DOCSLIB.ORG

Differentiation of Human Dermal Fibroblasts and Applications in Tissue Engineering

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Differentiation of Human Dermal Fibroblasts and Applications in Tissue Engineering LINKÖPING UNIVERSITY MEDICAL DISSERTATIONS NO. 1202 DIFFERENTIATION OF HUMAN DERMAL FIBROBLASTS AND APPLICATIONS IN TISSUE ENGINEERING Pehr Sommar Division of Surgery Department of Clinical and Experimental Medicine Faculty of Health Sciences SE-581 85 Linköping, Sweden 2010 Published papers are reprinted with permission from the publisher. Printed by LiU-Tryck, Linköping, Sweden, 2010 © Pehr Sommar Cover by Pehr Sommar and Johan PE Junker Photos by Pehr Sommar, Figure 5; Sofia Pettersson Illustrations by Pehr Sommar and Kalle Lundgren ISBN 978-91-7393-326-1 ISSN 0345-0082 To Marie and Ingrid SUPERVISOR Gunnar Kratz, Professor Laboratory for Reconstructive Plastic Surgery Department of Plastic Surgery, Hand Surgery and Burns Department of Clinical and Experimental Medicine Linköping University, Sweden CO-SUPERVISOR Thomas Hansson, MD, PhD Department of Plastic Surgery, Hand Surgery and Burns University Hospital, Linköping, Sweden OPPONENT Anders Lindahl, Professor Institute of Biomedicine Department of Clinical Chemistry and Transfusion Medicine Sahlgrenska University Hospital, Gothenburg, Sweden COMMITTEE BOARD Sven Hammarström, Professor Division of Cell Biology Department of Clinical and Experimental Medicine Linköping University, Sweden Per Wretenberg, MD, PhD Department of Molecular Medicine and Surgery Section of Orthopaedics and Sports Medicine Karolinska Institute Karolinska University Hospital, Stockholm, Sweden Avni Abdiu, MD, PhD Department of Plastic Surgery, Hand Surgery and Burns University Hospital, Linköping, Sweden ABSTRACT Tissue engineering applies principles of biology and engineering to the development of functional substitutes for damaged or lost tissues. Tools for the neo-generation of tissue in tissue engineering research include cells, biomaterials and soluble factors. One main obstacle in tissue engineering is the limited availability of autologous tissue specific progenitor cells. This has led to interest into using autologous cells with stem cell plasticity. Bone marrow derived stem cells were the first adult stem cells shown to have multilineage potential. Since, several reports have been published indicating that cells from other tissues; fat, muscle, connective tissue e.g., possess potential to differentiate into lineages distinct from their tissue of origin. The optimal cell type for use in tissue engineering applications should be easy to obtain, cultivate and store. The human dermal fibroblast is an easily accessible cell source, which after routine cell expansion gives a substantial cell yield from a small skin biopsy. Hence, the dermal fibroblast could be a suitable cell source for tissue engineering applications. The main aim of this thesis was to investigate the differentiation capacity of human dermal fibroblasts, and their possible applications in bone and cartilage tissue engineering applications. Human dermal fibroblasts were shown to differentiate towards adipogenic, chondrogenic, and osteogenic phenotypes upon subjection to specific induction media. Differentiation was seen both in unrefined primary cultures and in clonal populations (paper I). Fibroblasts could be used to create three-dimensional cartilage- and bone like tissue when grown in vitro on gelatin microcarriers in combination with platelet rich plasma (paper II). 4 weeks after in vivo implantation of osteogenic induced fibroblasts into a fracture model in athymic rats, dense cell clusters and viable human cells were found in the gaps, but no visible healing of defects as determined by CT-scanning (paper III). After the induction towards adipogenic, chondrogenic, endotheliogenic and osteogenic lineages, gene expression analysis by microarray and quantitative real-time-PCR found several master regulatory genes important for lineage commitment, as well as phenotypically relevant genes regulated as compared to reference cultures (paper IV). In conclusion, results obtained in this thesis suggest an inherent ability for controllable phenotype alteration of human dermal fibroblasts in vitro. We conclude that dermal fibroblasts could be induced towards adipogenic, chondrogenic, endotheliogenic or osteogenic novel phenotypes, which suggest a genetic readiness of differentiated fibroblasts for lineage- specific biological functionality, indicating that human dermal fibroblasts might be a suitable cell source in tissue engineering applications. TABLE OF CONTENTS INTRODUCTION ................................................................................................................................................. 1 TISSUE ENGINEERING................................................................................................................................... 1 CELLS IN TISSUE ENGINEERING ................................................................................................................. 1 Stem cells and cellular differentiation ........................................................................................................... 2 Embryonic stem cells (ESCs) ......................................................................................................................... 3 Adult stem cells (ASCs).................................................................................................................................. 4 Induced pluripotent stem cells (iPSCs) .......................................................................................................... 5 Dermal fibroblasts ......................................................................................................................................... 