Mesothelial progenitor cells and their potential in tissue engineering

被引:106
作者
Herrick, SE
Mutsaers, SE
机构
[1] Univ Manchester, Sch Biol Sci, Manchester M13 9PT, Lancs, England
[2] Univ Western Australia, Dept Med, Asthma & Allergy Res Inst, Nedlands, WA 6009, Australia
基金
英国医学研究理事会;
关键词
peritoneum; stem cells; epithelial-mesenchymal transitions; adhesions; serosa;
D O I
10.1016/j.biocel.2003.11.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mesothelium consists of a single layer of flattened mesothelial cells that lines serosal cavities and the majority of internal organs, playing important roles in maintaining normal serosal integrity and function. A mesothelial 'stem' cell has not been identified, but evidence from numerous studies suggests that a progenitor mesothelial cell exists. Although mesothelial cells are of a mesodermal origin, they express characteristics of both epithelial and mesenchymal phenotypes. In addition, following injury, new mesothelium regenerates via centripetal ingrowth of cells from the wound edge and from a free-floating population of cells present in the serosal fluid, the origin of which is currently unknown. Recent findings have shown that mesothelial cells can undergo an epithelial to mesenchymal transition, and transform into myofibroblasts and possibly smooth muscle cells, suggesting plasticity in nature. Further evidence for a mesothelial progenitor comes from tissue engineering applications where mesothelial cells seeded onto tubular constructs have been used to generate vascular replacements and grafts to bridge transected nerve fibres. These findings suggest that mesothelial cell progenitors are able to switch between different cell phenotypes depending on the local environment. However, only by performing detailed investigations involving selective cell isolation, clonal analysis together with cell labelling and tracking studies, will we begin to determine the true existence of a mesothelial stem cell. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:621 / 642
页数:22
相关论文
共 177 条
[1]   Proliferation of rat pleural mesothelial cells in response to hepatocyte and keratinocyte growth factors [J].
Adamson, IYR ;
Bakowska, J ;
Prieditis, H .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2000, 23 (03) :345-349
[2]   Diagnostic use of muscle markers in the cytologic evaluation of serous fluids [J].
Afify, AM ;
Al-Khafaji, BM ;
Paulino, AFG ;
Davila, RM .
APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2002, 10 (02) :178-182
[3]   STRUCTURE, BLOOD-SUPPLY, AND LYMPHATIC VESSELS OF THE SHEEPS VISCERAL PLEURA [J].
ALBERTINE, KH ;
WIENERKRONISH, JP ;
ROOS, PJ ;
STAUB, NC .
AMERICAN JOURNAL OF ANATOMY, 1982, 165 (03) :277-294
[4]   Immunohistochemical and ultrastructural study on effect of fibroblast growth factor on transformation of fibroblasts to regenerated mesothelial cells [J].
Amari M. ;
Taguchi K. ;
Iwahara M. ;
Shibuya K. ;
Naoe S. .
Medical Electron Microscopy, 2002, 35 (4) :225-233
[5]   SARCOMATOUS TUMOR OF THE CHEST WALL WITH OSTEOCHONDROID DIFFERENTIATION - EVIDENCE OF MESOTHELIAL ORIGIN [J].
ANDRION, A ;
MAZZUCCO, G ;
BERNARDI, P ;
MOLLO, F .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1989, 13 (08) :707-712
[6]   SCANNING ELECTRON-MICROSCOPE STUDY OF MOUSE PERITONEAL MESOTHELIUM [J].
BARADI, AF ;
RAO, SN .
TISSUE & CELL, 1976, 8 (01) :159-162
[7]  
BARADI AF, 1974, ARCH PATHOL, V97, P2
[8]  
BEARN PE, 1992, INT J EXP PATHOL, V73, P801
[9]   Adhesion molecule-dependent mechanisms regulate the rate of macrophage clearance during the resolution of peritoneal inflammation [J].
Bellingan, GJ ;
Xu, P ;
Cooksley, H ;
Cauldwell, H ;
Shock, A ;
Bottoms, S ;
Haslett, C ;
Mutsaers, SE ;
Laurent, GJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2002, 196 (11) :1515-1521
[10]  
Bertram P, 1999, EUR J SURG, V165, P705