Hemostatic properties and the role of cell receptor recognition in human hair keratin protein hydrogels

Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been in...

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Published in:Biomaterials Vol. 34; no. 11; pp. 2632 - 2640
Main Authors: Burnett, Luke R., Rahmany, Maria B., Richter, Jillian R., Aboushwareb, Tamer A., Eberli, Daniel, Ward, Catherine L., Orlando, Giuseppe, Hantgan, Roy R., Van Dyke, Mark E.
Format: Journal Article
Language:English
Published: Netherlands Elsevier Ltd 01.04.2013
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ISSN:0142-9612, 1878-5905, 1878-5905
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Abstract Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been inadequately described in terms of composition, structure, and cell-instructive characteristics. In this manuscript we describe and characterize a keratin-based biomaterial, demonstrate self-assembly of cross-linked hydrogels, investigate a cell-specific interaction that is dependent on the hydrogel structure and mediated by specific biomaterial–receptor interactions, and show one potential medical application that relies on receptor binding - the ability to achieve hemostasis in a lethal liver injury model. Keratin biomaterials represent a significant advance in biotechnology as they combine the compatibility of natural materials with the chemical flexibility of synthetic materials. These characteristics allow for a system that can be formulated into several varieties of cell-instructive biomaterials with potential uses in tissue engineering, regenerative medicine, drug and cell delivery, and trauma.
AbstractList Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been inadequately described in terms of composition, structure, and cell-instructive characteristics. In this manuscript we describe and characterize a keratin-based biomaterial, demonstrate self-assembly of cross-linked hydrogels, investigate a cell-specific interaction that is dependent on the hydrogel structure and mediated by specific biomaterial-receptor interactions, and show one potential medical application that relies on receptor binding - the ability to achieve hemostasis in a lethal liver injury model. Keratin biomaterials represent a significant advance in biotechnology as they combine the compatibility of natural materials with the chemical flexibility of synthetic materials. These characteristics allow for a system that can be formulated into several varieties of cell-instructive biomaterials with potential uses in tissue engineering, regenerative medicine, drug and cell delivery, and trauma.
Abstract Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been inadequately described in terms of composition, structure, and cell-instructive characteristics. In this manuscript we describe and characterize a keratin-based biomaterial, demonstrate self-assembly of cross-linked hydrogels, investigate a cell-specific interaction that is dependent on the hydrogel structure and mediated by specific biomaterial–receptor interactions, and show one potential medical application that relies on receptor binding - the ability to achieve hemostasis in a lethal liver injury model. Keratin biomaterials represent a significant advance in biotechnology as they combine the compatibility of natural materials with the chemical flexibility of synthetic materials. These characteristics allow for a system that can be formulated into several varieties of cell-instructive biomaterials with potential uses in tissue engineering, regenerative medicine, drug and cell delivery, and trauma.
Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been inadequately described in terms of composition, structure, and cell-instructive characteristics. In this manuscript we describe and characterize a keratin-based biomaterial, demonstrate self-assembly of cross-linked hydrogels, investigate a cell-specific interaction that is dependent on the hydrogel structure and mediated by specific biomaterial-receptor interactions, and show one potential medical application that relies on receptor binding - the ability to achieve hemostasis in a lethal liver injury model. Keratin biomaterials represent a significant advance in biotechnology as they combine the compatibility of natural materials with the chemical flexibility of synthetic materials. These characteristics allow for a system that can be formulated into several varieties of cell-instructive biomaterials with potential uses in tissue engineering, regenerative medicine, drug and cell delivery, and trauma.Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells and tissues to actively direct and sustain cellular behavior. Keratin biomaterials have the potential to achieve these goals but have been inadequately described in terms of composition, structure, and cell-instructive characteristics. In this manuscript we describe and characterize a keratin-based biomaterial, demonstrate self-assembly of cross-linked hydrogels, investigate a cell-specific interaction that is dependent on the hydrogel structure and mediated by specific biomaterial-receptor interactions, and show one potential medical application that relies on receptor binding - the ability to achieve hemostasis in a lethal liver injury model. Keratin biomaterials represent a significant advance in biotechnology as they combine the compatibility of natural materials with the chemical flexibility of synthetic materials. These characteristics allow for a system that can be formulated into several varieties of cell-instructive biomaterials with potential uses in tissue engineering, regenerative medicine, drug and cell delivery, and trauma.
