Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia
Background: Beyond its structural role in the skeleton, the extracellular matrix (ECM), particularly basement membrane proteins, facilitates communication with intracellular signaling pathways and cell to cell interactions to control differentiation, proliferation, migration and survival. Alteration...
| Main Authors: | , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
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Elsevier
2020-12-01
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| Series: | EBioMedicine |
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| Online Access: | http://www.sciencedirect.com/science/article/pii/S2352396420304515 |
| _version_ | 1818721408636682240 |
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| author | Maya Barad Fabiana Csukasi Michaela Bosakova Jorge H. Martin Wenjuan Zhang S. Paige Taylor Ralph S. Lachman Jennifer Zieba Michael Bamshad Deborah Nickerson Jessica X. Chong Daniel H. Cohn Pavel Krejci Deborah Krakow Ivan Duran |
| author_facet | Maya Barad Fabiana Csukasi Michaela Bosakova Jorge H. Martin Wenjuan Zhang S. Paige Taylor Ralph S. Lachman Jennifer Zieba Michael Bamshad Deborah Nickerson Jessica X. Chong Daniel H. Cohn Pavel Krejci Deborah Krakow Ivan Duran |
| author_sort | Maya Barad |
| collection | DOAJ |
| description | Background: Beyond its structural role in the skeleton, the extracellular matrix (ECM), particularly basement membrane proteins, facilitates communication with intracellular signaling pathways and cell to cell interactions to control differentiation, proliferation, migration and survival. Alterations in extracellular proteins cause a number of skeletal disorders, yet the consequences of an abnormal ECM on cellular communication remains less well understood Methods: Clinical and radiographic examinations defined the phenotype in this unappreciated bent bone skeletal disorder. Exome analysis identified the genetic alteration, confirmed by Sanger sequencing. Quantitative PCR, western blot analyses, immunohistochemistry, luciferase assay for WNT signaling were employed to determine RNA, proteins levels and localization, and dissect out the underlying cell signaling abnormalities. Migration and wound healing assays examined cell migration properties. Findings: This bent bone dysplasia resulted from biallelic mutations in LAMA5, the gene encoding the alpha-5 laminin basement membrane protein. This finding uncovered a mechanism of disease driven by ECM-cell interactions between alpha-5-containing laminins, and integrin-mediated focal adhesion signaling, particularly in cartilage. Loss of LAMA5 altered β1 integrin signaling through the non-canonical kinase PYK2 and the skeletal enriched SRC kinase, FYN. Loss of LAMA5 negatively impacted the actin cytoskeleton, vinculin localization, and WNT signaling. Interpretation: This newly described mechanism revealed a LAMA5-β1 Integrin-PYK2-FYN focal adhesion complex that regulates skeletogenesis, impacted WNT signaling and, when dysregulated, produced a distinct skeletal disorder. Funding: Supported by NIH awards R01 AR066124, R01 DE019567, R01 HD070394, and U54HG006493, and Czech Republic grants INTER-ACTION LTAUSA19030, V18-08-00567 and GA19-20123S. |
| first_indexed | 2024-12-17T20:38:16Z |
| format | Article |
| id | doaj.art-92542388a0ba41a0b688700973236fab |
| institution | Directory Open Access Journal |
| issn | 2352-3964 |
| language | English |
| last_indexed | 2024-12-17T20:38:16Z |
| publishDate | 2020-12-01 |
| publisher | Elsevier |
| record_format | Article |
| series | EBioMedicine |
| spelling | doaj.art-92542388a0ba41a0b688700973236fab2022-12-21T21:33:24ZengElsevierEBioMedicine2352-39642020-12-0162103075Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasiaMaya Barad0Fabiana Csukasi1Michaela Bosakova2Jorge H. Martin3Wenjuan Zhang4S. Paige Taylor5Ralph S. Lachman6Jennifer Zieba7Michael Bamshad8Deborah Nickerson9Jessica X. Chong10Daniel H. Cohn11Pavel Krejci12Deborah Krakow13Ivan Duran14Department of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United StatesDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United States; Laboratory of Bioengineering and Tissue Regeneration-LABRET, Department of Cell Biology, Genetics and Physiology, University of Málaga, IBIMA, Málaga 29071, SpainDepartment of Biology, Faculty of Medicine, Masaryk University, Brno 62500, Czech Republic; International Clinical Research Center, St. Anne's University Hospital, Brno 65691, Czech RepublicDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United StatesDepartment of Molecular, Cell and Developmental Biology, University of California– Los Angeles, Los Angeles, CA 90095, United StatesDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United StatesInternational Skeletal Dysplasia Registry, University of California, Los Angeles, CA 90095 United StatesDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United