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Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation
BACKGROUND: Proper placentation, including trophoblast differentiation and function, is essential for the health and well-being of both the mother and baby throughout pregnancy. Placental abnormalities that occur during the early stages of development are thought to contribute to preeclampsia and ot...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218487/ https://www.ncbi.nlm.nih.gov/pubmed/34154587 http://dx.doi.org/10.1186/s12915-021-01056-7 |
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author | Rosenkrantz, Jimi L. Gaffney, Jessica E. Roberts, Victoria H. J. Carbone, Lucia Chavez, Shawn L. |
author_facet | Rosenkrantz, Jimi L. Gaffney, Jessica E. Roberts, Victoria H. J. Carbone, Lucia Chavez, Shawn L. |
author_sort | Rosenkrantz, Jimi L. |
collection | PubMed |
description | BACKGROUND: Proper placentation, including trophoblast differentiation and function, is essential for the health and well-being of both the mother and baby throughout pregnancy. Placental abnormalities that occur during the early stages of development are thought to contribute to preeclampsia and other placenta-related pregnancy complications. However, relatively little is known about these stages in humans due to obvious ethical and technical limitations. Rhesus macaques are considered an ideal surrogate for studying human placentation, but the unclear translatability of known human placental markers and lack of accessible rhesus trophoblast cell lines can impede the use of this animal model. RESULTS: Here, we performed a cross-species transcriptomic comparison of human and rhesus placenta and determined that while the majority of human placental marker genes (HPGs) were similarly expressed, 952 differentially expressed genes (DEGs) were identified between the two species. Functional enrichment analysis of the 447 human-upregulated DEGs, including ADAM12, ERVW-1, KISS1, LGALS13, PAPPA2, PGF, and SIGLEC6, revealed over-representation of genes implicated in preeclampsia and other pregnancy disorders. Additionally, to enable in vitro functional studies of early placentation, we generated and thoroughly characterized two highly pure first trimester telomerase (TERT) immortalized rhesus trophoblast cell lines (iRP-D26 and iRP-D28A) that retained crucial features of isolated primary trophoblasts. CONCLUSIONS: Overall, our findings help elucidate the molecular translatability between human and rhesus placenta and reveal notable expression differences in several HPGs and genes implicated in pregnancy complications that should be considered when using the rhesus animal model to study normal and pathological human placentation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01056-7. |
format | Online Article Text |
id | pubmed-8218487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82184872021-06-23 Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation Rosenkrantz, Jimi L. Gaffney, Jessica E. Roberts, Victoria H. J. Carbone, Lucia Chavez, Shawn L. BMC Biol Research Article BACKGROUND: Proper placentation, including trophoblast differentiation and function, is essential for the health and well-being of both the mother and baby throughout pregnancy. Placental abnormalities that occur during the early stages of development are thought to contribute to preeclampsia and other placenta-related pregnancy complications. However, relatively little is known about these stages in humans due to obvious ethical and technical limitations. Rhesus macaques are considered an ideal surrogate for studying human placentation, but the unclear translatability of known human placental markers and lack of accessible rhesus trophoblast cell lines can impede the use of this animal model. RESULTS: Here, we performed a cross-species transcriptomic comparison of human and rhesus placenta and determined that while the majority of human placental marker genes (HPGs) were similarly expressed, 952 differentially expressed genes (DEGs) were identified between the two species. Functional enrichment analysis of the 447 human-upregulated DEGs, including ADAM12, ERVW-1, KISS1, LGALS13, PAPPA2, PGF, and SIGLEC6, revealed over-representation of genes implicated in preeclampsia and other pregnancy disorders. Additionally, to enable in vitro functional studies of early placentation, we generated and thoroughly characterized two highly pure first trimester telomerase (TERT) immortalized rhesus trophoblast cell lines (iRP-D26 and iRP-D28A) that retained crucial features of isolated primary trophoblasts. CONCLUSIONS: Overall, our findings help elucidate the molecular translatability between human and rhesus placenta and reveal notable expression differences in several HPGs and genes implicated in pregnancy complications that should be considered when using the rhesus animal model to study normal and pathological human placentation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01056-7. BioMed Central 2021-06-21 /pmc/articles/PMC8218487/ /pubmed/34154587 http://dx.doi.org/10.1186/s12915-021-01056-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Rosenkrantz, Jimi L. Gaffney, Jessica E. Roberts, Victoria H. J. Carbone, Lucia Chavez, Shawn L. Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title | Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title_full | Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title_fullStr | Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title_full_unstemmed | Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title_short | Transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
title_sort | transcriptomic analysis of primate placentas and novel rhesus trophoblast cell lines informs investigations of human placentation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8218487/ https://www.ncbi.nlm.nih.gov/pubmed/34154587 http://dx.doi.org/10.1186/s12915-021-01056-7 |
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