6 BIOMATERIALS .............................................................................................................................................. 7 SOLUBLE FACTORS ....................................................................................................................................... 8 TISSUE ENGINEERING APPLICATIONS ..................................................................................................... 8 Tissue engineering of cartilage ..................................................................................................................... 8 Tissue engineering of bone ............................................................................................................................ 9 Clinical applications of tissue engineering ................................................................................................. 10 ADIPOSE TISSUE ........................................................................................................................................... 11 Histological and physiological features of adipose tissue ........................................................................... 11 Regulators of adipogenesis .......................................................................................................................... 11 Adipogenic induction factors ....................................................................................................................... 12 CARTILAGE TISSUE ..................................................................................................................................... 13 Histological and molecular features of cartilage ........................................................................................ 13 Regulators of chondrogenesis ..................................................................................................................... 15 Chondrogenic induction factors .................................................................................................................. 16 BONE TISSUE ................................................................................................................................................. 17 Histological and physiological features of bone ......................................................................................... 17 Regulators of osteogenesis .......................................................................................................................... 18 Osteogenic induction factors ....................................................................................................................... 19 ENDOTHELIAL CELLS ................................................................................................................................. 20 Histological and physiological features of the endothelium ........................................................................ 20 Regulators of endotheliogenesis .................................................................................................................. 21 Endothelial induction factors ...................................................................................................................... 22 AIMS .................................................................................................................................................................... 23 MATERIALS AND METHODS ....................................................................................................................... 25 ETHICAL PERMISSION ................................................................................................................................ 25 CELL HARVEST AND INDUCTION ............................................................................................................ 25 Fibroblasts ..................................................................................................................................................
Load more

Recommended publications
  • Mesenchymal Stromal Cells and Fibroblasts Christine Ulrich1, Melanie L
    Scienc e e & su s E i n T g f i o n Journal of Ulrich et al. J Tissue Sci Eng 2012, 3:1 l e e a r n i r n DOI: 10.4172/2157-7552.1000e109 u g o J ISSN: 2157-7552 Tissue Science & Engineering Editorial Open Access Mesenchymal Stromal Cells and Fibroblasts Christine Ulrich1, Melanie L. Hart1,2, Bernd Rolauffs3, Harald Abele4, Marco Götze5, Karin Benz6 and Wilhelm K. Aicher1,5* 1Center for Regenerative Biology and Medicine, University of Tübingen, Germany 2Department of Anesthesiology and Intensive Care, University of Tübingen Hospital, Tübingen, Germany 3BGU Trauma Center, Tübingen, Germany 4Department of Obstetrics and Gynaecology, UKT, University of Tübingen Hospital, Tübingen,Germany 5Department of Orthopaedic Surgery, University of Tübingen Hospital, Tübingen, Germany 6Department of Cell Biology, Regenerative Medicine II, NMI at University of Tübingen, Reutlingen, Germany Summary Adult mesenchymal stromal cells (MSC), also referred to as mesenchymal stem cells, were detected almost half a century ago in bone marrow and have been studied intensively in the last decade. Different aspects of MSC biology were explored and published. Studies pointed to their localization in different organs during development and in adulthood and described their characteristics in experimental or clinical investigations. Despite intensive research in the field and in sharp contrast to hematopoietic stem cells (HSC), it has become more and more clear that MSC lack a unique cell surface marker. MSC not only share cell surface markers with other types of cells, they also share many features with pericytes and fibroblasts, including their capability to differentiate into, for instance, osteoblasts or adipocytes.
