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5 expressed in the epithelial cells, although decidual and embryonic cells also accumulate this mRNA.
6 n expression of NF-kappaB, TNF, and IL-10 in decidual and myometrial macrophages in C57BL/6J mice.
10 the relative contribution and importance of decidual and trophoblast ADA at the maternal-fetal inter
13 ggest therefore that uDCs directly fine-tune decidual angiogenesis by providing two critical factors,
16 nterstitial cytotrophoblasts, we observed in decidual areas containing interstitial cytotrophoblasts
17 ua express strong FasL immunoreactivity, and decidual areas containing interstitial cytotrophoblasts
21 a vital regulatory cascade involving IL-33, decidual B cells and PIBF1 in safeguarding term pregnanc
22 iated stromal cells, and massive breakage of decidual blood vessels, leading to uterine hemorrhage an
23 patterns in the uterine endometrium, at the decidual boundary, in the decidual vasculature, and in t
24 trual endometrium and the mouse uterus after decidual breakdown, evidence that VEGF has pleiotropic e
25 portant for iTreg cell induction, we studied decidual CD14(+) APCs using immunohistochemistry and flo
29 Decidual iNKT cells comprised 0.48% of the decidual CD3+ T cell population, a frequency 10 times gr
30 hird trimester decidua and demonstrated that decidual CD4(+) and CD8(+) T cells exhibit a highly diff
31 usly produce IL-12, whereas freshly isolated decidual CD4(+) T cells expressed high levels of activat
37 B mRNA in decidual EM T cells suggests that decidual CD8(+) T cells pursue alternative means of EM c
38 l sections were immunostained for FKBP51 and decidual cell (DC) and interstitial trophoblast (IT) mar
39 al regulator of the unique ECM that controls decidual cell architecture and differentiation, and it p
40 nized bacteria in the pregnant uterus led to decidual cell death, tissue disintegration, and resorpti
41 suggests that it acts locally and regulates decidual cell development and the endometrial vasculatur
42 L-6 levels in first trimester leukocyte-free decidual cell incubations, as measured by real time quan
43 HtrA1 and HtrA3 are crucial for trophoblast-decidual cell interaction in the control of trophoblast
47 oid receptor (GR), and total and p-ERK1/2 in decidual cells (DCs) and interstitial trophoblasts (IT)
48 ignificantly higher interleukin-6 HSCOREs in decidual cells (DCs) but not in interstitial trophoblast
50 iters, cytomegalovirus replicated in diverse decidual cells and placental trophoblasts and capillarie
53 Thus, secretion of gal1 by dNKs and other decidual cells contributes to the generation of an immun
58 her immunohistochemical staining for IL-6 in decidual cells from preeclamptic versus preterm, gestati
59 to morphologically and functionally distinct decidual cells in a unique process known as decidualizat
60 , addition of exogenous prolactin to primary decidual cells in culture also caused a marked decrease
61 human endometrial stromal cells (HESCs) into decidual cells in response to progesterone, although the
62 (IL-8) was evaluated in leukocyte-free term decidual cells incubated with estradiol (E2; control) or
65 chment, de novo synthesis of estrogen by the decidual cells is critical for stromal differentiation.
67 y, thrombin-enhanced IL-8 expression in term decidual cells may explain how abruption-associated PPRO
68 clusively in luminal epithelial and adjacent decidual cells occurred at implantation sites of hamster
71 ble induction of GPR64 expression in uterine decidual cells points to its potential physiological sig
75 lantation; however, postimplantation uterine decidual cells showed terminal differentiation and senes
76 a 29-kDa protein and localizes to a band of decidual cells surrounding the trophoblast cell layer on
78 may provide important signals to maternal NK decidual cells that interact with trophoblast cells at t
79 e endometrial stromal cells into specialized decidual cells that support the development of the impla
80 nts expression of MMP-1, MMP-3, and MMP-9 in decidual cells to interfere with normal stepwise EVT inv
81 e/paracrine enhancer of sFlt-1 expression by decidual cells to promote pre-eclampsia by interfering w
82 C, IFN-gammaR1, and -R2 to vimentin-positive decidual cells versus cytokeratin-positive interstitial
83 e data, we hypothesize that TGF-beta acts on decidual cells via ALK5 to induce expression of other gr
86 yncytiotrophoblasts, chorionic trophoblasts, decidual cells, and amniotic epithelial cells, as well a
87 tromal cells surrounding the blastocyst into decidual cells, and protection of the "semiallogenic" em
89 ctions between the conceptus and surrounding decidual cells, but the involvement of clock genes in th
90 First trimester human decidua is composed of decidual cells, CD56(bright)CD16(-) decidual natural kil
91 e mice also revealed increased cell death in decidual cells, decreased cell proliferation in undiffer
92 es and differentiates into large epithelioid decidual cells, is critical to the establishment of feta
93 s associated with aberrations in mesometrial decidual cells, mesometrial vascular integrity, and disr
96 d in their abilities to attach to and invade decidual cells, whereas there were no differences with l
