Differential cutaneous wound healing in thermally injured MRL/MPJ mice

被引:24
作者
Davis, Thomas A.
Amare, Mihret
Naik, Shruti
Kovalchuk, Alexander L.
Tadaki, Douglas
机构
[1] USN, Med Res Ctr, Regenerat Med Dept, Silver Spring, MD 20910 USA
[2] Henry M Jackson Fdn, Rockville, MD USA
关键词
D O I
10.1111/j.1524-475X.2007.00266.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Adult wound repair occurs with an initial inflammatory response, reepithelialization, and the formation of a permanent scar. MRL/MpJ mice following ear-hole punch biopsies display accelerated healing and tissue regeneration. In this study, we characterized the healing responses in both MRL/MpJ and BALB/c mice following a 15% total body surface area full-thickness cutaneous burn injury. Macroscopic and histological observations show that delayed wound closure in MRL/MpJ mice is accompanied by an increase in edema, reduced neutrophil infiltration, and more prominent eschar. In vivo bromodeoxyuridine labeling showed no defect in keratinocyte proliferation and migration (reepithelialization). In comparison with BALB/c mice, MRL/MpJ wounds had greater collagen deposition, less granulation tissue formation, and contained fewer a-smooth muscle actin-positive myofibroblasts. An observed reduction in dermal neutrophil infiltration and myofibroblast development correlated with enhanced angiogenesis. Overall, BALB/c wounds contracted sooner and to a larger degree, resulting in a significant decrease in scar formation. Interestingly, MRL/MpJ mice showed overt abnormalities in hair follicle proliferation, morphogenesis, and subsequent hair regrowth postburn injury. No substantial evidence of tissue regeneration was observed in either BALB/c or MRL/MpJ wounds. Our results convincingly demonstrate that MRL/MpJ skin burn wounds heal with scar formation with delays in two critical wound healing events: wound closure, and myofibroblast development.
引用
收藏
页码:577 / 588
页数:12
相关论文
共 40 条
[1]
Alleva DG, 1997, J IMMUNOL, V159, P5610
[2]
Smad3 deficiency alters key structural elements of the extracellular matrix and mechanotransduction of wound closure [J].
Arany, PR ;
Flanders, KC ;
Kobayashi, T ;
Kuo, CK ;
Stuelten, C ;
Desai, KV ;
Tuan, R ;
Rennard, SI ;
Roberts, AB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (24) :9250-9255
[3]
Mice lacking Smad3 show accelerated wound healing and an impaired local inflammatory response [J].
Ashcroft, GS ;
Yang, X ;
Glick, AB ;
Weinstein, M ;
Letterio, JJ ;
Mizel, DE ;
Anzano, M ;
Greenwell-Wild, T ;
Wahl, SM ;
Deng, CX ;
Roberts, AB .
NATURE CELL BIOLOGY, 1999, 1 (05) :260-266
[4]
Location of injury influences the mechanisms of both regeneration and repair within the MRL/MpJ mouse [J].
Beare, Alice H. M. ;
Metcalfe, Anthony D. ;
Ferguson, Mark W. J. .
JOURNAL OF ANATOMY, 2006, 209 (04) :547-559
[5]
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[6]
A new murine model for mammalian wound repair and regeneration [J].
Clark, LD ;
Clark, RK ;
Heber-Katz, E .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1998, 88 (01) :35-45
[7]
Skin wounds in the MRL/MPJ mouse heal with scar [J].
Colwell, AS ;
Krummel, TM ;
Kong, W ;
Longaker, MT ;
Lorenz, HP .
WOUND REPAIR AND REGENERATION, 2006, 14 (01) :81-90
[8]
Prior injury accelerates subsequent wound closure in a mouse model of regeneration [J].
Davis, TA ;
Longcor, JD ;
Hicok, KC ;
Lennon, GG .
CELL AND TISSUE RESEARCH, 2005, 320 (03) :417-426
[9]
Accelerated wound closure in neutrophil-depleted mice [J].
Dovi, JV ;
He, LK ;
DiPietro, LA .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (04) :448-455
[10]
PHENOTYPIC AND FUNCTIONAL FEATURES OF MYOFIBROBLASTS IN SHEEP FETAL WOUNDS [J].
ESTES, JM ;
VANDEBERG, JS ;
ADZICK, NS ;
MACGILLIVRAY, TE ;
DESMOULIERE, A ;
GABBIANI, G .
DIFFERENTIATION, 1994, 56 (03) :173-181