    [Show full text]
  • Effects of Collagen-Derived Bioactive Peptides and Natural Antioxidant
    www.nature.com/scientificreports OPEN Efects of collagen-derived bioactive peptides and natural antioxidant compounds on Received: 29 December 2017 Accepted: 19 June 2018 proliferation and matrix protein Published: xx xx xxxx synthesis by cultured normal human dermal fbroblasts Suzanne Edgar1, Blake Hopley1, Licia Genovese2, Sara Sibilla2, David Laight1 & Janis Shute1 Nutraceuticals containing collagen peptides, vitamins, minerals and antioxidants are innovative functional food supplements that have been clinically shown to have positive efects on skin hydration and elasticity in vivo. In this study, we investigated the interactions between collagen peptides (0.3–8 kDa) and other constituents present in liquid collagen-based nutraceuticals on normal primary dermal fbroblast function in a novel, physiologically relevant, cell culture model crowded with macromolecular dextran sulphate. Collagen peptides signifcantly increased fbroblast elastin synthesis, while signifcantly inhibiting release of MMP-1 and MMP-3 and elastin degradation. The positive efects of the collagen peptides on these responses and on fbroblast proliferation were enhanced in the presence of the antioxidant constituents of the products. These data provide a scientifc, cell-based, rationale for the positive efects of these collagen-based nutraceutical supplements on skin properties, suggesting that enhanced formation of stable dermal fbroblast-derived extracellular matrices may follow their oral consumption. Te biophysical properties of the skin are determined by the interactions between cells, cytokines and growth fac- tors within a network of extracellular matrix (ECM) proteins1. Te fbril-forming collagen type I is the predomi- nant collagen in the skin where it accounts for 90% of the total and plays a major role in structural organisation, integrity and strength2.
    [Show full text]
  • Cross-Tissue, Single-Cell Stromal Atlas Identifies Shared Pathological Fibroblast Phenotypes In
    bioRxiv preprint doi: https://doi.org/10.1101/2021.01.11.426253; this version posted January 12, 2021. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Cross-tissue, single-cell stromal atlas identifies shared pathological fibroblast phenotypes in 2 four chronic inflammatory diseases 3 Ilya Korsunsky1-5,15, Kevin Wei1,15, Mathilde Pohin6,15, Edy Y. Kim7,8,15, Francesca Barone9,15, Joyce 4 B. Kang1-5, Matthias Friedrich6, Jason Turner9, Saba Nayar9,10, Benjamin A. Fisher9,10, Karim Raza9,, 5 Jennifer L. Marshall9, Adam P. Croft9, Lynette M. Sholl11, Marina Vivero11, Ivan O. Rosas12, Simon J. 6 Bowman9,10, Mark Coles6, Andreas P. Frei13, Kara Lassen13, Andrew Filer9,10, Fiona Powrie6,16,*, 7 Christopher D. Buckley9,10,16,*, Michael B. Brenner1,7,16,*, Soumya Raychaudhuri1-5,14,16,17,* 8 1Division of Rheumatology, Inflammation and Immunity, Brigham and Women’s Hospital and Harvard Medical School, 9 Boston, MA, USA. 10 2Center for Data Sciences, Brigham and Women’s Hospital, Boston, MA, USA. 11 3Division of Genetics, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA. 12 4Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. 13 5Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. 14 6Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, 15 University of Oxford, Oxford OX3 7FY, United Kingdom 16 7Harvard Medical School, Boston, MA 02115, USA 17 8Division of Pulmonary and Critical Care Medicine, Brigham and Women’s Hospital, Boston, MA 02115, USA 18 9Rheumatology Research Group, Institute for Inflammation and Ageing, College of Medical and Dental Sciences, 19 University of Birmingham, Queen Elizabeth Hospital, Birmingham, B15 2WD, UK.
