Time course of membrane microarchitecture-driven neovascularization

被引:67
作者
Padera, RF
Colton, CK
机构
[1] HARVARD UNIV,MIT,DEPT CHEM ENGN,CAMBRIDGE,MA 02139
[2] HARVARD UNIV,MIT,DIV HLTH SCI & TECHNOL,CAMBRIDGE,MA 02139
关键词
in vivo; neovascularization; biocompatibility; inflammatory response;
D O I
10.1016/0142-9612(96)85565-7
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The host response to a microporous material that induces neovascularization at the material-tissue interface was studied in terms of the number and types of cells invading the membrane, the degree of vascularization at the material-tissue interface, and the characteristics of the surrounding connective tissue as a function of time following implantation. Millipore-MF mixed esters of cellulose membranes with a nominal pore diameter of 8.0 mu m were implanted subcutaneously into male Sprague-Dawley rats and explanted at 3, 5, 7, 10, 21 and 329 days post-implantation. Two samples from each of two devices at each implantation time were embedded in paraffin, sectioned to a thickness of 5 mu m, and stained with haematoxylin and eosin for light microscopic observation. The density of cells in the membrane increased up to 7 days following implantation, then remained roughly constant through 21 days and decreased at the 329 day time point. The vascularity of the material-tissue interface increased up to 10 days and remained at this level even at 329 days post-implantation. The connective tissue was disorganized, loose and avascular at 3 days, resembled granulation tissue at 5 days, and underwent fibrous capsule formation and maturation starting at 7 days following implantation.
引用
收藏
页码:277 / 284
页数:8
相关论文
共 24 条
[1]   VASCULAR-PERMEABILITY FACTOR (VASCULAR ENDOTHELIAL GROWTH-FACTOR) GENE IS EXPRESSED DIFFERENTIALLY IN NORMAL-TISSUES, MACROPHAGES, AND TUMORS [J].
BERSE, B ;
BROWN, LF ;
VANDEWATER, L ;
DVORAK, HF ;
SENGER, DR .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :211-220
[2]  
BRAUKER J, 1992, 4 WORLD BIOM C BERL, P685
[3]  
BRAUKER J, 1992, 4 WORLD BIOM C BERL, P676
[4]   NEOVASCULARIZATION OF SYNTHETIC MEMBRANES DIRECTED BY MEMBRANE MICROARCHITECTURE [J].
BRAUKER, JH ;
CARRBRENDEL, VE ;
MARTINSON, LA ;
CRUDELE, J ;
JOHNSTON, WD ;
JOHNSON, RC .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1995, 29 (12) :1517-1524
[5]   FOREIGN-BODY REACTION - CHRONIC INFLAMMATORY RESPONSE [J].
COLEMAN, DL ;
KING, RN ;
ANDRADE, JD .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH, 1974, 8 (05) :199-211
[6]   BIOENGINEERING IN DEVELOPMENT OF THE HYBRID ARTIFICIAL PANCREAS [J].
COLTON, CK ;
AVGOUSTINIATOS, ES .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1991, 113 (02) :152-170
[7]   IMPLANTABLE BIOHYBRID ARTIFICIAL ORGANS [J].
COLTON, CK .
CELL TRANSPLANTATION, 1995, 4 (04) :415-436
[8]  
COLTON CK, 1992, ANN M AM I CHEM ENG
[9]  
FREEMAN CL, 1989, MATER RES SOC S P, V110, P773
[10]   HYPOXIA INCREASES PRODUCTION OF INTERLEUKIN-1 AND TUMOR-NECROSIS-FACTOR BY HUMAN MONONUCLEAR-CELLS [J].
GHEZZI, P ;
DINARELLO, CA ;
BIANCHI, M ;
ROSANDICH, ME ;
REPINE, JE ;
WHITE, CW .
CYTOKINE, 1991, 3 (03) :189-194