Author Eberli, Daniel
Burnett, Luke R.
Rahmany, Maria B.
Aboushwareb, Tamer A.
Ward, Catherine L.
Orlando, Giuseppe
Richter, Jillian R.
Van Dyke, Mark E.
Hantgan, Roy R.
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  givenname: Luke R.
  surname: Burnett
  fullname: Burnett, Luke R.
  email: lburnett@wakehealth.edu
  organization: KeraNetics LLC, Winston Salem, NC, USA
– sequence: 2
  givenname: Maria B.
  surname: Rahmany
  fullname: Rahmany, Maria B.
  email: mbahawdo@wakehealth.edu
  organization: Department of Orthopaedic Surgery, Wake Forest University School of Medicine, USA
– sequence: 3
  givenname: Jillian R.
  surname: Richter
  fullname: Richter, Jillian R.
  email: jrichter@wakehealth.edu
  organization: Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, USA
– sequence: 4
  givenname: Tamer A.
  surname: Aboushwareb
  fullname: Aboushwareb, Tamer A.
  email: aboushwareb_tamer@allergan.com
  organization: Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, USA
– sequence: 5
  givenname: Daniel
  surname: Eberli
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  organization: Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, USA
– sequence: 6
  givenname: Catherine L.
  surname: Ward
  fullname: Ward, Catherine L.
  email: catward@wakehealth.edu
  organization: Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, USA
– sequence: 7
  givenname: Giuseppe
  surname: Orlando
  fullname: Orlando, Giuseppe
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  organization: Wake Forest Institute for Regenerative Medicine, Wake Forest University School of Medicine, USA
– sequence: 8
  givenname: Roy R.
  surname: Hantgan
  fullname: Hantgan, Roy R.
  email: rhantgan@wakehealth.edu
  organization: Department of Biochemistry, Wake Forest School of Medicine, USA
– sequence: 9
  givenname: Mark E.
  surname: Van Dyke
  fullname: Van Dyke, Mark E.
  email: mavandyk@wakehealth.edu, mvandyk5@vt.edu
  organization: Department of Orthopaedic Surgery, Wake Forest University School of Medicine, USA
BackLink https://www.ncbi.nlm.nih.gov/pubmed/23340195$$D View this record in MEDLINE/PubMed
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Keywords Keratin
Platelet
Biomaterial
Integrin
Hemostasis
Adhesion
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Snippet Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions with cells...
Abstract Driven by new discoveries in stem-cell biology and regenerative medicine, there is broad interest in biomaterials that go beyond basic interactions...
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SubjectTerms Adhesion
Advanced Basic Science
Animals
biocompatible materials
Biocompatible Materials - analysis
Biocompatible Materials - chemistry
Biomaterial
biotechnology
Blood Platelets - cytology
Blood Platelets - metabolism
Blotting, Western
Cell Adhesion
Colorimetry
crosslinking
Dentistry
drugs
Electrophoresis
Hair - chemistry
Hemostasis
Hemostatics - metabolism
Humans
hydrocolloids
Hydrogels - analysis
Hydrogels - chemistry
Integrin
Keratin
Keratins - analysis
Keratins - chemistry
liver
Mass Spectrometry
medicine
Microscopy, Confocal
Microscopy, Electron, Scanning
Platelet
Regenerative Medicine - methods
Rheology
Swine
tissue engineering
Tissue Engineering - methods
tissues
Title Hemostatic properties and the role of cell receptor recognition in human hair keratin protein hydrogels
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https://dx.doi.org/10.1016/j.biomaterials.2012.12.022
https://www.ncbi.nlm.nih.gov/pubmed/23340195
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Volume 34
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