Tissue engineered bone-regeneration using degradable polymers: The formation of mineralized matrices

被引:105
作者
Laurencin, CT
Attawia, MA
Elgendy, HE
Herbert, KM
机构
[1] MIT,HELEN I MOOREHEAD LAURENCIN BIOMAT RES LAB,DIV HLTH SCI & TECHNOL,CAMBRIDGE,MA 02139
[2] MED COLL PENN & HAHNEMANN UNIV,DEPT ORTHOPAED SURG,PHILADELPHIA,PA
关键词
D O I
10.1016/S8756-3282(96)00132-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In the development of 3-dimensional cell-polymer matrices for tissue engineering, the ability of osteoblast cells to maintain their phenotypic properties and form. a mineralized matrix while seeded on the polymer surface is very important. Osteoblast cell differentiation and bone formation using rat calvaria cells were studied on the surface of a porous poly(lactide/glycolide)/hydroxyapatite (PLAGA/HA) 3-dimensional polymer matrix. Cell adhesion and proliferation were determined at 24 hr, 3, 7, 14, and 21 days. Cell attachment and proliferation were observed to increase throughout the first two weeks of the study, followed by a period of gradual plateauing of cell numbers. Environmental scanning electron microscopy demonstrated that cells grown on the surface of the 3-dimensional porous PLAGA/HA matrix retained their characteristic morphology and grew in a multi-layer fashion. Light microscopy observations of experiment cultures revealed active osteoblastic cells forming a characteristic mineralized matrix in the presence of 13-glycerophosphate as a phosphate donor. Mineralization did not occurred in media either not supplemented with 13-glycerophosphate or when the matrix without cells was incubated with the reagents, indicating that the mineralization was due to the cells and not the HA in the matrix. These results suggest that the 3-dimensional PLAGA/HA matrix could provide a matrix for bone cell differentiation and mineralization in vitro and, therefore, may be a candidate as a synthetic implant for bone regeneration.
引用
收藏
页码:S93 / S99
页数:7
相关论文
共 22 条
[11]   OSTEOBLAST-LIKE CELL (MC3T3-E1) PROLIFERATION ON BIOERODIBLE POLYMERS - AN APPROACH TOWARDS THE DEVELOPMENT OF A BONE BIOERODIBLE POLYMER COMPOSITE-MATERIAL [J].
ELGENDY, HM ;
NORMAN, ME ;
KEATON, AR ;
LAURENCIN, CT .
BIOMATERIALS, 1993, 14 (04) :263-269
[12]  
FRIEDLANDER G, 1991, BONE CARTILAGE ALLOG
[13]   OSTEOCALCIN AND MATRIX GLA PROTEIN - VITAMIN K-DEPENDENT PROTEINS IN BONE [J].
HAUSCHKA, PV ;
LIAN, JB ;
COLE, DEC ;
GUNDBERG, CM .
PHYSIOLOGICAL REVIEWS, 1989, 69 (03) :990-1047
[14]   OSTEOCALCIN-HYDROXYAPATITE INTERACTION IN THE EXTRACELLULAR ORGANIC MATRIX OF BONE [J].
HAUSCHKA, PV ;
WIANS, FH .
ANATOMICAL RECORD, 1989, 224 (02) :180-188
[15]  
HOLLINGER JO, 1986, CLIN ORTHOP RELAT R, V207, P290
[16]   EFFECTS OF EPIDERMAL GROWTH-FACTOR ON OSTEOBLASTIC CELLS-INVITRO [J].
KUMEGAWA, M ;
HIRAMATSU, M ;
HATAKEYAMA, K ;
YAJIMA, T ;
KODAMA, H ;
OSAKI, T ;
KURISU, K .
CALCIFIED TISSUE INTERNATIONAL, 1983, 35 (4-5) :542-548
[17]   OSTEOBLASTS ON HYDROXYAPATITE, ALUMINA AND BONE SURFACES INVITRO - MORPHOLOGY DURING THE 1ST 2-H OF ATTACHMENT [J].
MALIK, MA ;
PULEO, DA ;
BIZIOS, R ;
DOREMUS, RH .
BIOMATERIALS, 1992, 13 (02) :123-128
[18]   MINERALIZATION INVITRO OF MATRIX FORMED BY OSTEOBLASTS ISOLATED BY COLLAGENASE DIGESTION [J].
NEFUSSI, JR ;
BOYLEFEVRE, ML ;
BOULEKBACHE, H ;
FOREST, N .
DIFFERENTIATION, 1985, 29 (02) :160-168
[19]   OSTEOBLAST RESPONSES TO ORTHOPEDIC IMPLANT MATERIALS INVITRO [J].
PULEO, DA ;
HOLLERAN, LA ;
DOREMUS, RH ;
BIZIOS, R .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1991, 25 (06) :711-723
[20]  
SCHWARTZ E, 1987, CULTURE ANIMAL CELLS, P332