Effect of Surface Chemical Functionalities on Collagen Deposition by Primary Human Dermal Fibroblasts

被引:31
作者
Bachhuka, Akash [1 ]
Hayball, John [3 ,4 ]
Smith, Louise E. [1 ,2 ]
Vasilev, K. [1 ,2 ]
机构
[1] Univ S Australia, Mawson Inst, Adelaide, SA 5095, Australia
[2] Univ S Australia, Sch Engn, Adelaide, SA 5095, Australia
[3] Univ S Australia, Sch Pharm & Med Sci, Sansom Inst, Expt Therapeut Lab, Adelaide, SA 5000, Australia
[4] Univ S Australia, Sch Pharm & Med Sci, Hanson Inst, Adelaide, SA 5000, Australia
关键词
plasma polymerization; surface chemistry; collagen I; collagen III; fibroblasts; SELF-ASSEMBLED MONOLAYERS; IN-VITRO; MACROSCOPIC KINETICS; PLASMA; RESPONSES; ADHESION; PERSPECTIVE; GRADIENTS; CHEMISTRY; COATINGS;
D O I
10.1021/acsami.5b08249
中图分类号
TB3 [工程材料学];
学科分类号
082905 [生物质能源与材料];
摘要
Surface modification has been identified as an important technique that could improve the response of the body to implanted medical devices. Collagen production by fibroblasts is known to play a vital role in wound healing and device fibrous encapsulation. However, how surface chemistry affects collagen I and III deposition by these cells has not been systematically studied. Here, we report how surface chemistry influences the deposition of collagen I and III by primary human dermal fibroblasts. Amine (NH3), carboxyl acid (COOH), and hydrocarbon (CH3) surfaces were generated by plasma deposition. This is a practically relevant tool to deposit a functional coating on any type of substrate material. We show that fibroblasts adhere better and proliferate faster on amine-rich surfaces. In addition, the initial collagen I and III production is greater on this type of coating. These data indicates that surface modification can be a promising route for modulating the rate and level of fibrous encapsulation and may be useful in informing the design of implantable biomedical devices to produce more predictable clinical outcomes.
引用
收藏
页码:23767 / 23775
页数:9
相关论文
共 58 条
[1]
STUDY ON THE PREVENTION OF SURFACE-INDUCED PLATELET ACTIVATION BY ALBUMIN COATING [J].
AMIJI, M ;
PARK, H ;
PARK, K .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1992, 3 (05) :375-388
[2]
Inflammatory response to implants [J].
Anderson, J.M. .
ASAIO Transactions, 1988, 34 (02) :101-107
[3]
Foreign body reaction to biomaterials [J].
Anderson, James M. ;
Rodriguez, Analiz ;
Chang, David T. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :86-100
[4]
Biological responses to materials [J].
Anderson, JM .
ANNUAL REVIEW OF MATERIALS RESEARCH, 2001, 31 :81-110
[5]
Monocyte, macrophage and foreign body giant cell interactions with molecularly engineered surfaces [J].
Anderson, JM ;
Defife, K ;
Mcnally, A ;
Collier, T ;
Jenney, C .
JOURNAL OF MATERIALS SCIENCE-MATERIALS IN MEDICINE, 1999, 10 (10-11) :579-588
[6]
Hybrid core/shell microparticles and their use for understanding biological processes [J].
Bachhuka, Akash ;
Christo, Susan N. ;
Cavallaro, Alex ;
Diener, Kerrilyn R. ;
Mierczynska, Agnieszka ;
Smith, Louise E. ;
Marian, Romeo ;
Manavis, Jim ;
Hayball, John D. ;
Vasilev, Krasimir .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2015, 457 :9-17
[7]
Bridges Amanda W, 2008, J Diabetes Sci Technol, V2, P984
[8]
Adsorption of immunoglobulin G to plasma-co-polymer surfaces of acrylic acid and 1,7-octadiene [J].
Bullett, NA ;
Whittle, JD ;
Short, RD ;
Douglas, CWI .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (07) :1546-1553
[9]
Kinetics of implant-induced inflammatory angiogenesis in abdominal muscle wall in mice [J].
Castro, Pollyana R. ;
Marques, Suzane M. ;
Campos, Paula P. ;
Cardoso, Cibele C. ;
Sampaio, Fernanda P. ;
Ferreira, Monica A. N. D. ;
Andrade, Silvia P. .
MICROVASCULAR RESEARCH, 2012, 84 (01) :9-15
[10]
The Scar-in-a-Jar: studying potential antifibrotic compounds from the epigenetic to extracellular level in a single well [J].
Chen, C. Z. C. ;
Peng, Y. X. ;
Wang, Z. B. ;
Fish, P. V. ;
Kaar, J. L. ;
Koepsel, R. R. ;
Russell, A. J. ;
Lareu, R. R. ;
Raghunath, M. .
BRITISH JOURNAL OF PHARMACOLOGY, 2009, 158 (05) :1196-1209