4.6 Article

New tools for studying osteoarthritis genetics in zebrafish

Journal

OSTEOARTHRITIS AND CARTILAGE
Volume 21, Issue 2, Pages 269-278

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.joca.2012.11.004

Keywords

Zebrafish; Gene expression; Cartilage; Bone; Model; Osteoarthritis

Funding

  1. Arthritis Research UK
  2. FP7 TREAT OA
  3. Smart Mix Programme of the Netherlands Ministry of Economic Affairs and the Netherlands Ministry of Education, Culture and Science
  4. Versus Arthritis [19476] Funding Source: researchfish

Ask authors/readers for more resources

Objective: Increasing evidence points to a strong genetic component to osteoarthritis (OA) and that certain changes that occur in osteoarthritic cartilage recapitulate the developmental process of endochondral ossification. As zebrafish are a well validated model for genetic studies and developmental biology, our objective was to establish the spatiotemporal expression pattern of a number of OA susceptibility genes in the larval zebrafish providing a platform for functional studies into the role of these genes in OA. Design: We identified the zebrafish homologues for Mcf2l, Gdf5, PthrP/Pthlh, Co19a2, and Col10a1 from the Ensembl genome browser. Labelled probes were generated for these genes and in situ hybridisations were performed on wild type zebrafish larvae. In addition, we generated transgenic reporter lines by modification of bacterial artificial chromosomes (BACs) containing full length promoters for col2a1 and col10a1. Results: For the first time, we show the spatiotemporal expression pattern of Mcf2l. Furthermore, we show that all six putative OA genes are dynamically expressed during zebrafish larval development, and that all are expressed in the developing skeletal system. Furthermore, we demonstrate that the transgenic reporters we have generated for col2a1 and col10al can be used to visualise chondrocyte hypertrophy in vivo. Conclusion: In this study we describe the expression pattern of six OA susceptibility genes in zebrafish larvae and the generation of two new transgenic lines marking chondrocytes at different stages of maturation. Moreover, the tools used demonstrate the utility of the zebrafish model for functional studies on genes identified as playing a role in OA. (C) 2012 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Review Endocrinology & Metabolism

Skeletal Biology and Disease Modeling in Zebrafish

Kristin Dietrich, Imke A. K. Fiedler, Anastasia Kurzyukova, Alejandra C. Lopez-Delgado, Lucy M. McGowan, Karina Geurtzen, Chrissy L. Hammond, Bjorn Busse, Franziska Knopf

Summary: Zebrafish, as teleosts, share common features with mammals in terms of skeletal elements and ossification mechanisms, but differences exist in bone morphology and function. They have high regenerative capacity and complex bone formation mechanisms, making them suitable for skeletal research.

JOURNAL OF BONE AND MINERAL RESEARCH (2021)

Article Cell Biology

Transformed notochordal cells trigger chronic wounds in zebrafish, destabilizing the vertebral column and bone homeostasis

Paco Lopez-Cuevas, Luke Deane, Yushi Yang, Chrissy L. Hammond, Erika Kague

Summary: Notochordal cells play a critical role in vertebral column patterning, and their transformation can disrupt bone development and intervertebral disc stability. Transformed notochord cells in zebrafish skeleton cause damage and activate a chronic wound response, indicating parallels between chordomas, wounds, IVD degeneration, and inflammation.

DISEASE MODELS & MECHANISMS (2021)

Article Cell & Tissue Engineering

Exposure to hypergravity during zebrafish development alters cartilage material properties and strain distribution

E. A. Lawrence, J. Aggleton, J. van Loon, J. Godivier, R. Harniman, J. Pei, N. Nowlan, C. Hammond

Summary: The study found that exposure to hypergravity affects the material properties of cartilage and chondrocyte morphology in zebrafish, leading to changes in cartilage structure and function.

