dc.creatorBorzychowski, AM
dc.creatorChantakru, S
dc.creatorMinhas, K
dc.creatorPaffaro, VA
dc.creatorYamada, AT
dc.creatorHe, H
dc.creatorKorach, KS
dc.creatorCroy, BA
dc.date2003
dc.dateAPR
dc.date2014-11-18T02:06:11Z
dc.date2015-11-26T17:45:17Z
dc.date2014-11-18T02:06:11Z
dc.date2015-11-26T17:45:17Z
dc.date.accessioned2018-03-29T00:27:36Z
dc.date.available2018-03-29T00:27:36Z
dc.identifierPlacenta. W B Saunders Co Ltd, v. 24, n. 4, n. 403, n. 411, 2003.
dc.identifier0143-4004
dc.identifierWOS:000182525500015
dc.identifier10.1053/plac.2002.0924
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/67269
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/67269
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/67269
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1288136
dc.descriptionUterine Natural Killer (uNK) cell differentiation in vivo requires oestrogen (E) priming prior to progesterone (P). Hybridomas between uNK precursor and SP2/0 cells express message for E receptor (ER)alpha but nor PR. However, mature, rodent and human uNK cells lack these receptors. To functionally assess requirements for uNK cell expression of ERalpha, or ERbeta during precursor differentiation, marrow was transplanted from either ERalphadegrees(/)degrees (alphaERKO) or ERbetadegrees(/)degrees (betaERKO) mice into alymphoid RAG-2degrees(/)degrees/gammacdegrees(/)degrees females. Recipients were mated and their implantation sites were examined by light microscopy, morphometry and ultrastructure. High numbers of uNK cells were established from each donor strain. Graft-derived uNK cells were similar in number and morphology to uNK cells of normal mice, suggesting that neither alpha- nor beta-ER is required for uNK precursor cell differentiation. Induction of spiral artery modification in the transplant recipients indicated that graft-derived uNK cells had functional properties. A novel technique for rapid isolation of highly purified uNK cells from normal mice using Dolichos biflorus agglutinin (DBA) lectin-conjugated magnetic beads was employed to obtain RNA. Expression of alpha- and beta-ER was absent by RT-PCR from NK cells isolated from the uterus, supporting the conclusions from the in vivo study. (C) 2003 Elsevier Science Ltd. All rights reserved.
dc.description24
dc.description4
dc.description403
dc.description411
dc.languageen
dc.publisherW B Saunders Co Ltd
dc.publisherLondon
dc.publisherInglaterra
dc.relationPlacenta
dc.relationPlacenta
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectMetrial Gland-cells
dc.subjectInterferon-gamma Contributes
dc.subjectMessenger Ribonucleic-acids
dc.subjectPregnant Mouse Uterus
dc.subjectEstrogen-receptor
dc.subjectMenstrual-cycle
dc.subjectGrowth-factor
dc.subjectMice
dc.subjectProgesterone
dc.subjectDifferentiation
dc.titleFunctional analysis of murine uterine natural killer cells genetically devoid of oestrogen receptors
dc.typeArtículos de revistas


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