characterization of the conditioned medium from amniotic membrane cells prostaglandins as key effectors of its immunomodulatory activity描述从羊膜细胞条件培养液的前列腺素的关键效应物免疫调节活动.pdfVIP
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characterization of the conditioned medium from amniotic membrane cells prostaglandins as key effectors of its immunomodulatory activity描述从羊膜细胞条件培养液的前列腺素的关键效应物免疫调节活动
Characterization of the Conditioned Medium from
Amniotic Membrane Cells: Prostaglandins as Key
Effectors of Its Immunomodulatory Activity
1,2 1 1 3 1
Daniele Rossi , Stefano Pianta , Marta Magatti , Peter Sedlmayr , Ornella Parolini *
1 Centro di Ricerca E. Menni, Fondazione Poliambulanza-Istituto Ospedaliero, Brescia, Italia, 2 Doctoral School of Molecular Medicine, University of Milan, Milano, Italia,
3 Institute of Cell Biology, Histology and Embryology, Center for Molecular Medicine, Medical University of Graz, Graz, Austria
Abstract
We previously demonstrated that cells isolated from the mesenchymal region of the human amniotic membrane (human
amniotic mesenchymal tissue cells, hAMTC) possess immunoregulatory roles, such as inhibition of lymphocyte proliferation
and cytokine production, and suppression of generation and maturation of monocyte-derived dendritic cells, as reported
for MSC from other sources. The precise factors and mechanisms responsible for the immunoregulatory roles of hAMTC
remain unknown. In this study, we aimed to identify the soluble factors released by hAMTC and responsible for the anti-
proliferative effect on lymphocytes, and the mechanisms underlying their actions, in vitro. Conditioned medium (CM) was
prepared under routine culture conditions from hAMTC (CM-hAMTC) and also from fragments of the whole human amniotic
membrane (CM-hAM). We analyzed the thermostability, chemical nature, and the molecular weight of the factors likely
responsible for the anti-proliferative effects. We also evaluated the participation of cytokines known to be involved in the
immunomodulatory actions of MSC from other sources, and attempted to block different synthetic pathways. We
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