'Young' Oral Fibroblasts Are Geno/Phenotypically Distinct

被引:24
作者
Enoch, S. [1 ]
Peake, M. A. [1 ]
Wall, I. [1 ]
Davies, L. [1 ]
Farrier, J. [1 ]
Giles, P. [2 ]
Kipling, D. [2 ]
Price, P. [3 ]
Moseley, R. [1 ]
Thomas, D. [1 ]
Stephens, P. [1 ]
机构
[1] Cardiff Univ, Cardiff Inst Tissue Engn & Repair Tissue Engn & R, Wound Biol Grp, Cardiff CF14 4XY, S Glam, Wales
[2] Cardiff Univ, Sch Med, Dept Pathol, Cardiff CF14 4XY, S Glam, Wales
[3] Cardiff Univ, Sch Med, Wound Healing Res Unit, Cardiff CF14 4XY, S Glam, Wales
关键词
wound healing; fibroblast; aging; genotype; phenotype; EXTRACELLULAR-MATRIX REORGANIZATION; SKIN FIBROBLASTS; PHENOTYPIC DIFFERENCES; DERMAL FIBROBLASTS; COLLAGEN-SYNTHESIS; WOUND CONTRACTION; GROWTH-KINETICS; VENOUS ULCERS; GELATINASE-A; METALLOPROTEINASE;
D O I
10.1177/0022034510377796
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Wound healing within the oral mucosa results in minimal scar formation compared with wounds within the skin. We have recently demonstrated distinct differences in the aging profiles of cells (oral mucosal and patient-matched skin fibroblasts) isolated from these tissues. We hypothesized that the increased replicative potential of oral mucosal fibroblasts may confer upon them preferential wound-healing capacities. Passage-matched early cultures of oral mucosal fibroblasts and skin fibroblasts demonstrated distinct gene expression profiles, with several genes linked to wound healing/tissue repair. This was related to an increased ability of the 'replicatively younger' oral mucosal fibroblasts to repopulate a wound space and reorganize their surrounding extracellular matrix environment, key activities during the wound-healing process. We conclude that oral mucosal fibroblasts exhibit a preferential healing response in vivo, due to their 'replicatively younger' phenotype when compared with that of patient-matched skin fibroblasts.
引用
收藏
页码:1407 / 1413
页数:7
相关论文
共 32 条
[1]   An investigation of preferential fibroblast wound repopulation using a novel in vitro wound model [J].
alKhateeb, T ;
Stephens, P ;
Shepherd, JP ;
Thomas, DW .
JOURNAL OF PERIODONTOLOGY, 1997, 68 (11) :1063-1069
[2]  
[Anonymous], 2006, R LANG ENV STAT COMP
[3]   HYALURONAN AND WOUND-HEALING - A NEW PERSPECTIVE [J].
BURD, DAR ;
GRECO, RM ;
REGAUER, S ;
LONGAKER, MT ;
SIEBERT, JW ;
GARG, HG .
BRITISH JOURNAL OF PLASTIC SURGERY, 1991, 44 (08) :579-584
[4]   Gene expression signature of fibroblast serum response predicts human cancer progression: Similarities between tumors and wounds [J].
Chang, HY ;
Sneddon, JB ;
Alizadeh, AA ;
Sood, R ;
West, RB ;
Montgomery, K ;
Chi, JT ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PLOS BIOLOGY, 2004, 2 (02) :206-214
[5]   Diversity, topographic differentiation, and positional memory in human fibroblasts [J].
Chang, HY ;
Chi, JT ;
Dudoit, S ;
Bondre, C ;
van de Rijn, M ;
Botstein, D ;
Brown, PO .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12877-12882
[6]   Defective extracellular matrix reorganization by chronic wound fibroblasts is associated with alterations in TIMP-1, TIMP-2, and MMP-2 activity [J].
Cook, H ;
Stephens, P ;
Davies, KJ ;
Harding, KG ;
Thomas, DW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2000, 115 (02) :225-233
[7]   DAVID: Database for annotation, visualization, and integrated discovery [J].
Dennis, G ;
Sherman, BT ;
Hosack, DA ;
Yang, J ;
Gao, W ;
Lane, HC ;
Lempicki, RA .
GENOME BIOLOGY, 2003, 4 (09)
[8]   GROWTH KINETICS AND COLLAGEN-SYNTHESIS OF NORMAL SKIN, NORMAL SCAR AND KELOID FIBROBLASTS INVITRO [J].
DIEGELMANN, RF ;
COHEN, IK ;
MCCOY, BJ .
JOURNAL OF CELLULAR PHYSIOLOGY, 1979, 98 (02) :341-346
[9]  
Duncan BW., 1992, FETAL WOUND HEALING, P303
[10]   Increased Oral Fibroblast Lifespan Is Telomerase-independent [J].
Enoch, S. ;
Wall, I. ;
Peake, M. ;
Davies, L. ;
Farrier, J. ;
Giles, P. ;
Baird, D. ;
Kipling, D. ;
Price, P. ;
Moseley, R. ;
Thomas, D. ;
Stephens, P. .
JOURNAL OF DENTAL RESEARCH, 2009, 88 (10) :916-921