    [Show full text]
  • Human Dermal Fibroblast Manual
    ZenBio, Inc. Human Dermal Fibroblast Manual INSTRUCTIONAL MANUAL ZBM0023.05 SHIPPING CONDITIONS Human Adult or Neonatal Dermal Fibroblast Cells Orders are delivered via Federal Express courier. All US and Canada orders are shipped via Federal Express Priority service and are usually received the next day. International orders are usually received in 3-4 days. Must be processed upon shipment receipt. STORAGE CONDITIONS Media: Short Term (30 days): 4°C 6 months -20°C Cells: Frozen: Vapor phase liquid nitrogen Live Plated: 37°C incubator All Zen-Bio Inc products are for research use only. Not approved for human or veterinary use or for use in diagnostic or clinical procedures. ORDERING INFORMATION AND TECHNICAL SERVICES ZenBio, Inc. 3200 East NC-54 Suite 100 PO Box 13888 Research Triangle Park, NC 27709 U.S.A. Telephone (919) 547-0692 Facsimile (FAX) (919) 547-0693 Toll free (continental US only) 1-866-ADIPOSE 1-(866)-234-7673 Electronic mail (e-mail) [email protected] World Wide Web http://www.zenbio.com THIS MANUAL IS SUITABLE FOR USE WITH THE FOLLOWING PRODUCTS: DF-F HUMAN DERMAL FIBROBLASTS DFN-F HUMAN NEONATAL DERMAL FIBROBLASTS DF-F-PS HUMAN DERMAL FIBROBLASTS FROM PSORIASIS DONOR DF-D-F HUMAN DERMAL FIBROBLASTS FROM TYPE 2 DIABETIC DONOR DF-1, DF-1-PRF DERMAL FIBROBLAST MEDIUM, - PHENOL RED FREE DFM-100 DERMAL FIBROBLAST CRYOPRESERVATION MEDIUM RV. 04.2016 Page 1 of 7 ZenBio, Inc. CONTENTS PAGE # Introduction/Precautions/Warranty 3 Catalog Items 4 Media Compositions 4 Plating and Expansion of Cryopreserved Cells 5 Frequently Asked Questions 6 Pathogen Testing 7 RV.
    [Show full text]
  • Scientists Make Stem Cells That Are Accepted by the Ethical Community
    Scientists Make Stem Cells that Are Accepted by the Ethical Community By Colby Chiang '10 In November, two teams of scientists published methods of generating embryonic-like stem cells without destroying an embryo, a finding that could quell the ethical controversy surrounding stem cell research. The two independent research teams, headed by James Thomson of the University of Wisconsin-Madison and Shinya Yamanaka of Kyoto University in Japan, developed methods to induce pluripotency, the quality that allows stem cells to develop into any kind of body cells. The “induced pluripotent stem cells” (iPS cells) can then be differentiated into any of the body's 220 somatic cell types. Until now, the only way to acquire pluripotent cells was to harvest them from a fertilized embryo, destroying the embryo in the process. The technique to reprogram the cells is surprisingly simple. Scientists must only add four genes, which in turn activate a cascade of other factors that rewind cell development. To introduce the genes into the cells, they use retrovirus vectors, which have the ability to insert short sequences into DNA. Once the relevant DNA is inducted into the cell, it activates genetic pathways that revert the cell to its pluripotent state. This discovery in human cells was preceded by similar findings in July of 2006, when Shinya Yamanaka created iPS cell lines from the tail cells of mice (1). Now Yamanaka's team has managed to apply the same technique to human cells, even using the same set of genes. The group has generated iPS cell lines both from the facial dermal fibroblast cells of a 36-year-old woman and from the connective tissue of a 69-year-old man.
