Tuning cellular responses to BMP-2 with material surfaces. (February 2016)
- Record Type:
- Journal Article
- Title:
- Tuning cellular responses to BMP-2 with material surfaces. (February 2016)
- Main Title:
- Tuning cellular responses to BMP-2 with material surfaces
- Authors:
- Migliorini, Elisa
Valat, Anne
Picart, Catherine
Cavalcanti-Adam, Elisabetta Ada - Abstract:
- Graphical abstract: Highlights: New material surfaces are tailored to provide physical and chemical cues that regulate BMP-2 activity. Physical entrapment or chemical binding of BMP-2 on material surfaces modulate the temporal activity of BMP-2. Surface patterning at different length scales allows the spatial control of BMP-2. Material surfaces copresenting BMP-2 together with extracellular matrix components are suitable platforms to study cells adhesion and response to external stimuli. ABSTRACT: Bone morphogenetic protein 2 (BMP-2) has been known for decades as a strong osteoinductive factor and for clinical applications is combined solely with collagen as carrier material. The growing concerns regarding side effects and the importance of BMP-2 in several developmental and physiological processes have raised the need to improve the design of materials by controlling BMP-2 presentation. Inspired by the natural cell environment, new material surfaces have been engineered and tailored to provide both physical and chemical cues that regulate BMP-2 activity. Here we describe surfaces designed to present BMP-2 to cells in a spatially and temporally controlled manner. This is achieved by trapping BMP-2 using physicochemical interactions, either covalently grafted or combined with other extracellular matrix components. In the near future, we anticipate that material science and biology will integrate and further develop tools for in vitro studies and potentially bring some of themGraphical abstract: Highlights: New material surfaces are tailored to provide physical and chemical cues that regulate BMP-2 activity. Physical entrapment or chemical binding of BMP-2 on material surfaces modulate the temporal activity of BMP-2. Surface patterning at different length scales allows the spatial control of BMP-2. Material surfaces copresenting BMP-2 together with extracellular matrix components are suitable platforms to study cells adhesion and response to external stimuli. ABSTRACT: Bone morphogenetic protein 2 (BMP-2) has been known for decades as a strong osteoinductive factor and for clinical applications is combined solely with collagen as carrier material. The growing concerns regarding side effects and the importance of BMP-2 in several developmental and physiological processes have raised the need to improve the design of materials by controlling BMP-2 presentation. Inspired by the natural cell environment, new material surfaces have been engineered and tailored to provide both physical and chemical cues that regulate BMP-2 activity. Here we describe surfaces designed to present BMP-2 to cells in a spatially and temporally controlled manner. This is achieved by trapping BMP-2 using physicochemical interactions, either covalently grafted or combined with other extracellular matrix components. In the near future, we anticipate that material science and biology will integrate and further develop tools for in vitro studies and potentially bring some of them toward in vivo applications. … (more)
- Is Part Of:
- Cytokine & growth factor reviews. Volume 27(2016)
- Journal:
- Cytokine & growth factor reviews
- Issue:
- Volume 27(2016)
- Issue Display:
- Volume 27, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 27
- Issue:
- 2016
- Issue Sort Value:
- 2016-0027-2016-0000
- Page Start:
- 43
- Page End:
- 54
- Publication Date:
- 2016-02
- Subjects:
- 2(3)D two(three) dimensional -- ALP alkaline phosphatase -- BMP-2 bone morphogenetic protein -- b-BMP2 biotinylated BMP-2 -- rhBMP-2 recombinant human BMP-2 -- BMPRI(II) BMP type I (II) receptors -- Cdc42 cell division control protein 42 homolog -- CS chondroitin sulfate -- C2C12 mouse myoblast cell line -- ECM extracellular matrix -- ELISA enzyme-linked immunosorbent assay -- ERK extracellular signal-regulated kinases -- FAK focal adhesion kinase -- FN fibronectin -- GAGs glycosaminoglycans -- GTPase guanosine triphosphate hydrolase -- HA hyaluronic acid -- Hp heparin -- HS heparan sulfate -- Id-1 inhibitor of DNA binding 1 -- ILK integrin-linked kinase -- LbL layer-by-layer -- LIMK1 LIM domain kinase 1 -- MAPK mitogen-activated protein kinase -- PI3K phosphoinositide 3-kinase -- PLL poly-l-lysine -- RGD arginine, glycine, aspartic acid -- Rho ras homolog gene family -- ROCK rho-associated protein kinase -- SAM self assembly monolayer -- SAv streptavidin -- SMAD small mothers against decapentaplegic -- TGF-β transforming growth factor beta -- VEGFR vascular epidermal growth factor
BMP-2 -- Material surface -- Cell adhesion -- Growth factor immobilization -- BMP receptors -- Signaling
Cytokines -- Periodicals
571.84 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13596101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.cytogfr.2015.11.008 ↗
- Languages:
- English
- ISSNs:
- 1359-6101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3506.778500
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