Bacteria induced pH changes in tissue-engineered human skin detected non-invasively using Raman confocal spectroscopy

被引:37
作者
Bullock, Anthony J. [1 ]
Garcia, Marcela [2 ]
Shepherd, Joanna [3 ]
Rehman, Ihtesham [2 ]
Sheila, MacNeil [2 ]
机构
[1] Univ Sheffield, Mat Sci & Engn, Sheffield S3 7HQ, S Yorkshire, England
[2] Univ Sheffield, Kroto Res Inst, Dept Mat Sci & Engn, Sheffield, S Yorkshire, England
[3] Univ Sheffield, Sch Clin Dent, Sheffield, S Yorkshire, England
基金
欧盟地平线“2020”;
关键词
pH; skin; bacteria; tissue-engineered; PSEUDOMONAS-AERUGINOSA; EXTRACELLULAR PH; GRADIENTS; BIOFILMS; MODELS;
D O I
10.1080/05704928.2018.1558232
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Skin has a highly regulated pH environment of around pH 7.2 but with an acid barrier mantle of around pH 5.5. Trauma, inflammation, and infection are all thought to disrupt this pH environment but the lack of a non-invasive technique to measure pH within discrete locations within skin has hindered investigating what role pH plays in wound healing. In this study, a confocal Raman microspectroscopy method was used for measuring pH in a 3D tissue engineered model of human skin (TE-skin) and evaluated for its ability to detect changes in pH in response to wounding, inflammation and bacterial infection. The state of protonation of phosphate groups within the TE-skin was used to indicate pH in a non-destructive manner exploring depths of skin from the stratum corneum to 600 microns into the dermis. Deliberate wounding or inflammation (induced by IL-17) resulted in a loss of the acid mantle. Detailed scanning of TE-skin infected with Staphylococcus aureus or Pseudomonas aeruginosa revealed heterogeneous pH microenvironments ranging in size from 10 x 10 to 50 x 100 microns and ranging from pH 5 to 9. These microenvironments were not detected if an average pH for the TE-skin model was used.
引用
收藏
页码:158 / 171
页数:14
相关论文
共 34 条
[1]   Serum levels of TNF-α, IFN-γ, IL-6, IL-8, IL-12, IL-17 and IL-18 in patients with active psoriasis and correlation with disease severity [J].
Arican, O ;
Aral, M ;
Sasmaz, S ;
Ciragil, P .
MEDIATORS OF INFLAMMATION, 2005, (05) :273-279
[2]   3-DIMENSIONAL STRUCTURE OF THE ALKALINE PROTEASE OF PSEUDOMONAS-AERUGINOSA - A 2-DOMAIN PROTEIN WITH A CALCIUM-BINDING PARALLEL-BETA ROLL MOTIF [J].
BAUMANN, U ;
WU, S ;
FLAHERTY, KM ;
MCKAY, DB .
EMBO JOURNAL, 1993, 12 (09) :3357-3364
[3]   Tissue-engineered buccal mucosa for substitution urethroplasty [J].
Bhargava, S ;
Chapple, CR ;
Bullock, AJ ;
Layton, C ;
MacNeil, S .
BJU INTERNATIONAL, 2004, 93 (06) :807-811
[4]  
Bhargava S., 2003, BR J UROL, V91, P22
[5]   Raman spectroscopy in biomedicine - non-invasive in vitro analysis of cells and extracellular matrix components in tissues [J].
Brauchle, Eva ;
Schenke-Layland, Katja .
BIOTECHNOLOGY JOURNAL, 2013, 8 (03) :288-297
[6]   The effect of induced biphasic pulsed currents on re-epithelialization of a novel wound healing model [J].
Bullock, Anthony J. ;
Barker, Anthony T. ;
Coulton, Leslie ;
MacNeill, Shelia .
BIOELECTROMAGNETICS, 2007, 28 (01) :31-41
[7]   Development of autologous human dermal-epidermal composites based on sterilized human allodermis for clinical use [J].
Chakrabarty, KH ;
Dawson, RA ;
Harris, P ;
Layton, C ;
Babu, M ;
Gould, L ;
Phillips, J ;
Leigh, I ;
Green, C ;
Freedlander, E ;
Mac Neil, S .
BRITISH JOURNAL OF DERMATOLOGY, 1999, 141 (05) :811-823
[8]   Visual imaging of ion distribution in human epidermis [J].
Denda, M ;
Hosoi, J ;
Asida, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 272 (01) :134-137
[9]   Wound healing: An overview of acute, fibrotic and delayed healing [J].
Diegelmann, RF ;
Evans, MC .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2004, 9 :283-289
[10]  
Gethin G., 2007, WOUNDS UK