    [Show full text]
  • Oxidative Stress and Human Skin Connective Tissue Aging
    cosmetics Review Oxidative Stress and Human Skin Connective Tissue Aging Yidong Tu 1 and Taihao Quan 2,* 1 Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, MO 63110, USA; [email protected] 2 Department of Dermatology, University of Michigan Medical School, Ann Arbor, MI 48109, USA * Correspondence: [email protected]; Tel.: +1-734-165-2403; Fax: +1-734-647-0076 Academic Editor: Enzo Berardesca Received: 14 June 2016; Accepted: 2 August 2016; Published: 5 August 2016 Abstract: Everyone desires healthy and beautiful-looking skin. However, as we age, our skin becomes old due to physiological changes. Reactive oxygen species (ROS) is an important pathogenic factor involved in human aging. Human skin is exposed to ROS generated from both extrinsic sources such as as ultraviolet (UV) light from the sun, and intrinsic sources such as endogenous oxidative metabolism. ROS-mediated oxidative stress damages the collagen-rich extracellular matrix (ECM), the hallmark of skin connective tissue aging. Damage to dermal collagenous ECM weakens the skin’s structural integrity and creates an aberrant tissue microenvironment that promotes age-related skin disorders, such as impaired wound healing and skin cancer development. Here, we review recent advances in our understanding of ROS/oxidative stress and skin connective tissue aging. Keywords: ROS; oxidative stress; MMPs; TGF-β; CCN1; skin aging; fibroblasts; ECM; collagen 1. Introduction Skin is the largest organ of the human body and changes in the skin are among the most visible signs of an aged appearance. The skin’s appearance is central to the social and visual experience, and it has significant emotional and psychological impacts on our life quality.
    [Show full text]
  • Fibroblasts from the Human Skin Dermo-Hypodermal Junction Are
    cells Article Fibroblasts from the Human Skin Dermo-Hypodermal Junction are Distinct from Dermal Papillary and Reticular Fibroblasts and from Mesenchymal Stem Cells and Exhibit a Specific Molecular Profile Related to Extracellular Matrix Organization and Modeling Valérie Haydont 1,*, Véronique Neiveyans 1, Philippe Perez 1, Élodie Busson 2, 2 1, 3,4,5,6, , Jean-Jacques Lataillade , Daniel Asselineau y and Nicolas O. Fortunel y * 1 Advanced Research, L’Oréal Research and Innovation, 93600 Aulnay-sous-Bois, France; [email protected] (V.N.); [email protected] (P.P.); [email protected] (D.A.) 2 Department of Medical and Surgical Assistance to the Armed Forces, French Forces Biomedical Research Institute (IRBA), 91223 CEDEX Brétigny sur Orge, France; [email protected] (É.B.); [email protected] (J.-J.L.) 3 Laboratoire de Génomique et Radiobiologie de la Kératinopoïèse, Institut de Biologie François Jacob, CEA/DRF/IRCM, 91000 Evry, France 4 INSERM U967, 92260 Fontenay-aux-Roses, France 5 Université Paris-Diderot, 75013 Paris 7, France 6 Université Paris-Saclay, 78140 Paris 11, France * Correspondence: [email protected] (V.H.); [email protected] (N.O.F.); Tel.: +33-1-48-68-96-00 (V.H.); +33-1-60-87-34-92 or +33-1-60-87-34-98 (N.O.F.) These authors contributed equally to the work. y Received: 15 December 2019; Accepted: 24 January 2020; Published: 5 February 2020 Abstract: Human skin dermis contains fibroblast subpopulations in which characterization is crucial due to their roles in extracellular matrix (ECM) biology.
    [Show full text]
  • Type VI Collagen Regulates Dermal Matrix Assembly and Fibroblast Motility
    View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by LSBU Research Open Accepted Article Preview: Published ahead of advance online publication www.jidonline.org Type VI Collagen Regulates Dermal Matrix Assembly and Fibroblast Motility Georgios Theocharidis, Zoe Drymoussi, Alexander P Kao, Asa H Barber, David A Lee, Kristin M Braun, John T Connelly Cite this article as: Georgios Theocharidis, Zoe Drymoussi, Alexander P Kao, Asa H Barber, David A Lee, Kristin M Braun, John T Connelly, Type VI Collagen Regulates Dermal Matrix Assembly and Fibroblast Motility, Journal of Investigative Dermatology accepted article preview 9 September 2015; doi: 10.1038/jid.2015.352. This is a PDF file of an unedited peer-reviewed manuscript that has been accepted for publication. NPG are providing this early version of the manuscript as a service to our customers. The manuscript will undergo copyediting, typesetting and a proof review before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers apply. Received 31 March 2015; revised 16 July 2015; accepted 17 August 2015; Accepted article preview online 9 September 2015 © 2015 The Society for Investigative Dermatology Type VI collagen regulates dermal matrix assembly and fibroblast motility Georgios Theocharidis1, Zoe Drymoussi1, Alexander P. Kao2, Asa H. Barber2,3 David A. Lee2, Kristin M. Braun1, John T. Connelly1* 1. Centre for Cell Biology and Cutaneous Research, Barts and the London School of Medicine and Dentistry, Queen Mary, University of London. 2. Institute of Bioengineering, School of Engineering and Materials Science, Queen Mary, University of London.