StatesUniversity of Washington Center for Mendelian Genomics, University of Washington, Seattle, WA 98195 United StatesUniversity of Washington Center for Mendelian Genomics, University of Washington, Seattle, WA 98195 United StatesUniversity of Washington Center for Mendelian Genomics, University of Washington, Seattle, WA 98195 United StatesDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United States; Department of Molecular, Cell and Developmental Biology, University of California– Los Angeles, Los Angeles, CA 90095, United States; Orthopaedic Institute for Children, University of California–Los Angeles, Los Angeles, CA 90095, United StatesDepartment of Biology, Faculty of Medicine, Masaryk University, Brno 62500, Czech Republic; International Clinical Research Center, St. Anne's University Hospital, Brno 65691, Czech RepublicDepartment of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United States; International Skeletal Dysplasia Registry, University of California, Los Angeles, CA 90095 United States; Orthopaedic Institute for Children, University of California–Los Angeles, Los Angeles, CA 90095, United States; Department of Human Genetics, University of California–Los Angeles, Los Angeles, CA 90095, United States; Department of Obstetrics and Gynecology, University of California–Los Angeles, Los Angeles, CA 90095, United States; Corresponding author.Department of Orthopaedic Surgery, University of California–Los Angeles, 615 Charles E. Young Drive South, BSRB 512, Los Angeles, CA 90095, United States; Laboratory of Bioengineering and Tissue Regeneration-LABRET, Department of Cell Biology, Genetics and Physiology, University of Málaga, IBIMA, Málaga 29071, Spain; Networking Biomedical Research Center in Bioengineering, Biomaterials and Nanomedicine (CIBER-BBN), Andalusian Centre for Nanomedicine and Biotechnology-BIONAND, Severo Ochoa 35, Málaga 29590, SpainBackground: Beyond its structural role in the skeleton, the extracellular matrix (ECM), particularly basement membrane proteins, facilitates communication with intracellular signaling pathways and cell to cell interactions to control differentiation, proliferation, migration and survival. Alterations in extracellular proteins cause a number of skeletal disorders, yet the consequences of an abnormal ECM on cellular communication remains less well understood Methods: Clinical and radiographic examinations defined the phenotype in this unappreciated bent bone skeletal disorder. Exome analysis identified the genetic alteration, confirmed by Sanger sequencing. Quantitative PCR, western blot analyses, immunohistochemistry, luciferase assay for WNT signaling were employed to determine RNA, proteins levels and localization, and dissect out the underlying cell signaling abnormalities. Migration and wound healing assays examined cell migration properties. Findings: This bent bone dysplasia resulted from biallelic mutations in LAMA5, the gene encoding the alpha-5 laminin basement membrane protein. This finding uncovered a mechanism of disease driven by ECM-cell interactions between alpha-5-containing laminins, and integrin-mediated focal adhesion signaling, particularly in cartilage. Loss of LAMA5 altered β1 integrin signaling through the non-canonical kinase PYK2 and the skeletal enriched SRC kinase, FYN. Loss of LAMA5 negatively impacted the actin cytoskeleton, vinculin localization, and WNT signaling. Interpretation: This newly described mechanism revealed a LAMA5-β1 Integrin-PYK2-FYN focal adhesion complex that regulates skeletogenesis, impacted WNT signaling and, when dysregulated, produced a distinct skeletal disorder. Funding: Supported by NIH awards R01 AR066124, R01 DE019567, R01 HD070394, and U54HG006493, and Czech Republic grants INTER-ACTION LTAUSA19030, V18-08-00567 and GA19-20123S.http://www.sciencedirect.com/science/article/pii/S2352396420304515Laminin α5LAMA5Skeletal dysplasiaBent boneβ1 integrin |
| spellingShingle | Maya Barad Fabiana Csukasi Michaela Bosakova Jorge H. Martin Wenjuan Zhang S. Paige Taylor Ralph S. Lachman Jennifer Zieba Michael Bamshad Deborah Nickerson Jessica X. Chong Daniel H. Cohn Pavel Krejci Deborah Krakow Ivan Duran Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia EBioMedicine Laminin α5 LAMA5 Skeletal dysplasia Bent bone β1 integrin |
| title | Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| title_full | Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| title_fullStr | Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| title_full_unstemmed | Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| title_short | Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| title_sort | biallelic mutations in lama5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia |
| topic | Laminin α5 LAMA5 Skeletal dysplasia Bent bone β1 integrin |
| url | http://www.sciencedirect.com/science/article/pii/S2352396420304515 |
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