97 s, sFlt-1 expression has not been studied in decidual cells, which are the predominant cell type enco
98 induces differentiation of uterine stroma to decidual cells, which regulate embryo-uterine interactio
99 to morphologically and functionally distinct decidual cells, which support embryonic growth and survi
100 cells undergo terminal differentiation into decidual cells, which support the proper progression of
114 rate at which embryos and their surrounding decidual covering became infected, suggesting that intra
115 human glycodelin from first trimester human decidual cytosol by using a rapid two-step high-performa
117 In this study, we tested the hypothesis that decidual defects are an important determinant of the pla
118 l functions necessary for propagating normal decidual development during the post-implantation period
120 with peripheral blood EM CD8(+) T cells, the decidual EM CD8(+) T cells display a significantly reduc
121 ased perforin and granzyme B mRNA content in decidual EM CD8(+) T cells in comparison with peripheral
122 gh levels of perforin and granzyme B mRNA in decidual EM T cells suggests that decidual CD8(+) T cell
126 oRNAs (miRNAs) involved in the regulation of decidual gene expression in human endometrial stromal ce
127 l proliferation with initiation of aperiodic decidual gene expression; uncoupling of these events may
128 ls of LIF-null animals showed no evidence of decidual giant cell formation even by day 6 of pregnancy
131 in placentas obtained after overt abruption (decidual hemorrhage) with or without PPROM and in contro
132 associated with maternal thrombophilias and decidual hemorrhage, which form thrombin from decidual c
133 infection induces placental inflammation and decidual hyperplasia as well as concomitant increase in
135 s hypothesis, we have studied the effects of decidual IGFBP-1 excess on fetoplacental growth in trans
137 icate crosstalk between EVTs, SpA cells, and decidual immune cells that governs their recruitment to
140 th intermediate to high neutralizing titers, decidual infection was suppressed and the placenta was s
142 fferential pattern of cytokine expression by decidual iNKT cells suggests that maternal iNKT cell int
143 ared to their peripheral blood counterparts, decidual iNKT clones were strongly polarized toward gran
145 ituent of the integrin receptors targeted by decidual laminins, also inhibited this differentiation p
146 mice is required for proper formation of the decidual layer and remodeling of the uterine vasculature
147 terus, and is essential for formation of the decidual layer of the placenta and remodeling of the ute
149 ent stages and provide the first evidence of decidual leukocyte involvement in trophoblast-independen
150 mokines in the uterus and their receptors on decidual leukocytes allowed us to identify numerous rece
152 multicolor flow cytometric analyses of human decidual leukocytes detected an elevation in tissue resi
156 , the placenta triggers the development of a decidual lymphatic circulation, which we theorize plays
158 n M1-like macrophages in decidual tissue; 3) decidual M2-like macrophages are reduced in preterm preg
160 this study, two distinct subsets of CD14(+) decidual macrophages (dMs) are found to be present in fi
161 CD14(+)CD163(+)CD206(+)CD209(+) phenotype of decidual macrophages and produced IL-10 and CCL18 but no
162 his observation was confirmed in situ, where decidual macrophages and T cells are continuously expose
163 f human macrophages, including placental and decidual macrophages and used a novel intrauterine infec
165 ies, regardless of the presence of labor; 4) decidual macrophages express high levels of TNF and IL-1
166 Rgamma) during spontaneous preterm labor; 5) decidual macrophages from women who underwent spontaneou
167 G reduces the expression of TNF and IL-12 in decidual macrophages from women who underwent spontaneou
168 d IL-6 levels may contribute to an excess of decidual macrophages implicated in shallow extravillous
169 In vitro phagocytosis assays with human decidual macrophages incubated with pharmacological inhi
170 to determine the mechanisms whereby uterine decidual macrophages phagocytose this bacterium and test
173 cterium and tested the hypothesis that human decidual macrophages use class A scavenger receptors to
174 The amount of these cytokines secreted by decidual macrophages was substantially greater than that
175 retion of M1- and M2-associated cytokines in decidual macrophages, and of proinflammatory cytokines (
176 culture supernatants of human placental and decidual macrophages, identifying them as a major source
177 L14 induced chemotaxis of both dNK cells and decidual macrophages, whereas CXCL6 also induced dNK cel
178 but also induces expression of prolactin, a decidual marker gene, in progestin-treated HESCs without
179 erexpression inhibits the induction of major decidual marker genes, including IGFBP1, WNT4 and PRL.
181 urther showed that Hoxa10 and cyclin D3, two decidual markers, control transcriptional regulation and
182 embrane and laminin 10/11 in the surrounding decidual matrix, suggest that these laminin isoforms inf
183 ion of cytolytic molecules suggests that the decidual microenvironment reduces CD8(+) dT effector res
186 posed of decidual cells, CD56(bright)CD16(-) decidual natural killer (dNK) cells, and macrophages.