    [Show full text]
  • Human Adipocyte Conditioned Medium Promotes in Vitro Fibroblast Conversion to Myofibroblasts
    www.nature.com/scientificreports OPEN Human Adipocyte Conditioned Medium Promotes In Vitro Fibroblast Conversion to Myofbroblasts Mariam Y. El-Hattab1, Yoshiaki Nagumo1,2, Francoise A. Gourronc3, Aloysius J. Klingelhutz3,4, James A. Ankrum1,4 ✉ & Edward A. Sander1,5 ✉ Adipocytes and adipose tissue derived cells have been investigated for their potential to contribute to the wound healing process. However, the details of how these cells interact with other essential cell types, such as myofbroblasts/fbroblasts, remain unclear. Using a novel in-vitro 3D human adipocyte/ pre-adipocyte spheroid model, we investigated whether adipocytes and their precursors (pre- adipocytes) secrete factors that afect human dermal fbroblast behavior. We found that both adipocyte and pre-adipocyte conditioned medium induced the migration of fbroblasts, but only adipocyte conditioned medium induced fbroblast diferentiation into a highly contractile, collagen producing myofbroblast phenotype. Furthermore, adipocyte mediated myofbroblast induction occurred through a TGF-β independent mechanism. Our fndings contribute to a better understanding on the involvement of adipose tissue in wound healing, and may help to uncover and develop fat-related wound healing treatments. Impaired wound healing impacts millions of people in the US annually with estimated treatment and manage- ment costs totaling $20 billion dollars1. Problems in the healing process can arise from multiple factors during any stage of wound healing. Examples include exposure to elevated growth factors and cytokines during a prolonged period of infammation2–4, increased mechanical tension that drives excessive matrix deposition during tissue formation5–7, and altered rates of matrix degradation and remodeling during the remodeling phase of wound healing5,8. Treatment options include various types of dressings, negative-pressure therapies, laser treatments, and the use of corticosteroids, growth factors, drugs and other cellular products1,9,10.
    [Show full text]
  • SOP for Human Dermal Fibroblast Isolation
    SOP for Human Dermal Fibroblast Isolation 6mm Punch Biopsy from Arm Placed immediately into 15 cc conical containing DMEM with 1% pen-strep. 1. In sterile hood transfer the skin sample to the 15 mL conical with waiting 1mL digestion media*. Cap the tube tightly and place in 37C tissue culture incubator overnight. 2. The next day vortex for 20 seconds to disrupt the skin—observe separation of the epidermis, and disintegration of the dermis. 3. Wipe off the outside of the conical tube with alcohol to sterilize it before entering hood. 4. In a sterile tissue culture hood, add 7ml of fibroblast culture media** to the conical tube, pipette up and down to mix 2-3 times and then plate entire contents in a T75 tissue culture flask. 5. Incubate for 3 days without touching the flask to allow cells to settle/adhere—check at 72 hours to assess whether fibroblasts are starting to grow. 6. On day 6-7 the culture will have started to turn yellow or will be at risk of drying out— in this case, add 7 mL more of fibroblast culture media (but with 10% FBS DMEM, rather than 20% FBS). 7. When 80% confluent, passage 1:3 using 0.25% trypsin/EDTA. Upon passaging, FBS can be reduced from 20% to 10%. 8. A small aliquot should be taken for mycoplasma testing by PCR (see mycoplasma SOP) 9. Begin reprogramming at passage 3 and freeze down backup vials for liquid nitrogen storage. Digestion media* (per Andrea Bujor, MD): 8 mL FBS (final conc=20% FBS) 32 mL DMEM (hi glucose) 100 mg Collagenase type I, 0.25% final.
