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Rab11 family expression in the human placenta: Localization at the maternal-fetal interface.
Taglauer, Elizabeth S; Artemiuk, Patrycja A; Hanscom, Sara R; Lindsay, Andrew J; Wuebbolt, Danielle; Breathnach, Fionnuala M; Tully, Elizabeth C; Khan, Amir R; McCaffrey, Mary W.
Affiliation
  • Taglauer ES; Division of Newborn Medicine, Boston Children's Hospital, Boston, Massachusetts, United States of America.
  • Artemiuk PA; School of Biochemistry and Immunology, Trinity College, Dublin, Ireland.
  • Hanscom SR; Molecular Cell Biology Laboratory, School of Biochemistry and Cell Biology, Biosciences Institute, University College Cork, Cork, Ireland.
  • Lindsay AJ; Molecular Cell Biology Laboratory, School of Biochemistry and Cell Biology, Biosciences Institute, University College Cork, Cork, Ireland.
  • Wuebbolt D; Molecular Cell Biology Laboratory, School of Biochemistry and Cell Biology, Biosciences Institute, University College Cork, Cork, Ireland.
  • Breathnach FM; School of Medicine, Royal College of Surgeons Ireland, Dublin, Ireland.
  • Tully EC; Department of Obstetrics and Gynaecology, Royal College of Surgeons Ireland, Dublin, Ireland.
  • Khan AR; Department of Obstetrics and Gynaecology, Royal College of Surgeons Ireland, Dublin, Ireland.
  • McCaffrey MW; School of Biochemistry and Immunology, Trinity College, Dublin, Ireland.
PLoS One ; 12(9): e0184864, 2017.
Article in En | MEDLINE | ID: mdl-28922401
ABSTRACT
Rab proteins are a family of small GTPases involved in a variety of cellular processes. The Rab11 subfamily in particular directs key steps of intracellular functions involving vesicle trafficking of the endosomal recycling pathway. This Rab subfamily works through a series of effector proteins including the Rab11-FIPs (Rab11 Family-Interacting Proteins). While the Rab11 subfamily has been well characterized at the cellular level, its function within human organ systems is still being explored. In an effort to further study these proteins, we conducted a preliminary investigation of a subgroup of endosomal Rab proteins in a range of human cell lines by Western blotting. The results from this analysis indicated that Rab11a, Rab11c(Rab25) and Rab14 were expressed in a wide range of cell lines, including the human placental trophoblastic BeWo cell line. These findings encouraged us to further analyse the localization of these Rabs and their common effector protein, the Rab Coupling Protein (RCP), by immunofluorescence microscopy and to extend this work to normal human placental tissue. The placenta is a highly active exchange interface, facilitating transfer between mother and fetus during pregnancy. As Rab11 proteins are closely involved in transcytosis we hypothesized that the placenta would be an interesting human tissue model system for Rab investigation. By immunofluorescence microscopy, Rab11a, Rab11c(Rab25), Rab14 as well as their common FIP effector RCP showed prominent expression in the placental cell lines. We also identified the expression of these proteins in human placental lysates by Western blot analysis. Further, via fluorescent immunohistochemistry, we noted abundant localization of these proteins within key functional areas of primary human placental tissues, namely the outer syncytial layer of placental villous tissue and the endothelia of fetal blood vessels. Overall these findings highlight the expression of the Rab11 family within the human placenta, with novel localization at the maternal-fetal interface.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Placenta / Pregnancy Proteins / Gene Expression Regulation, Enzymologic / Rab GTP-Binding Proteins Type of study: Prognostic_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Placenta / Pregnancy Proteins / Gene Expression Regulation, Enzymologic / Rab GTP-Binding Proteins Type of study: Prognostic_studies Limits: Adult / Female / Humans / Pregnancy Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Type: Article Affiliation country: United States