A Novel Mouse Model of Cutaneous Radiation Injury

被引:58
作者
Thanik, Vishal D. [1 ]
Chang, Christopher C. [1 ]
Zoumalan, Richard A. [1 ]
Lerman, Oren Z. [1 ]
Allen, Robert J., Jr. [1 ]
Nguyen, Phuong D. [1 ]
Warren, Stephen M. [1 ]
Coleman, Sydney R. [1 ]
Hazen, Alexes [1 ]
机构
[1] NYU, Sch Med, Inst Reconstruct Plast Surg Labs, New York, NY 10016 USA
关键词
IMPAIRED WOUNDS; IRRADIATED SKIN; FIBROSIS; ALOPECIA; RADIOBIOLOGY; RESPONSES; CELLS; SMAD3;
D O I
10.1097/PRS.0b013e3181fed4f7
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Radiation therapy is a cornerstone of oncologic treatment. Skin tolerance is often the limiting factor in radiotherapy. To study these issues and create modalities for intervention, the authors developed a novel murine model of cutaneous radiation injury. Methods: The dorsal skin was isolated using a low-pressure clamp and irradiated. Mice were followed for 8 weeks with serial photography and laser Doppler analysis. Sequential skin biopsy specimens were taken and examined histologically. Tensiometry was performed and Young's modulus calculated. Results: High-dose radiation isolated to dorsal skin causes progressive changes in skin perfusion, resulting in dermal thickening, fibrosis, persistent alopecia, and sometimes ulceration. There is increased dermal Smad3 expression, and decreased elasticity and bursting strength. Conclusions: This model of cutaneous radiation injury delivers reproducible localized effects, mimicking the injury pattern seen in human subjects. This technique can be used to study radiation-induced injury to evaluate preventative and therapeutic strategies for these clinical issues. (Plast. Reconstr. Surg. 127: 560, 2011.)
引用
收藏
页码:560 / 568
页数:9
相关论文
共 27 条
[1]   PATHOPHYSIOLOGY OF IRRADIATED SKIN AND BREAST [J].
ARCHAMBEAU, JO ;
PEZNER, R ;
WASSERMAN, T .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1995, 31 (05) :1171-1185
[2]   A systems biology approach to multicellular and multi-generational radiation responses [J].
Barcellos-Hoff, Mary Helen ;
Costes, Sylvain V. .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2006, 597 (1-2) :32-38
[3]   COLLAGEN GENE-EXPRESSION AND WOUND STRENGTH IN NORMAL AND RADIATION-IMPAIRED WOUNDS - A MODEL OF RADIATION-IMPAIRED WOUND-HEALING [J].
BERNSTEIN, EF ;
SALOMON, GD ;
HARISIADIS, L ;
TALBOT, T ;
HARRINGTON, F ;
RUSSO, A ;
UITTO, J .
JOURNAL OF DERMATOLOGIC SURGERY AND ONCOLOGY, 1993, 19 (06) :564-570
[4]   TRANSFORMING GROWTH-FACTOR-BETA IMPROVES HEALING OF RADIATION-IMPAIRED WOUNDS [J].
BERNSTEIN, EF ;
HARISIADIS, L ;
SALOMON, G ;
NORTON, J ;
SOLLBERG, S ;
UITTO, J ;
GLATSTEIN, E ;
GLASS, J ;
TALBOT, T ;
RUSSO, A ;
MITCHELL, JB .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1991, 97 (03) :430-434
[5]  
Cuscela D, 1996, Cancer J Sci Am, V2, P273
[6]   Smad-dependent and Smad-independent pathways in TGF-β family signalling [J].
Derynck, R ;
Zhang, YE .
NATURE, 2003, 425 (6958) :577-584
[7]   Smads:: Transcriptional activators of TGF-β responses [J].
Derynck, R ;
Zhang, Y ;
Feng, XH .
CELL, 1998, 95 (06) :737-740
[8]   A review of human cell radiosensitivity in vitro [J].
Deschavanne, PJ ;
Fertil, B .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1996, 34 (01) :251-266
[9]   FACTORS INFLUENCING MYOFIBROBLAST DIFFERENTIATION DURING WOUND-HEALING AND FIBROSIS [J].
DESMOULIERE, A .
CELL BIOLOGY INTERNATIONAL, 1995, 19 (05) :471-476
[10]   Interference with transforming growth factor-β/Smad3 signaling results in accelerated healing of wounds in previously irradiated skin [J].
Flanders, KC ;
Major, CD ;
Arabshahi, A ;
Aburime, EE ;
Okada, MH ;
Fujii, M ;
Blalock, TD ;
Schultz, GS ;
Sowers, A ;
Anzano, MA ;
Mitchell, JB ;
Russo, A ;
Roberts, AB .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (06) :2247-2257