    [Show full text]
  • Identification of Regulators of the Myofibroblast Phenotype of Primary
    www.nature.com/scientificreports OPEN Identifcation of regulators of the myofbroblast phenotype of primary dermal fbroblasts from Received: 18 June 2018 Accepted: 18 February 2019 early difuse systemic sclerosis Published: xx xx xxxx patients Loubna Chadli1, Britt Sotthewes1, Kejie Li2, Stefan N. Andersen1, Ellen Cahir- McFarland2, Marc Cheung1, Patrick Cullen2, Annemarie Dorjée3, Jeska K. de Vries- Bouwstra3, Tom W. J. Huizinga3, David F. Fischer1, Jeroen DeGroot 1, Joanne L. Viney2, Timothy S. Zheng2, Jamil Aarbiou1 & Agnes Gardet2 Systemic sclerosis (SSc or scleroderma) is an auto-immune disease characterized by skin fbrosis. While primary cells from patients are considered as a unique resource to better understand human disease biology, the efect of in vitro culture on these cells and their evaluation as a platform to identify disease regulators remain poorly characterized. The goal of our studies was to provide insights into the utility of SSc dermal fbroblast primary cells for therapeutic target discovery. The disease phenotypes of freshly isolated and in vitro cultured SSc dermal fbroblasts were characterized using whole transcriptome profling, alpha smooth muscle actin (ASMA) expression and cell impedance. SSc dermal fbroblasts retained most of the molecular disease phenotype upon in vitro culture for at least four cell culture passages (approximatively 10 cell doublings). We validated an RNA interference high throughput assay that successfully identifed genes afecting the myofbroblast phenotype of SSc skin fbroblasts. These genes included MKL1, RHOA and LOXL2 that were previously proposed as therapeutic anti-fbrotic target, and ITGA5, that has been less studied in fbrosis biology and may be a novel potential modifer of SSc fbroblast biology.
    [Show full text]
  • Primary Human Fibroblasts in Culture Switch to a Myofibroblast-Like
    cells Article Primary Human Fibroblasts in Culture Switch to a Myofibroblast-Like Phenotype Independently of TGF Beta Ulrike Baranyi 1, Birgitta Winter 1, Alfred Gugerell 2,3 , Balazs Hegedus 4, Christine Brostjan 2, Günther Laufer 5 and Barbara Messner 1,* 1 Cardiac Surgery Research Laboratory, Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria 2 Department of Surgery, Medical University of Vienna, 1090 Vienna, Austria 3 Department of Cardiology, Medical University of Vienna, 1090 Vienna, Austria 4 Division of Thoracic Surgery, Department of Surgery, Comprehensive Cancer Center Vienna, Medical University of Vienna, 1090 Vienna, Austria 5 Department of Cardiac Surgery, Medical University of Vienna, 1090 Vienna, Austria * Correspondence: [email protected]; Tel.: +43-1-40400-69490; Fax: +43-1-40400-67820 Received: 22 March 2019; Accepted: 9 July 2019; Published: 13 July 2019 Abstract: Fibroblasts are the prevalent cell type and main source for extracellular matrix (ECM) in connective tissue. Depending on their origin, fibroblasts play a central role in non-pathological tissue remodeling and disease like fibrosis. This study examined the effect of established culture conditions of primary human fibroblasts, from different origins on the myofibroblast-like phenotype formation. We isolated primary human fibroblasts from aortic adventitia, lung, juvenile- and adult skin and investigated the expression levels of CD90, alpha smooth muscle actin (αSMA) and procollagen I under different concentrations of fetal calf serum (FCS) and ascorbic acid (AA) in culture media by immunoblot and immunofluorescence assays. Furthermore, we determined the viability using XTT and migration/wound healing in scratch assays. Collagen 1 secretion was quantified by specific ELISA.
    [Show full text]