Published May 31, 2020 | Version v1

Cartilage acidic protein 1 promotes increased cell viability, cell proliferation and energy metabolism in primary human dermal fibroblasts.

  • 1. Laboratory of Biochemistry, Scientific Affairs, APIVITA SA, Industrial Park of 5 Markopoulo Mesogaias, 19003, Markopoulo Attikis, Athens, Greece
  • 2. Comparative Endocrinology and Integrative Biology Group (CEIB),Centro de Ciencias do Mar (CCMAR), Universidade do Algarve, Campus de Gambelas, 8005-139, Faro, Portugal.
  • 3. Universidade do Algarve, Faculdade de Ciências e Tecnologia, 8005-139, Faro, Portugal - Instituto de Telecomunicações, Avenida Rovisco Pais 1, 1049-001, Lisboa, Portugal
  • 4. Comparative Endocrinology and Integrative Biology Group (CEIB),Centro de Ciencias do Mar (CCMAR), Universidade do Algarve, Campus de Gambelas, 8005-139, Faro, Portugal - Universidade do Algarve, Faculdade de Ciências e Tecnologia, 8005-139, Faro, Portugal

Description

Cartilage acidic protein 1 (CRTAC1) is an extracellular matrix protein of human chondrogenic tissue that is also present in other vertebrates, non-vertebrate eukaryotes and in some prokaryotes. The function of CRTAC1 remains unknown but the protein's structure indicates a role in cell-cell or cell-matrix interactions and calcium-binding. The aim of the present study was to evaluate the in vitro effects of hCRTAC1-A on normal human dermal fibroblasts (NHDF). A battery of in vitro assays (biochemical and PCR), immunofluorescence and a biosensor approach were used to characterize the protein's biological activities on NHDF cells in a scratch assay. Gene expression analysis revealed that hCRTAC1-A protein is associated with altered levels of expression for genes involved in the processes of cell proliferation (CXCL12 and NOS2), cell migration (AQP3 and TNC), and extracellular matrix-ECM regeneration and remodeling (FMOD, TIMP1, FN1) indicating a role for hCRTAC1-A in promoting these activities in a scratch assay. In parallel, the candidate processes identified by differential gene transcription were substantiated and extended using Electric cell-substrate impedance sensing (ECIS) technology, immunofluorescence and cell viability assays. Our findings indicate that hCRTAC1-A stimulated cell proliferation, migration and ECM production in primary human fibroblasts in vitro.

Copyright © 2020 Elsevier B.V. and Société Française de Biochimie et Biologie Moléculaire (SFBBM). All rights reserved.

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Funding

European Commission
ALGAE4A-B - Development of Microalgae-based novel high added-value products for the Cosmetic and Aquaculture industry 691102