Myofibroblasts. II. Intestinal subepithelial myofibroblasts

被引:439
作者
Powell, DW
Mifflin, RC
Valentich, JD
Crowe, SE
Saada, JI
West, AB
机构
[1] Univ Texas, Med Branch, Dept Internal Med, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Physiol, Galveston, TX 77555 USA
[3] Univ Texas, Med Branch, Dept Biophys & Pathol, Galveston, TX 77555 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 02期
关键词
interstitial cells of Cajal; cyclooxygenase; chemoprevention; wound repair; fibrosis; electrolyte transport; immunophysiology;
D O I
10.1152/ajpcell.1999.277.2.C183
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Intestinal subepithelial myofibroblasts (ISEMF) and the interstitial cells of Cajal are the two types of myofibroblasts identified in the intestine. Intestinal myofibroblasts are activated and proliferate in response to various growth factors, particularly the platelet-derived growth factor (PDGF) family, which includes PDGF-BB and stem cell factor (SCF), through expression of PDGF receptors and the SCF receptor c-hit. ISEMF have been shown to play important roles in the organogenesis of the intestine, and growth factors and cytokines secreted by these cells promote epithelial restitution and proliferation, i.e,, wound repair. Their role in the fibrosis of Crohn's disease and collagenous colitis is being investigated. Through cyclooxygenase (COX)-1 and COX-2 activation, ISEMF augment intestinal ion secretion in response to certain secretagogues. By forming a subepithelial barrier to Na+ diffusion, they create a hypertonic compartment that may account for the ability of the gut to transport fluid against an adverse osmotic gradient. Through the paracrine secretion of prostaglandins and growth factors (e.g., transforming growth factor-beta), ISEMF may play a role in colonic tumorigenesis and metastasis. COX-2 in polyp ISEMF may be a target for nonsteroidal anti-inflammatory drugs (NSAIDs), which would account for the regression of the neoplasms in familial adenomatous polyposis and the preventive effect of NSAIDs in the development of sporadic colon neoplasms. More investigation is needed to clarify the functions of these pleiotropic cells.
引用
收藏
页码:C183 / C201
页数:19
相关论文
共 234 条
[1]   Extracellular matrix composition and gene expression in collagenous colitis [J].
Aigner, T ;
Neureiter, D ;
Muller, S ;
Kuspert, G ;
Belke, J ;
Kirchner, T .
GASTROENTEROLOGY, 1997, 113 (01) :136-143
[2]   Transforming growth factor beta type II receptor gene mutations in adenomas from hereditary nonpolyposis colorectal cancer [J].
Akiyama, Y ;
Iwanaga, R ;
Saitoh, K ;
Shiba, K ;
Ushio, K ;
Ikeda, E ;
Iwama, T ;
Nomizu, T ;
Yuasa, Y .
GASTROENTEROLOGY, 1997, 112 (01) :33-39
[3]   A MORPHOLOGICAL-STUDY ON THE HISTOGENESIS OF HUMAN COLORECTAL HYPERPLASTIC POLYPS [J].
ARAKI, K ;
OGATA, T ;
KOBAYASHI, M ;
YATANI, R .
GASTROENTEROLOGY, 1995, 109 (05) :1468-1474
[4]   Expression of transforming growth factors alpha and beta in colonic mucosa in inflammatory bowel disease [J].
Babyatsky, MW ;
Rossiter, G ;
Podolsky, DK .
GASTROENTEROLOGY, 1996, 110 (04) :975-984
[5]   Interactions between stromal cell-derived keratinocyte growth factor and epithelial transforming growth factor in immune-mediated crypt cell hyperplasia [J].
Bajaj-Elliott, M ;
Poulsom, R ;
Pender, SLF ;
Wathen, NC ;
MacDonald, TT .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (08) :1473-1480
[6]   Chemoprevention of spontaneous intestinal adenomas in the adenomatous polyposis coli Min mouse model with aspirin [J].
Barnes, CJ ;
Lee, M .
GASTROENTEROLOGY, 1998, 114 (05) :873-877
[7]  
BARRETT KE, 1993, AM J PHYSIOL, V265, pC859
[8]   Expression pattern of heme oxygenase isoenzymes 1 and 2 in normal and stress-exposed rat liver [J].
Bauer, I ;
Wanner, GA ;
Rensing, H ;
Alte, G ;
Miescher, EA ;
Wolf, B ;
Pannen, BHJ ;
Clemens, MG ;
Bauer, M .
HEPATOLOGY, 1998, 27 (03) :829-838
[9]   Adult human colonic subepithelial myofibroblasts (HCSM) regulate epithelial secretory response and barrier function via distinct pathways. [J].
Beltinger, J ;
Makh, S ;
Stack, WA ;
Hawkey, CJ ;
Mahida, YR .
GASTROENTEROLOGY, 1998, 114 (04) :A1128-A1128
[10]  
Bernex F, 1996, DEVELOPMENT, V122, P3023