BONE & JOINT RESEARCH (2021)

Article Endocrinology & Metabolism

Opportunities and Challenges in Functional Genomics Research in Osteoporosis: Report From a Workshop Held by the Causes Working Group of the Osteoporosis and Bone Research Academy of the Royal Osteoporosis Society on October 5th 2020

Jonathan H. Tobias, Emma L. Duncan, Erika Kague, Chrissy L. Hammond, Celia L. Gregson, Duncan Bassett, Graham R. Williams, Josine L. Min, Tom R. Gaunt, David Karasik, Claes Ohlsson, Fernando Rivadeneira, James R. Edwards, Fadil M. Hannan, John P. Kemp, Sophie J. Gilbert, Nerea Alonso, Neelam Hassan, Juliet E. Compston, Stuart H. Ralston

Summary: Recent advancements in identifying the role of sclerostin in sclerosteosis have led to the development of anti-sclerostin antibodies as a novel treatment for osteoporosis. Despite the discovery of numerous genetic signals associated with bone mass, the challenge remains in accurately pinpointing the responsible genes and identifying potential drug targets for further treatment.

FRONTIERS IN ENDOCRINOLOGY (2021)

Article Biochemistry & Molecular Biology

Pharmacological Manipulation of Early Zebrafish Skeletal Development Shows an Important Role for Smad9 in Control of Skeletal Progenitor Populations

Georgina L. K. McDonald, Mengdi Wang, Chrissy L. Hammond, Dylan J. M. Bergen

Summary: Osteoporosis and other conditions related to low bone density are becoming more prevalent as the population ages and glucocorticoid use increases. Research suggests that targeting genes associated with high bone mass, such as SMAD9, could offer potential for future osteoanabolic therapies.

BIOMOLECULES (2021)

Article Cell Biology

Giantin is required for intracellular N-terminal processing of type I procollagen

Nicola L. Stevenson, Dylan J. M. Bergen, Yinhui Lu, M. Esther Prada-Sanchez, Karl E. Kadler, Chrissy L. Hammond, David J. Stephens

Summary: Knockout of the golgin giantin leads to skeletal and craniofacial defects due to changes in glycosylation and extracellular matrix deposition. Our study reveals a conserved role for giantin in collagen biosynthesis and extracellular matrix assembly, as well as a giantin-dependent pathway for intracellular procollagen processing.

JOURNAL OF CELL BIOLOGY (2021)

Article Multidisciplinary Sciences

Vangl2 promotes the formation of long cytonemes to enable distant Wnt/β-catenin signaling

Lucy Brunt, Gediminas Greicius, Sally Rogers, Benjamin D. Evans, David M. Virshup, Kyle C. A. Wedgwood, Steffen Scholpp

Summary: Vangl2 regulates Wnt ligand distribution by controlling cytoneme behavior, enhancing paracrine Wnt/β-catenin signaling. This study reveals the crucial role of Vangl2 in intercellular Wnt signal transduction through cytonemes.

NATURE COMMUNICATIONS (2021)

Review Hematology

Towards manufactured red blood cells for the treatment of inherited anemia

Stephanie Pellegrin, Charlotte E. Severn, Ashley M. Toye

Summary: This review discusses recent progress in the erythroid culture field as well as opportunities for further scaling up of manufactured RBC production for transfusion practice.

HAEMATOLOGICA (2021)

Article Biology

Regenerating zebrafish scales express a subset of evolutionary conserved genes involved in human skeletal disease

Dylan J. M. Bergen, Qiao Tong, Ankit Shukla, Elis Newham, Jan Zethof, Mischa Lundberg, Rebecca Ryan, Scott E. Youlten, Monika Frysz, Peter I. Croucher, Gert Flik, Rebecca J. Richardson, John P. Kemp, Chrissy L. Hammond, Juriaan R. Metz

Summary: Dermal scales possess a strong osteogenic expression profile similar to bone, enriched in genes favoring collagen matrix growth. Despite differences in developmental processes between scale and endoskeleton, zebrafish scales express a subset of evolutionarily conserved genes relevant to human skeletal diseases.

