Histamine effects on conjunctival fibroblasts from patients with vernal conjunctivitis

被引:58
作者
Leonardi, A
Radice, M
Fregona, IA
Plebani, M
Abatangelo, G
Secchi, AG
机构
[1] Univ Padua, Dept Ophthalmol, Inst Physiopathol Opt, I-35100 Padua, Italy
[2] Univ Padua, Dept Histol & Embryol, I-35100 Padua, Italy
[3] Univ Padua, Dept Lab Med, I-35100 Padua, Italy
关键词
fibroblasts; histamine; proliferation; vernal keratoconjunctivitis;
D O I
10.1006/exer.1999.0658
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Histamine, an important mast cell mediator in allergic disorders, may affect extracellular matrix production and cell growth in vernal keratoconjunctivitis (VKC), In the present study, the histamine reactivity of conjunctival fibroblasts derived from VKC patients was investigated in vitro, Conjunctival fibroblast cultures were derived from biopses of 8 tarsal VKC patients and 5 normal subjects. These cells were maintained in vitro and stimulated with different concentrations of histamine with and without H1 (clorpheniramine) and H2 (cimetidine) receptor antagonists, Comparisons were made to fibroblasts grown in the same media without histamine and to fibroblasts stimulated with just antihistamine. The effects of histamine were evaluated by: (1) the MTT test to assess cell proliferation; (2) an in vitro wound model for cell migration and (3) the measurement of procollagen I (PIP) and procollagen III (PIIIP) in supernatants for collagen production. Results showed: (1) While VKC-derived fibroblasts proliferated at a faster rate than normal cells in unstimulated media, after histamine stimulation, VKC and normal cells grew at a similar rate. Both H1 and H2 antagonists significantly inhibited (P < 0.05) histamine-induced cell proliferation. (2) Histamine enhanced cell migration after wounding; this effect was inhibited only by H2 antagonism. (3) When stimulated with histamine, VKC fibroblasts produced significantly more PIP than those in control media. Furthermore, VKC-derived fibroblasts were more sensitive to histamine challenge, producing significantly more PIP than normal fibroblasts. H1 and H2 antagonists did not modify histamine-stimulated PIP production. The enhanced proliferative and productive capacity of VKC fibroblasts may be the result of a selective overgrowth of one or more fibroblast subpopulations in a chronically inflamed tissue. Histamine increased proliferation, migration and collagen production in both normal and VKC fibroblasts. Since H2 antagonism modulated both cell growth and migration, but not histamine-induced collagen production, the latter may be mediated by a different receptor. These results showed that histamine is at least partially responsible for fibroblast stimulation. (C) 1999 Academic Press.
引用
收藏
页码:739 / 746
页数:8
相关论文
共 30 条
[1]  
ABELSON MB, 1980, OPHTHALMOLOGY, V87, P812
[2]  
ABELSON MB, 1981, ARCH OPHTHALMOL-CHIC, V99, P302
[3]   Histaminase activity in patients with vernal keratoconjunctivitis [J].
Abelson, MB ;
Leonardi, AA ;
Smith, LM ;
Fregona, IA ;
George, MA ;
Secchi, AG .
OPHTHALMOLOGY, 1995, 102 (12) :1958-1963
[4]  
Allansmith MR, 1982, EYE IMMUNOLOGY, P118
[5]   CONJUNCTIVAL HYPERRESPONSIVENESS TO OCULAR HISTAMINE CHALLENGE IN PATIENTS WITH VERNAL CONJUNCTIVITIS [J].
BONINI, S ;
BONINI, S ;
SCHIAVONE, M ;
CENTOFANTI, M ;
ALLANSMITH, MR ;
BUCCI, MG .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1992, 89 (01) :103-107
[6]   MAST-CELLS, FIBROBLASTS, AND FIBROSIS - NEW CLUES TO THE RIDDLE OF MAST-CELLS [J].
CHOI, KL ;
CLAMAN, HN .
IMMUNOLOGIC RESEARCH, 1987, 6 (03) :145-152
[7]   RAPID COLORIMETRIC ASSAY FOR CELL-GROWTH AND SURVIVAL - MODIFICATIONS TO THE TETRAZOLIUM DYE PROCEDURE GIVING IMPROVED SENSITIVITY AND RELIABILITY [J].
DENIZOT, F ;
LANG, R .
JOURNAL OF IMMUNOLOGICAL METHODS, 1986, 89 (02) :271-277
[8]   MAST-CELLS AS A SOURCE OF MULTIFUNCTIONAL CYTOKINES [J].
GORDON, JR ;
BURD, PR ;
GALLI, SJ .
IMMUNOLOGY TODAY, 1990, 11 (12) :458-464
[9]   PROMOTION OF MOUSE FIBROBLAST COLLAGEN GENE-EXPRESSION BY MAST-CELLS STIMULATED VIA THE FC(EPSILON)RI - ROLE FOR MAST CELL-DERIVED TRANSFORMING GROWTH-FACTOR-BETA AND TUMOR-NECROSIS-FACTOR-ALPHA [J].
GORDON, JR ;
GALLI, SJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (06) :2027-2037
[10]  
HATAMOCHI A, 1991, Journal of Dermatological Science, V2, P407, DOI 10.1016/0923-1811(91)90004-H