Literature DB >> 27798286

Megalin Is Predominantly Observed in Vesicular Structures in First and Third Trimester Cytotrophoblasts of the Human Placenta.

Tina Storm1, Erik I Christensen1, Julie Nelly Christensen1, Tine Kjaergaard1, Niels Uldbjerg2, Agnete Larsen1, Bent Honoré1, Mette Madsen.   

Abstract

The membrane receptor megalin is crucial for normal fetal development. Besides its expression in the developing fetus, megalin is also expressed in the human placenta. Similar to its established function in the kidney proximal tubules, placental megalin has been proposed to mediate uptake of vital nutrients. However, details of megalin expression, subcellular localization, and function in the human placenta remain to be established. By immunohistochemical analyses of first trimester and term human placenta, we showed that megalin is predominantly expressed in cytotrophoblasts, the highly proliferative cells in placenta. Only limited amounts of megalin could be detected in syncytiotrophoblasts and least in term placenta syncytiotrophoblasts. Immunocytochemical analyses furthermore showed that placental megalin associates with structures of the endolysosomal apparatus. Combined, our results clearly place placental megalin in the context of endocytosis and trafficking of ligands. However, due to the limited expression of megalin in syncytiotrophoblasts, especially in term placenta, it appears that the main role for placental megalin is not to mediate uptake of nutrients from the maternal bloodstream, as previously proposed. In contrast, our results point toward novel and complex functions for megalin in the cytotrophoblasts. Thus, we propose that the perception of placental megalin localization and function should be revised.
© 2016 The Histochemical Society.

Entities:  

Keywords:  cytotrophoblast; endocytosis; endolysosomal system; growth factor signaling; megalin; placenta; syncytiotrophoblast; transmembrane receptor

Mesh:

Substances:

Year:  2016        PMID: 27798286      PMCID: PMC5131744          DOI: 10.1369/0022155416672210

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


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