Chemokine ligand and receptor expression in the pregnant uterus - Reciprocal patterns in complementary cell subsets suggest functional roles

被引:127
作者
Red-Horse, K
Drake, PM
Gunn, MD
Fisher, SJ
机构
[1] Univ Calif San Francisco, Dept Stomatol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[5] Duke Univ, Dept Med, Div Cardiol, Durham, NC USA
关键词
D O I
10.1016/S0002-9440(10)63071-4
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
During human pregnancy, the uterus is infiltrated by a population of maternal leukocytes that co-exist with fetal cytotrophoblasts occupying the decidua and uterine blood vessels. These immune cells, termed "decidual granulated leukocytes," are composed predominately (70%) of the CD56(bright) subset of natural killer cells, accompanied by T cells (15%) and macrophages (15%). The mechanisms underlying the recruitment of these cells are unknown, but by analogy to other systems, chemokines are likely to be involved. We examined the expression patterns of 14 chemokines in the decidualized uterine wall by in situ hybridization, and the expression of chemokine receptors on decidual leukocytes by RNase protection. The striking concordance between the expression of chemokines in the uterus and their receptors on decidual leukocytes allowed us to identify numerous receptor-ligand pairs that may recruit the latter cells to the uterus during pregnancy. Additionally, chemokine expression patterns suggested other, nonimmune functions for these molecules, including a role in cytotrophoblast differentiation. Together, our results imply that chemokine networks serve Important functions at the maternal-fetal interface.
引用
收藏
页码:2199 / 2213
页数:15
相关论文
共 41 条
[1]  
Benirschke K, 2000, PATHOLOGY HUMAN PLAC
[2]   GRANULATED LYMPHOCYTES IN HUMAN ENDOMETRIUM - HISTOCHEMICAL AND IMMUNOHISTOCHEMICAL STUDIES [J].
BULMER, JN ;
MORRISON, L ;
LONGFELLOW, M ;
RITSON, A ;
PACE, D .
HUMAN REPRODUCTION, 1991, 6 (06) :791-798
[3]   Lymphocyte homing and homeostasis [J].
Butcher, EC ;
Picker, LJ .
SCIENCE, 1996, 272 (5258) :60-66
[4]   Unique subpopulations of CD56+ NK and NK-T peripheral blood lymphocytes identified by chemokine receptor expression repertoire [J].
Campbell, JJ ;
Qin, SX ;
Unutmaz, D ;
Soler, D ;
Murphy, KE ;
Hodge, MR ;
Wu, LJ ;
Butcher, EC .
JOURNAL OF IMMUNOLOGY, 2001, 166 (11) :6477-6482
[5]   A study on the density and distribution of uterine Natural Killer cells at mid pregnancy in mice genetically-ablated for CCR2, CCR 5 and the CCR5 receptor ligand, MIP-1α [J].
Chantakru, S ;
Kuziel, WA ;
Maeda, N ;
Croy, BA .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2001, 49 (01) :33-47
[6]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[7]   Chemokines - Chemokines and cell migration in secondary lymphoid organs [J].
Cyster, JG .
SCIENCE, 1999, 286 (5447) :2098-2102
[8]   Trophoblast pseudo-vasculogenesis: faking it with endothelial adhesion receptors [J].
Damsky, CH ;
Fisher, SJ .
CURRENT OPINION IN CELL BIOLOGY, 1998, 10 (05) :660-666
[9]  
DAMSKY CH, 1994, DEVELOPMENT, V120, P3657
[10]   Fas antigen expression on the decidual lymphocytes of pre-eclamptic patients [J].
Darmochwal-Kolarz, D ;
Rolinski, J ;
Leszczynska-Gorzelak, B ;
Oleszczuk, J .
AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2000, 43 (04) :197-201