Evolving concepts in bone tissue engineering

被引:55
作者
Cowan, CM [1 ]
Soo, C
Ting, K
Wu, B
机构
[1] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Weintraub Ctr Reconstruct Biotechnol, Los Angeles, CA 90095 USA
[3] Univ So Calif, Keck Sch Med, Div Plast Surg, Los Angeles, CA 90053 USA
来源
CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY, VOL 66 | 2005年 / 66卷
关键词
D O I
10.1016/S0070-2153(05)66008-5
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
The field of tissue engineering integrates the latest advances in molecular biology, biochemistry, engineering, material science, and medical transplantation. Researchers in the developing field of regenerative medicine have identified bone tissue engineering as an attractive translational target. Clinical problems requiring bone regeneration are diverse, and no single regeneration approach will likely resolve all defects. Recent advances in the field of tissue engineering have included the use of sophisticated biocompatible scaffolds, new postnatal multipotent cell populations, and the appropriate cellular stimulation. In particular, synthetic polymer scaffolds allow for fast and reproducible construction, while still retaining biocompatible characteristics. These criteria relate to the immediate goal of determining the ideal implant. The search is becoming a reality with widespread availability of biocompatible scaffolds; however, the desired parameters have not been clearly defined. Currently, most research focuses on the use of bone morphogenetic proteins (BMPs), specifically BMP-2 and BMP-7. These proteins induce osteogenic differentiation in vitro, as well as bone defect healing in vivo. Protein-scaffold interactions that enhance BMP binding are of the utmost importance, since prolonged BMP release creates the most osteogenic microenvironment. Transition into clinical studies has had only mild success and relies on large doses of BMPs for bone formation. Advances within the field of bone tissue engineering will likely overcome these challenges and lead to more clinically relevant therapies. (c) 2005, Elsevier Inc.
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页码:239 / +
页数:48
相关论文
共 263 条
[1]
Applications of a mouse model of calvarial healing: Differences in regenerative abilities of juveniles and adults [J].
Aalami, OO ;
Nacamuli, RP ;
Lenton, KA ;
Cowan, CM ;
Fang, TD ;
Fong, KD ;
Shi, YY ;
Song, HM ;
Sahar, DE ;
Longaker, MT .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2004, 114 (03) :713-720
[2]
The role of ultrasound in monitoring reconstruction of mandibular continuity defects using osteogenic protein-1 (rhOP-1) [J].
Abu-Serriah, M ;
Ayoub, A ;
Boyd, J ;
Paterson, C ;
Wray, D .
INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY, 2003, 32 (06) :619-627
[3]
Antibiotic microspheres: Preliminary testing for potential treatment of osteomyelitis [J].
Ambrose, CG ;
Gogola, GR ;
Clyburn, TA ;
Raymond, AK ;
Peng, AS ;
Mikos, AG .
CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2003, (415) :279-285
[4]
Bone morphogenetic protein (BMP) localization in developing human and rat growth plate, metaphysis, epiphysis, and articular cartilage [J].
Anderson, HC ;
Hodges, PT ;
Aguilera, XM ;
Missana, L ;
Moylan, PE .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (11) :1493-1502
[5]
[Anonymous], 2002, NEUROSURG FOCUS, DOI DOI 10.3171/FOC.2002.13.6.3
[6]
POTENT ECTOPIC BONE-INDUCING ACTIVITY OF BONE MORPHOGENETIC PROTEIN-4/7 HETERODIMER [J].
AONO, A ;
HAZAMA, M ;
NOTOYA, K ;
TAKETOMI, S ;
YAMASAKI, H ;
TSUKUDA, R ;
SASAKI, S ;
FUJISAWA, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 210 (03) :670-677
[7]
HUMAN OSTEOGENIC PROTEIN-1 INDUCES BOTH CHONDROBLASTIC AND OSTEOBLASTIC DIFFERENTIATION OF OSTEOPROGENITOR CELLS DERIVED FROM NEWBORN RAT CALVARIA [J].
ASAHINA, I ;
SAMPATH, TK ;
NISHIMURA, I ;
HAUSCHKA, PV .
JOURNAL OF CELL BIOLOGY, 1993, 123 (04) :921-933
[8]
In vitro differentiation of human processed lipoaspirate cells into early neural progenitors [J].
Ashjian, PH ;
Elbarbary, AS ;
Edmonds, B ;
DeUgarte, D ;
Zhu, M ;
Zuk, PA ;
Lorenz, HP ;
Benhaim, P ;
Hedrick, MH .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2003, 111 (06) :1922-1931
[9]
Regional gene therapy to enhance bone repair [J].
Baltzer, AWA ;
Lieberman, JR .
GENE THERAPY, 2004, 11 (04) :344-350
[10]
Fluid flow increases mineralized matrix deposition in 3D perfusion culture of marrow stromal osteloblasts in a dose-dependent manner [J].
Bancroft, GN ;
Sikavitsast, VI ;
van den Dolder, J ;
Sheffield, TL ;
Ambrose, CG ;
Jansen, JA ;
Mikos, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (20) :12600-12605