BMC BIOLOGY (2022)

Article Biochemical Research Methods

Dominating lengthscales of zebrafish collective behaviour

Yushi Yang, Francesco Turci, Erika Kague, Chrissy L. Hammond, John Russo, C. Patrick Royall

Summary: In this study, the collective behavior of 50 zebrafish was investigated in a three-dimensional manner. The researchers found that the fish exhibited a transition from ordered to random behavior when they adapted to new environmental conditions. By quantifying the spatial and temporal correlation functions, the researchers identified two length scales that captured the essence of these behavioral changes. The ratio of these length scales was found to correlate with the polarization of collective motion, which was explained using a simplified model of self-propelled particles with alignment interactions.

PLOS COMPUTATIONAL BIOLOGY (2022)

Article Anatomy & Morphology

Growth orientations, rather than heterogeneous growth rates, dominate jaw joint morphogenesis in the larval zebrafish

Josepha Godivier, Elizabeth A. Lawrence, Mengdi Wang, Chrissy L. Hammond, Niamh C. Nowlan

Summary: This study quantified key cellular dynamics involved in growth and morphogenesis of the zebrafish jaw joint and used computational simulations to predict joint development, highlighting the dominant influence of growth anisotropy on joint growth and morphogenesis. The findings contribute to understanding the pathogenesis of developmental joint disorders.

JOURNAL OF ANATOMY (2022)

Article Chemistry, Multidisciplinary

Macrophage Reprogramming with Anti-miR223-Loaded Artificial Protocells Enhances In Vivo Cancer Therapeutic Potential

Paco Lopez-Cuevas, Can Xu, Charlotte E. Severn, Tiah C. L. Oates, Stephen J. Cross, Ashley M. Toye, Stephen Mann, Paul Martin

Summary: This study demonstrates that silencing or knocking out a specific immune cell-expressed miRNA, microRNA-223 (miR223), can reduce cancer progression. By using miniature artificial protocells (PCs) to deliver anti-inflammatory miRNAs, the interactions between immune cells and cancer cells are altered, resulting in reduced tumor burden.

ADVANCED SCIENCE (2022)

Article Cell & Tissue Engineering

Osteomodulin downregulation is associated with osteoarthritis development

Jeremie Zappia, Qiao Tong, Renee Van der Cruyssen, Frederique M. F. Cornelis, Cecile Lambert, Tiago Pinto Coelho, Juliane Grisart, Erika Kague, Rik J. Lories, Marc Muller, Dirk Elewaut, Chrissy L. Hammond, Christelle Sanchez, Yves Henrotin

Summary: Abnormal subchondral bone remodeling leading to sclerosis is a main feature of osteoarthritis. Osteomodulin (OMD), a proteoglycan, is associated with the sclerotic phenotype. This study found that OMD binds to RANKL and inhibits osteoclastogenesis, thus regulating bone remodeling and contributing to bone and cartilage homeostasis. Targeting OMD may be a promising personalized approach for osteoarthritis.

BONE RESEARCH (2023)

Article Cell & Tissue Engineering

3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease

Erika Kague, Francesco Turci, Elis Newman, Yushi Yang, Kate Robson Brown, Mona S. Aglan, Ghada A. Otaify, Samia A. Temtamy, Victor L. Ruiz-Perez, Stephen Cross, C. Patrick Royall, P. Eckhard Witten, Chrissy L. Hammond

Summary: Back pain is a common condition with high social impact, largely attributed to intervertebral disc disease (IVDD). The role of bone mineral density (BMD) in IVDD remains controversial, with genetic components potentially influencing the disease. Using an aging zebrafish model, it was found that increased BMD in aging can lead to changes resembling osteoporosis, and mutations in sp7 and cathepsin K affecting BMD levels also impacted the development of IVDD.

BONE RESEARCH (2021)

Article Endocrinology & Metabolism

Wnt16 Elicits a Protective Effect Against Fractures and Supports Bone Repair in Zebrafish

Lucy M. McGowan, Erika Kague, Alistair Vorster, Elis Newham, Stephen Cross, Chrissy L. Hammond

Summary: In this study, CRISPR-Cas9 was used to generate mutant zebrafish lacking Wnt16 to investigate its effect on bone. The results suggest that Wnt16 plays a crucial role in bone health and repair by modulating canonical Wnt activity to facilitate osteoblast differentiation and bone matrix deposition.

JBMR PLUS (2021)

No Data Available