Tissue engineering for cutaneous wounds

被引:381
作者
Clark, Richard A. F.
Ghosh, Kaustabh
Tonnesen, Marcia G.
机构
[1] SUNY Stony Brook, Hlth Sci Ctr, Dept Biomed Engn, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Dermatol, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Med, Stony Brook, NY 11794 USA
[4] Northport VAMC, Med Serv, Dept Dermatol, Northport, NY USA
关键词
D O I
10.1038/sj.jid.5700715
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Skin, the largest organ in the body, protects against toxins and microorganisms in the environment and serves to prevent dehydration of all non-aquatic animals. Immune surveillance, sensory detection, and self-healing are other critical functions of the skin. Loss of skin integrity because of injury or illness may result acutely in substantial physiologic imbalance and ultimately in significant disability or even death. It is estimated that, in 1992, there were 35.2 million cases of significant skin loss (US data) that required major therapeutic intervention. Of these, approximately 7 million wounds become chronic. Regardless of the specific advanced wound care product, the ideal goal would be to regenerate tissues such that both the structural and functional properties of the wounded tissue are restored to the levels before injury. The advent of tissue-engineered skin replacements revolutionized the therapeutic potential for recalcitrant wounds and for wounds that are not amenable to primary closure. This article will introduce the reader to the field of tissue engineering, briefly review tissue-engineered skin replacement from a historical perspective and then review current state-of-the-art concepts from our vantage point.
引用
收藏
页码:1018 / 1029
页数:12
相关论文
共 114 条
[1]   Xenografts are an achievable breakthrough [J].
Alisky, JM .
MEDICAL HYPOTHESES, 2004, 63 (01) :92-97
[2]  
*AM BURN ASS, 2005, BURN INC TREATM US 2
[3]   Estrogen modulates cutaneous wound healing by downregulating macrophage migration inhibitory factor [J].
Ashcroft, GS ;
Mills, SJ ;
Lei, KJ ;
Gibbons, L ;
Jeong, MJ ;
Taniguchi, M ;
Burow, M ;
Horan, MA ;
Wahl, SM ;
Nakayama, T .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (09) :1309-1318
[4]   Participation of bone marrow derived cells in cutaneous wound healing [J].
Badiavas, EV ;
Abedi, M ;
Butmarc, J ;
Falanga, V ;
Quesenberry, P .
JOURNAL OF CELLULAR PHYSIOLOGY, 2003, 196 (02) :245-250
[5]   Skin substitutes: a review [J].
Balasubramani, M ;
Kumar, TR ;
Babu, M .
BURNS, 2001, 27 (05) :534-544
[6]   Crosstalk between extrinsic and intrinsic cell death pathways in pancreatic cancer: Synergistic action of estrogen metabolite and ligands of death receptor family [J].
Basu, A ;
Castle, VP ;
Bouziane, M ;
Bhalla, K ;
Haldar, S .
CANCER RESEARCH, 2006, 66 (08) :4309-4318
[7]   LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[8]   PRODUCTION OF A TISSUE-LIKE STRUCTURE BY CONTRACTION OF COLLAGEN LATTICES BY HUMAN-FIBROBLASTS OF DIFFERENT PROLIFERATIVE POTENTIAL INVITRO [J].
BELL, E ;
IVARSSON, B ;
MERRILL, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (03) :1274-1278
[9]   Tissue engineering firms go under [J].
Bouchie, A .
NATURE BIOTECHNOLOGY, 2002, 20 (12) :1178-1179
[10]   Hyaluronan-CD44 interaction stimulates keratinocyte differentiation, lamellar body formation/secretion, and permeability barrier homeostasis [J].
Bourguignon, Lilly Y. W. ;
Ramez, Mohamed ;
Gilad, Eli ;
Singleton, Patrick A. ;
Man, Mao-Qiang ;
Crumrine, Debra A. ;
Elias, Peter M. ;
Feingold, Kenneth R. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (06) :1356-1365