilized cell lines to express genetic mutations in the SCN1B gene, investigating the mechanisms through which these mutations modify sodium currents. Additionally, they have used anomal models to explore mutations in SCN1B, SCN1A, and SCN8A, which are associated with Dravet syndrome and other severe epileptic encephalopathies. Furthermore, they have utilized human iPSC-derived neurons from epileptic patients to study how these genetic mutations alter sodium current and excitability in distinct genetic backgrounds and various neuron types. Their research also includes pharmacological studies aimed at developing more personalized treatments for individual patients.

    Links

    • Isom Lab Website

    Qualifications

    • Postdoctoral
      Michigan Medicine, Pharmacology, Ann Arbor, United States
      2003 - 2007
      Postdoctoral Research
    • PhD
      Department of Physiology, Biophysics and Neuroscience. Center for Research and Advanced Studies of IPN (CINVESTAV-IPN), Mexico, Mexico, Mexico
      1998 - 2002
    • MS
      Department of Physiology, Biophysics and Neuroscience. Center for Research and Advanced Studies of IPN (CINVESTAV-IPN), Mexico, Mexico, Mexico
      1995 - 1998
    • BSc
      School of Chemical Sciences; Benemeritus Autonomous University of Puebla, Puebla, Puebla, Mexico
      1990 - 1994

    Research Overview

    Genetic epilepsy; the influence of mutations in sodium channel genes on neuronal and cardiac physiology.

    Recent Publications

    See All Publications
    • Journal Article
      Altered cardiac excitability and arrhythmia in models of SCN1B-linked developmental and epileptic encephalopathy
      Ramos-Mondragon R, Wang S, Edokobi N, Liu Q, Qiao X, Shih M, Dang LT, Tsan YC, Štěrbová K, Helms AS, Weckhuysen S, Lopez-Santiago LF, Parent JM, Isom LL. Jci Insight, 2025 Sep 9; 10 (17): DOI:10.1172/jci.insight.190918
      PMID: 40763036
    • Journal Article
      Ataxia and cerebellar hypoexcitability in a mouse model of SCN1B-linked Dravet syndrome
      Yuan Y, O’Malley HA, Winters JJ, Lavado A, Denomme NS, Bakshi S, Hodges SL, Lopez-Santiago L, Chen C, Isom LL. Jci Insight, 2025 Sep 9; 10 (17): DOI:10.1172/jci.insight.187606
      PMID: 40923316
    • Presentation
      From Bench to Bedside: Translating Animal Model Research to Develop Novel Treatments for SUDEP Prevention
      Lopez-Santiago L. 2025 Feb 7;
    • Proceeding / Abstract / Poster
      Dravet Syndrome Patient Variant SCN1B p.R89C Alters Neuronal Membrane Electric Properties Leading to Hyperexcitability in Human iPSC-derived Excitatory Cortical Neurons.
      Yuan Y, Lopez-Santiago L, Dang L, Lin G, Swaminathan P, Vaid S, Loughman A, Tidball A, Štěrbová K, Weckhuysen S, DeJonghe P, Parent J, Isom L. 2024 Dec 6;
    • Journal Article
      Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model
      Yuan Y, Lopez-Santiago L, Denomme N, Chen C, O’Malley HA, Hodges SL, Ji S, Han Z, Christiansen A, Isom LL. Brain, 2024 Apr 1; 147 (4): 1231 - 1246. DOI:10.1093/brain/awad349
      PMID: 37812817
    • Proceeding / Abstract / Poster
      Sexual Dimorphic Differences in a Mouse Model of Scn1b-linked Epilepsy with Cardiac Arrhythmia
      Lopez-Santiago L, Ramos Mondragon R, Milton J, Isom L. 2023 Dec 1;
    • Proceeding / Abstract / Poster
      STK-001 surrogate restores the excitability of parvalbumin-positive fast-spiking interneurons in a mouse model of Dravet Syndrome.
      Lopez-Santiago L, Yuan Y, Denomme N, Chen C, Ji S, Han Z, Christiansen A, Liau G, Isom L. 2023 Jul 31;
    • Proceeding / Abstract / Poster
      Human Induced Pluripotent Stem Cell Model to Study Interneuron Defects in Dravet Syndrome
      Verma I, Yuan Y, Lopez-Santiago L, Uhler M, Isom L, Parent J. 2023 Jun 14;