Differential cellular expression of LIGHT and its receptors in early gestation human placentas

被引:12
作者
Gill, Ryan M.
Coleman, Neil M.
Hunt, Joan S.
机构
[1] Univ Kansas, Med Ctr, Dept Pathol & Lab Med, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA
关键词
human; LIGHT; placenta; LIGHT receptors; TNFSF14; TNF superfamily;
D O I
10.1016/j.jri.2006.08.083
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
LIGHT (homologous to lymphotoxins, exhibits inducible expression, competes with herpes simplex virus glycoprotein D for HVEM. a receptor expressed by T lymphocytes) is an apoptosis-inducing member of the tumor necrosis factor family of ligands. Messenger RNAs encoding LIGHT and its receptors, lymphotoxin-P receptor (I-TOR), decoy receptor-3 (DcR3) and herpes virus entry mediator (HVEM), are present in first trimester and term placentas. Proteins have been localized to specific cells in term but not earlier gestation placentas. Here, we have studied LIGHT and its receptors in early (6-7 weeks) and early-to-middle (8-13 weeks) gestation using immunohistology. Notable cell-specific, gestation-related features were identified. LIGHT and two of its receptors, a membrane-bound receptor that mediates apoptosis (LTPR) and a soluble receptor that interferes with LIGHT signaling (DcR3), were present in syncytiotrophoblast and cytotrophoblast cells in all samples but were detected in placental stromal cells only at week 8 and thereafter. HVEM, a membrane-bound receptor that protects against apoptosis, was expressed only on syncytiotrophoblast. These observations suggest that the LIGHT system may regulate early to middle stages of placental development via cell-specific, temporally programmed expression of the ligand and its receptors, and may also assist in preserving placental immune privilege. (C) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
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页码:1 / 6
页数:6
相关论文
共 22 条
[1]  
Browning JL, 1997, J IMMUNOL, V159, P3288
[2]  
CHEN HL, 1991, AM J PATHOL, V139, P327
[3]   Soluble receptor (DcR3) and cellular inhibitor of apoptosis-2 (cIAP-2) protect human cytotrophoblast cells against LIGHT-mediated apoptosis [J].
Gill, RM ;
Hunt, JS .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 165 (01) :309-317
[4]   Differential expression of LIGHT and its receptors in human placental villi and amniochorion membranes [J].
Gill, RM ;
Ni, J ;
Hunt, JS .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 161 (06) :2011-2017
[5]   Herpesvirus entry mediator ligand (HVEM-L), a novel ligand for HVEM/TR2, stimulates proliferation of T cells and inhibits HT29 cell growth [J].
Harrop, JA ;
McDonnell, PC ;
Brigham-Burke, M ;
Lyn, SD ;
Minton, J ;
Tan, KB ;
Dede, K ;
Spampanato, J ;
Silverman, C ;
Hensley, P ;
DiPrinzio, R ;
Emery, JG ;
Deen, K ;
Eichman, C ;
Chabot-Fletcher, M ;
Truneh, A ;
Young, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (42) :27548-27556
[6]   Tumor necrosis factors: Pivotal components of pregnancy? [J].
Hunt, JS ;
Chen, HL ;
Miller, L .
BIOLOGY OF REPRODUCTION, 1996, 54 (03) :554-562
[7]   Pathophysiology of histological changes in early pregnancy loss [J].
Jauniaux, E ;
Burton, GJ .
PLACENTA, 2005, 26 (2-3) :114-123
[8]   Trophoblastic oxidative stress in relation to temporal and regional differences in maternal placental blood flow in normal and abnormal early pregnancies [J].
Jauniaux, E ;
Hempstock, J ;
Greenwold, N ;
Burton, GJ .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (01) :115-125
[9]   A newly identified member of the tumor necrosis factor receptor superfamily with a wide tissue distribution and involvement in lymphocyte activation [J].
Kwon, BS ;
Tan, KB ;
Ni, J ;
KwiOkOh ;
Lee, ZH ;
Kim, KK ;
Kim, YJ ;
Wang, S ;
Gentz, R ;
Yu, GL ;
Harrop, J ;
Lyn, SD ;
Silverman, C ;
Porter, TG ;
Truneh, A ;
Young, PR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (22) :14272-14276
[10]   LIGHT, a new member of the TNF superfamily, and lymphotoxin α are ligands for herpesvirus entry mediator [J].
Mauri, DN ;
Ebner, R ;
Montgomery, RI ;
Kochel, KD ;
Cheung, TC ;
Yu, GL ;
Ruben, S ;
Murphy, M ;
Eisenberg, RJ ;
Cohen, GH ;
Spear, PG ;
Ware, CF .
IMMUNITY, 1998, 8 (01) :21-30