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Profile

Katrin Henke

  • Department of Orthopaedics
    Assistant Professor
  • katrin.henke@emory.edu
  • @KatrinHenkeLab
  • Lab Homepage
  • Google Scholar
Head shot of Katrin Henke

Overview

Our lab explores gene function during development, homeostasis and disease of the musculoskeletal system utilizing the zebrafish as a model. Zebrafish are widely used in biomedical research due to ease of genetic manipulation, high fecundity, external fertilization, rapid early development and transparency of early life stages. They show strong similarities with human physiology and in genetic architecture. While at first glance the skeleton of the zebrafish looks very different compared to a human skeleton, it contains the same major cell types and shows strong correlation in its structure and genetic regulation. Taking advantage of the many imaging, genetic and genomic tools in zebrafish and the diverse expertise in the Orthopaedics Department, we seek to gain crucial insight into musculoskeletal biology, disease etiology and progression to aid in the development of new treatments and therapeutic strategies.

Academic Appointment

  • Assistant Professor, Department of Human Genetics, Emory University School of Medicine
  • Assistant Professor, Department of Orthopaedics, Emory University School of Medicine

Education

Degrees

  • PhD from Max Planck Institute for Developmental Biology
  • M.Sc. in Molecular Medicine from University of Erlangen-Nuremberg

