Luteal leukocytes are modulators of the steroidogenic process of human mid-luteal cells

被引:30
作者
Castro, A
Castro, O
Troncoso, JL
Kohen, P
Simón, C
Vega, M
Devoto, L [1 ]
机构
[1] Univ Chile, Natl Hlth Serv, Hosp San Borja Arriaran, Sch Med,Inst Invest Materno Infantil, Santiago, Chile
[2] Univ Valencia, Dept Obstet & Gynaecol, E-46003 Valencia, Spain
关键词
corpus luteum; flow cytometry; interleukin-1; beta; leukocyte; steroidogenesis;
D O I
10.1093/humrep/13.6.1584
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Flow cytometry analysis of luteal cells revealed that an important proportion of these cells are leukocytes. The percentage of leukocytes was higher in the early (42 +/- 4) and late (35 +/- 3) luteal phases than in the mid-luteal (24 +/- 2) phase. However, the proportion of macrophages did not differ between the luteal stages. The how cytometric properties correlated with cellular size and granularity were not reliable as discriminators of luteal cell subpopulations. Therefore, to assess the contribution of luteal leukocytes, these cells mere completely removed from luteal cell suspensions (total cells), by a negative selection procedure (immunomagnetic separation), The functional role of leukocytes in mid-luteal steroidogenesis was assessed, in total as well as leukocyte-depleted cells. Progesterone production was found to have increased 2.2-fold in leukocyte-depleted cell cultures, in comparison with total cells under basal conditions. However, the response to human chorionic gonadotrophin (HCG) was 36% lower under the latter conditions. Oestradiol production was not significantly modified under basal or HCG-treated conditions. In leukocyte-depleted cells, the concentration of interleukin (IL)-1 beta decreased 5-fold in comparison with total cell cultures, suggesting that leukocytes are the principal source of IL-1 beta, In summary, the results of the present investigation suggest functional interactions between the immune system and steroidogenic cells of the human corpus luteum.
引用
收藏
页码:1584 / 1589
页数:6
相关论文
共 36 条
[1]   PRODUCTION OF MONOCLONAL ANTIBODIES TO GROUP-A ERYTHROCYTES, HLA AND OTHER HUMAN CELL-SURFACE ANTIGENS - NEW TOOLS FOR GENETIC-ANALYSIS [J].
BARNSTABLE, CJ ;
BODMER, WF ;
BROWN, G ;
GALFRE, G ;
MILSTEIN, C ;
WILLIAMS, AF ;
ZIEGLER, A .
CELL, 1978, 14 (01) :9-20
[2]   A HUMAN-LEUKOCYTE ANTIGEN IDENTIFIED BY A MONOCLONAL-ANTIBODY [J].
BERGER, AE ;
DAVIS, JE ;
CRESSWELL, P .
HUMAN IMMUNOLOGY, 1981, 3 (03) :231-245
[3]  
Best CL, 1996, HUM REPROD, V11, P790
[4]  
BEST CL, 1995, RECENT PROG HORM RES, V50, P387
[5]   ISOLATION OF OVINE LUTEAL CELL SUBPOPULATIONS BY FLOW-CYTOMETRY [J].
BRANNIAN, JD ;
STOUFFER, RL ;
SHIIGI, SM ;
HOYER, PB .
BIOLOGY OF REPRODUCTION, 1993, 48 (03) :495-502
[6]  
BRANNSTROM M, 1994, FERTIL STERIL, V61, P488
[7]  
BRANNSTROM M, 1993, HUM REPROD, V8, P1762
[8]   IS CORPUS-LUTEUM REGRESSION AN IMMUNE-MEDIATED EVENT - LOCALIZATION OF IMMUNE-SYSTEM COMPONENTS AND LUTEINIZING-HORMONE RECEPTOR IN HUMAN CORPORA-LUTEA [J].
BUKOVSKY, A ;
CAUDLE, MR ;
KEENAN, JA ;
WIMALASENA, J ;
UPADHYAYA, NB ;
VANMETER, SE .
BIOLOGY OF REPRODUCTION, 1995, 53 (06) :1373-1384
[9]   ICAM-3 INTERACTS WITH LFA-1 AND REGULATES THE LFA-1/ICAM-1 CELL-ADHESION PATHWAY [J].
CAMPANERO, MR ;
DELPOZO, MA ;
ARROYO, AG ;
SANCHEZMATEOS, P ;
HERNANDEZCASELLES, T ;
CRAIG, A ;
PULIDO, R ;
SANCHEZMADRID, F .
JOURNAL OF CELL BIOLOGY, 1993, 123 (04) :1007-1016
[10]  
Carrasco I, 1996, HUM REPROD, V11, P1609