Remodeling of peritoneal-like structures by mesothelial cells:: Its role in peritoneal healing

被引:32
作者
Bittinger, F
Schepp, C
Brochhausen, C
Lehr, HA
Otto, M
Köhler, H
Skarke, C
Walgenbach, S
Kirkpatrick, CJ
机构
[1] Univ Mainz, Inst Pathol, Dept Pathol, D-55101 Mainz, Germany
[2] Univ Mainz, Dept Surg, D-55101 Mainz, Germany
关键词
mesothelial cells; adhesion formation; mesothelial healing; altered phenotype;
D O I
10.1006/jsre.1998.5449
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Intraabdominal adhesions are a common complication following laparotomy. Since the exact mechanisms involved in this processes are unknown we have analyzed in vitro the role of mesothelial cells in peritoneal healing. Material and methods. Human mesothelial cells from omental tissue were cultivated for 2 weeks in a three-dimensional culture either on or in a collagen type I matrix. The effects of blood and collagen matrix were analyzed by exposing mesothelial cells to an overlying blood clot, simulating intraperitoneal bleeding, or a second collagen layer. The production of collagen types III and IV, fibronectin, and laminin was analyzed with immunohistochemical methods. Results. Mesothelial cells grown on a collagen matrix formed a monolayer of flat or cobblestone-like cells whereas those cultivated in a collagen matrix exhibited spindle-like morphology. Mesothelial cells failed to grow into an overlying collagen matrix, but did grow into a blood clot, emphasizing a potential role of blood clots in peritoneal adhesion formation. Independent of the culture systems mesothelial cells produced collagen type III, fibronectin, and laminin but not collagen type IV. Conclusions. Our experiments demonstrate remodeling of peritoneal-like structures by mesothelial cells in a three-dimensional culture reflecting their putative role in the reepithelialization after serosal defects, and also in the formation of peritoneal adhesions. (C) 1999 Academic Press.
引用
收藏
页码:28 / 33
页数:6
相关论文
共 31 条
[1]   Reconstruction of peritoneal-like structure in three-dimensional collagen gel matrix culture [J].
Bittinger, F ;
Brochhausen, C ;
Skarke, C ;
Kohler, H ;
Kirkpatrick, CJ .
EXPERIMENTAL CELL RESEARCH, 1997, 236 (01) :155-160
[2]   REACTIVE AND NEOPLASTIC SEROSAL TISSUE - A LIGHT-MICROSCOPIC, ULTRASTRUCTURAL, AND IMMUNOCYTOCHEMICAL STUDY [J].
BOLEN, JW ;
HAMMAR, SP ;
MCNUTT, MA .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1986, 10 (01) :34-47
[3]  
BREBOROWICZ A, 1991, PERITON DIALYSIS INT, V11, P228
[4]   REGULATION OF THE CYTOSKELETON IN MESOTHELIAL CELLS - REVERSIBLE LOSS OF KERATIN AND INCREASE IN VIMENTIN DURING RAPID GROWTH IN CULTURE [J].
CONNELL, ND ;
RHEINWALD, JG .
CELL, 1983, 34 (01) :245-253
[5]  
DAVILA RM, 1993, AM J PATHOL, V142, P547
[6]   MORPHOLOGY OF THE PERITONEUM IN CAPD [J].
DOBBIE, JW .
BLOOD PURIFICATION, 1989, 7 (2-3) :74-85
[7]  
ELLIS H, 1971, SURG GYNECOL OBSTETR, V133, P497
[8]  
HJELLE JT, 1995, PERITON DIALYSIS INT, V15, P13
[9]   MESOTHELIAL CELL RESPONSE TO PLEURAL INJURY - THROMBIN-INDUCED PROLIFERATION AND CHEMOTAXIS OF RAT PLEURAL MESOTHELIAL CELLS [J].
HOTT, JW ;
SPARKS, JA ;
GODBEY, SW ;
ANTONY, VB .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1992, 6 (04) :421-425
[10]  
JONECKO A, 1990, Z MIKROSK ANAT FORSC, V104, P907