Research

Publications

  • Inhibition of KDM2/7 Promotes Notochordal Differentiation of hiPSCs.
    Cells Volume: 13
    09/04/2024 Authors: Diaz-Hernandez ME; Murakami K; Murata S; Khan NM; Shenoy SPV; Henke K; Yamada H; Drissi H
  • Current perspectives on the multiple roles of osteoclasts: Mechanisms of osteoclast-osteoblast communication and potential clinical implications.
    Elife Volume: 13
    04/09/2024 Authors: Daponte V; Henke K; Drissi H
  • The RNA-binding protein Adad1 is necessary for germ cell maintenance and meiosis in zebrafish.
    PLoS Genet Volume: 19 Page(s): e1010589
    08/01/2023 Authors: Islam KN; Ajao A; Venkataramani K; Rivera J; Pathania S; Henke K; Siegfried KR
  • Loss of lrp5 in zebrafish reveals unexpected role of Lrp5 in osteoclast regulation
    Volume: 38 Page(s): 279 - 280
    02/01/2023 Authors: Khrystoforova I; Shochat-Carvalho C; Harari R; David K; Henke K; Woronowicz K; Harris M
  • Genetically engineered zebrafish as models of skeletal development and regeneration.
    Bone Volume: 167 Page(s): 116611
    02/01/2023 Authors: Henke K; Farmer DT; Niu X; Kraus JM; Galloway JL; Youngstrom DW
  • Resolving primary pathomechanisms driving idiopathic-like spinal curvature using a new katnb1 scoliosis model.
    iScience Volume: 25 Page(s): 105028
    09/16/2022 Authors: Meyer-Miner A; Van Gennip JLM; Henke K; Harris MP; Ciruna B
  • Zebrafish mutants reveal unexpected role of Lrp5 in osteoclast regulation.
    Front Endocrinol (Lausanne) Volume: 13 Page(s): 985304
    01/01/2022 Authors: Khrystoforova I; Shochat-Carvalho C; Harari R; Henke K; Woronowicz K; Harris MP; Karasik D
  • Latent developmental potential to form limb-like skeletal structures in zebrafish.
    Cell Volume: 184 Page(s): 899 - 911.e13
    02/18/2021 Authors: Hawkins MB; Henke K; Harris MP
  • Notochordal Signals Establish Phylogenetic Identity of the Teleost Spine.
    Curr Biol Volume: 30 Page(s): 2805 - 2814.e3
    07/20/2020 Authors: Peskin B; Henke K; Cumplido N; Treaster S; Harris MP; Bagnat M; Arratia G
  • SCO-Spondin Defects and Neuroinflammation Are Conserved Mechanisms Driving Spinal Deformity across Genetic Models of Idiopathic Scoliosis.
    Curr Biol Volume: 30 Page(s): 2363 - 2373.e6
    06/22/2020 Authors: Rose CD; Pompili D; Henke K; Van Gennip JLM; Meyer-Miner A; Rana R; Gobron S; Harris MP; Nitz M; Ciruna B
  • celsr1a is essential for tissue homeostasis and onset of aging phenotypes in the zebrafish.
    Elife Volume: 9
    01/27/2020 Authors: Li C; Barton C; Henke K; Daane J; Treaster S; Caetano-Lopes J; Tanguay RL; Harris MP
  • Unique and non-redundant function of csf1r paralogues in regulation and evolution of post-embryonic development of the zebrafish.
    Development Volume: 147
    01/22/2020 Authors: Caetano-Lopes J; Henke K; Urso K; Duryea J; Charles JF; Warman ML; Harris MP
  • A role for G protein-coupled receptor 137b in bone remodeling in mouse and zebrafish.
    Bone Volume: 127 Page(s): 104 - 113
    10/01/2019 Authors: Urso K; Caetano-Lopes J; Lee PY; Yan J; Henke K; Sury M; Liu H; Zgoda M; Jacome-Galarza C; Nigrovic PA
  • Clearance by Microglia Depends on Packaging of Phagosomes into a Unique Cellular Compartment.
    Dev Cell Volume: 49 Page(s): 77 - 88.e7
    04/08/2019 Authors: Villani A; Benjaminsen J; Moritz C; Henke K; Hartmann J; Norlin N; Richter K; Schieber NL; Franke T; Schwab Y
  • Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies.
    Proc Natl Acad Sci U S A Volume: 115 Page(s): E8037 - E8046
    08/21/2018 Authors: Gistelinck C; Kwon RY; Malfait F; Symoens S; Harris MP; Henke K; Hawkins MB; Fisher S; Sips P; Guillemyn B
  • Cyclin-dependent kinase 21 is a novel regulator of proliferation and meiosis in the male germline of zebrafish.
    Reproduction Volume: 157 Page(s): 383 - 398
    04/01/2018 Authors: Webster KA; Henke K; Ingalls DM; Nahrin A; Harris MP; Siegfried KR
  • Phenomic analysis of zebrafish type I collagen mutants reveals a spectrum of skeletal phenotypes mimicking the clinical variability in human brittle bone disease
    Volume: 32 Page(s): S319 - S319
    12/01/2017 Authors: Gistelinck C; Kwon RY; Malfait F; Symoens S; Vermassen P; De Saffel H; Henke K; Harris MP; De Paepe A; Weis M
  • Genetic Screen for Postembryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form.