189 eceptor 2DS1 (KIR2DS1) expressed by maternal decidual natural killer cells (dNK) and the presence of
190 Cocultures of HLA-G+ EVT with sample matched decidual natural killer cells (dNK), macrophages, and CD
192 educed fusobacterial-induced fetal death and decidual necrosis without affecting the bacterial coloni
193 uption-associated PPROM, we examined whether decidual neutrophil infiltration complicates abruption-a
195 Abruptions were associated with a marked decidual neutrophil infiltration that peaked after PPROM
197 sulted in a 7-fold increase in the number of decidual neutrophils compared with control mice receivin
198 ith peripheral blood neutrophils (PMNs), the decidual neutrophils expressed high levels of neutrophil
200 In contrast to peripheral blood NK cells, decidual NK (dNK) cells lack cytotoxicity, secrete proan
203 e receptor (KIR) genes expressed by maternal decidual NK cells (dNK) and HLA-C genes expressed by fet
204 on site of the fetal-maternal interface, and decidual NK cells have been demonstrated to facilitate e
205 immunoglobulin receptors (KIRs) on maternal decidual NK cells is a key factor in the development of
206 hich involves 1) the activation of cytotoxic decidual NK cells, and 2) the decline of decidual immuno
210 L. monocytogenes infection in primary human decidual organ cultures and in the murine decidua in viv
214 ncy was often complicated by bleeding at the decidual-placental interface and fetal growth retardatio
217 MER39--contribute the enhancer/promoter for decidual prolactin (dPRL), which is dramatically induced
218 o-cAMP revealed a differential regulation of decidual prolactin expression from that of pituitary sug
224 terine stroma is incapable of undergoing the decidual reaction to support further embryonic developme
230 Hysteroscopic assessment indicated a uniform decidual response (confirmed histologically in 40 of 41
232 x) mouse uterus resulted in the absence of a decidual response, confirming that uterine SRC-2 and -1
233 ombinant human BMP2 can partially rescue the decidual response, suggesting that the observed phenotyp
241 man preterm birth, we show here that uterine decidual senescence early in pregnancy via heightened ma
242 ies provide evidence that premature maternal decidual senescence resulting from heightened mTORC1 sig
243 in 53 (p53d/d mice), which exhibit premature decidual senescence that triggers spontaneous and inflam
244 ype mice at midgestation triggered premature decidual senescence utilizing CB1, since administration
246 f spontaneous preterm birth due to premature decidual senescence with increased mTORC1 activity and C
248 vances relevant to intra-amniotic infection, decidual senescence, and breakdown of maternal-fetal tol
249 ntifies a previously unidentified pathway in decidual senescence, which is independent of mTORC1 sign
251 at elevated expression of the T235 allele in decidual spiral arteries may cause first trimester ather
254 sed to human cytomegalovirus (HCMV)-infected decidual stromal cells (DSC), particularly when DSCs exp
255 a and demonstrated that TAP2 is expressed by decidual stromal cells at the maternal-fetal interface.
256 ri-methyl histone H3 lysine 27 (H3K27me3) in decidual stromal cells dictate both elements of pregnanc
257 blood NK cells with conditioned medium from decidual stromal cells mirrored the effects of TGFbeta1.
258 lls when cultured in conditioned medium from decidual stromal cells supplemented with IL-15 and stem
259 l-attracting inflammatory chemokine genes in decidual stromal cells, as evidenced by promoter accrual
265 in part, via its interaction with ILT2, for decidual T cell IL-4 production, known to be crucial for
268 Furthermore, within the same uterus the decidual tissue adjacent to mutant placentas displays ma
269 ow that aPL Abs are specifically targeted to decidual tissue and cause a rapid increase in decidual a
270 the anti-Listeria responses in the maternal decidual tissue are dependent on CSF-1-regulated macroph
272 t heterozygote females expressed EGFP within decidual tissue in locations identical to endogenous Dpr
275 successful implantation via their effects on decidual tissue remodeling, including angiogenesis, and
279 cells have been shown to be concentrated in decidual tissue, where they are able to suppress fetus-s
286 re more abundant than M1-like macrophages in decidual tissue; 3) decidual M2-like macrophages are red
287 ration of activated iNKT-like cells in human decidual tissues is associated with noninfection-related
289 lement induced by aPL antibodies targeted to decidual tissues, rather than by their anticoagulant eff
290 ulation of Fabp4 and Fatp4 in myometrial and decidual tissues, respectively; this suppression was res
292 ession levels than minor allele homozygotes; decidual trophoblasts showed strong CXCR3 immunoreactivi
293 Although increasing evidence supports that decidual (uterine) macrophages and regulatory T cells (T
294 Collectively, these studies identified the decidual uterus as a novel site of E biosynthesis and un
295 during early stages of pregnancy, promoting decidual vascular expansion through VEGF receptor 2 sign
296 ndometrium, at the decidual boundary, in the decidual vasculature, and in the myometrium during pregn
297 athology in SLE patients is characterized by decidual vasculopathy and infarction, and in APLS patien
298 of placental abruption, infarction, hypoxia, decidual vasculopathy, or thrombosis of fetal vessels (n
301 n, at the mesometrial triangle and secondary decidual zone (SDZ) locations, is critical for successfu
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