The effect of human amniotic epithelial cell on dendritic cell differentiation of peripheral blood monocytes: An experimental study
Background: The amniotic membrane plays an important role in maintaining a healthy pregnancy. The main population cells from amniotic membrane include human amnion epithelial cells (hAECs) which have been shown to possess immunomodulatory properties. Objective: The proximity of hAECs with monocyte l...
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Published in | Iranian journal of reproductive medicine Vol. 18; no. 6 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Research and Clinical Center for Infertility, Shahid Sadoughi University of Medical Sciences of Yazd
17.07.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Background: The amniotic membrane plays an important role in
maintaining a healthy pregnancy. The main population cells from
amniotic membrane include human amnion epithelial cells (hAECs) which
have been shown to possess immunomodulatory properties. Objective: The
proximity of hAECs with monocyte leads to the generation of
tollerogenic dendritic cells. Materials and Methods: hAECs were
obtained from normal pregnancy. Peripheral blood monocytes were
isolated by anti-CD14 MACS method. Co-cultures of monocytes and hAECs
were established in Transwell chambers supplemented with
granulocyte-macrophage colony-stimulating factor (GM-CSF) and
interleukin-4 (IL-4) in the absence and presence of lipopolysaccharide
(LPS) to produce immature and mature DCs, respectively.
Immunophenotyping of the obtained DCs was done through flow cytometry
and the production of cytokines was measured by ELISA. Mixed leukocyte
Reaction (MLR) was also performed for the functional assessment of DCs.
Results: Immunophenotyping of [hAECs - Immature DC (iDC)] and [hAECs -
iDC] + LPS cells revealed that the expression of CD1a, CD80, CD86,
CD40, HLA-DR, and CD83 markers showed no significant difference as
compared with the control group (iDCs and mDCs alone). In the
[hAECs-iDCs] + LPS cells, the percentage of CD14 cells at the ratio of
1:2.5 showed significant differences compared to the control group. The
production of IL-10 and IL-12 showed no significant difference in any
of the cultures as compared to the control groups. Also, co-cultured
DCs did not inhibit proliferation of lymphocyte. Conclusion: Our
findings show that factors secreted from cultured hAECs are unable to
generate of tollerogenic dendritic cells. To achieve a better
understanding of other mechanisms more investigations are needed. |
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ISSN: | 1680-6433 |