    Genetics Volume: 207 Page(s): 609 - 623
    10/01/2017 Authors: Henke K; Daane JM; Hawkins MB; Dooley CM; Busch-Nentwich EM; Stemple DL; Harris MP
  • Utility of quantitative micro-computed tomographic analysis in zebrafish to define gene function during skeletogenesis.
    Bone Volume: 101 Page(s): 162 - 171
    08/01/2017 Authors: Charles JF; Sury M; Tsang K; Urso K; Henke K; Huang Y; Russell R; Duryea J; Harris MP
  • Extracellular matrix of cranial sutures reveals common mechanisms of their formation between fish and man
    Volume: 167 Page(s): 1465 - 1466
    07/01/2015 Authors: Henke K; Yorlets R; Meara J; Proctor M; Harris MP
  • The SLC7A7 Transporter Identifies Microglial Precursors prior to Entry into the Brain.
    Cell Rep Volume: 11 Page(s): 1008 - 1017
    05/19/2015 Authors: Rossi F; Casano AM; Henke K; Richter K; Peri F
  • A Genetic Model to Understand Integration During Skull Development and Etiology of Craniofacial Disorders
    Volume: 29
    04/01/2015 Authors: Harris M; Henke K
  • Katanin p80 regulates human cortical development by limiting centriole and cilia number.
    Neuron Volume: 84 Page(s): 1240 - 1257
    12/17/2014 Authors: Hu WF; Pomp O; Ben-Omran T; Kodani A; Henke K; Mochida GH; Yu TW; Woodworth MB; Bonnard C; Raj GS
  • Quantitative Micro-CT Analysis of Bone in Zebrafish: Accessing an Untapped Resource.
    Volume: 29 Page(s): S350 - S350
    02/01/2014 Authors: Charles J; Henke K; Tsang K; Russell R; Harris MP; Duryea J; Aliprantis A
  • Identification of mutations in zebrafish using next-generation sequencing.
    Curr Protoc Mol Biol Volume: 104 Page(s): 7.13.1 - 7.13.33
    10/11/2013 Authors: Henke K; Bowen ME; Harris MP
  • Perspectives for identification of mutations in the zebrafish: making use of next-generation sequencing technologies for forward genetic approaches.
    Methods Volume: 62 Page(s): 185 - 196
    08/15/2013 Authors: Henke K; Bowen ME; Harris MP
  • Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein.
    J Clin Endocrinol Metab Volume: 97 Page(s): E2140 - E2151
    11/01/2012 Authors: Dauber A; Lafranchi SH; Maliga Z; Lui JC; Moon JE; McDeed C; Henke K; Zonana J; Kingman GA; Pers TH
  • Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing.
    Genetics Volume: 190 Page(s): 1017 - 1024
    03/01/2012 Authors: Bowen ME; Henke K; Siegfried KR; Warman ML; Harris MP
  • Microglia in the developing brain: from immunity to behaviour.
    Curr Opin Neurobiol Volume: 21 Page(s): 5 - 10
    02/01/2011 Authors: Schlegelmilch T; Henke K; Peri F
  • Isolation and characterization of molecules involved in macrophage migration to and colonization of the zebrafish brain
    Volume: 306 Page(s): 432 - 432
    06/01/2007 Authors: Henke K; Peri F; Nuesslein-Volhard C
  • Identification of G protein-coupled receptor 137B (GPR137b) function in mouse and zebrafish osteoclasts
    Page(s): 199 - 199
    Authors: Urso K; Caetano-Lopes J; Lee P; Henke K; Aliprantis AO; Charles JF; Warman ML; Harris MP
  • Identification of G protein-coupled receptor 137B (GPR137b) function in mouse and zebrafish osteoclasts
    Page(s): 199 - 199
    Authors: Urso K; Caetano-Lopes J; Lee P; Henke K; Aliprantis AO; Charles JF; Warman ML; Harris MP
  • Colony-stimulating factor 1 receptor a (Csf1ra)-deficient zebrafish as a model of unbalanced bone remodeling
    Volume: 5 Page(s): P458 - P458
    Authors: Caetano-Lopes J; Urso K; Henke K; Aliprantis AO; Charles JF; Warman ML; Harris MP
  • Colony-stimulating factor 1 receptor a (Csf1ra)-deficient zebrafish as a model of unbalanced bone remodeling
    Volume: 5 Page(s): P458 - P458
    Authors: Caetano-Lopes J; Urso K; Henke K; Aliprantis AO; Charles JF; Warman ML; Harris MP
  • Chloride channel voltage-sensitive 7 (CLCN7) loss-of-function zebrafish as a genetic model of osteoclast-rich osteopetrosis

    Authors: Urso K; Caetano-Lopes J; Sury M; Henke K; Aliprantis AO; Warman ML; Duryea J; Harris MP; Charles JF
  • Chloride channel voltage-sensitive 7 (CLCN7) loss-of-function zebrafish as a genetic model of osteoclast-rich osteopetrosis

    Authors: Urso K; Caetano-Lopes J; Sury M; Henke K; Aliprantis AO; Warman ML; Duryea J; Harris MP; Charles JF
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