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| Indexado |
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| DOI | 10.1016/J.AJOG.2024.12.032 | ||||
| Año | 2025 | ||||
| Tipo | revisión |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
The maternal-fetal interface represents a critical site of immunological interactions that can greatly influence pregnancy outcomes. The unique cellular composition and cell-cell interactions taking place within these tissues has spurred substantial research efforts focused on the maternal-fetal interface. With the recent advent of single-cell technologies, multiple investigators have applied such methods to gain an unprecedented level of insight into maternal-fetal communication. Here, we provide an overview of the dynamic cellular composition and cell-cell communications at the maternal-fetal interface as reported by single-cell investigations. By primarily focusing on data from pregnancies in the second and third trimesters, we aim to showcase how single-cell technologies have bolstered the foundational understanding of each cell's contribution to physiologic gestation. Indeed, single-cell technologies have enabled the examination of classical placental cells, such as the trophoblast, as well as uncovered new roles for structural cells now recognized as active participants in pregnancy and parturition, such as decidual and fetal stromal cells, which are reviewed herein. Furthermore, single-cell data investigating the ontogeny, function, differentiation, and interactions among immune cells present at the maternal-fetal interface, namely macrophages, T cells, dendritic cells, neutrophils, mast cells, innate lymphoid cells, natural killer cells, and B cells are discussed in this review. Moreover, a key output of single-cell investigations is the inference of cell-cell interactions, which has been leveraged to not only dissect the intercellular communications within specific tissues but also between compartments such as the decidua basalis and placental villi. Collectively, this review emphasizes the ways by which single-cell technologies have expanded the understanding of cell composition and cellular processes underlying pregnancy in mid-to-late gestation at the maternal-fetal interface, which can prompt their continued application to reveal new pathways and targets for the treatment of obstetrical disease.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Levenson, Dustyn | - |
WASHINGTON UNIV - Estados Unidos
Wayne State Univ - Estados Unidos Washington University School of Medicine in St. Louis - Estados Unidos Wayne State University School of Medicine - Estados Unidos |
| 2 | ROMERO-GALUE, ROBERTO JOSE | Hombre |
Eunice Kennedy Shriver Natl Inst Child Hlth & Huma - Estados Unidos
UNIV MICHIGAN - Estados Unidos Michigan State Univ - Estados Unidos National Institute of Child Health and Human Development (NICHD) - Estados Unidos University of Michigan Medical School - Estados Unidos MSU College of Human Medicine - Estados Unidos |
| 3 | Miller, Derek | - |
WASHINGTON UNIV - Estados Unidos
Washington University School of Medicine in St. Louis - Estados Unidos |
| 4 | Galaz, Jose | - |
Pontificia Universidad Católica de Chile - Chile
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| 5 | Garcia-Flores, Valeria | - |
WASHINGTON UNIV - Estados Unidos
Washington University School of Medicine in St. Louis - Estados Unidos |
| 6 | Neshek, Barbara | - |
Wayne State Univ - Estados Unidos
Wayne State University School of Medicine - Estados Unidos |
| 7 | Pique-Regi, Roger | - |
Wayne State Univ - Estados Unidos
Wayne State University School of Medicine - Estados Unidos |
| 8 | Gomez-Lopez, Nardhy | - |
WASHINGTON UNIV - Estados Unidos
Washington University School of Medicine in St. Louis - Estados Unidos |
| Fuente |
|---|
| National Institutes of Health |
| Eunice Kennedy Shriver National Institute of Child Health and Human Development |
| National Institute of Allergy and Infectious Diseases |
| School of Medicine, Wayne State University |
| U.S. Department of Health and Human Services |
| Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research |
| Department of Physiology |
| Division of Obstetrics and Maternal-Fetal Medicine , Division of Intramural Research |
| Next Gen Pregnancy Initiative Burroughs Wellcome Fund |
| Agradecimiento |
|---|
| D.L. is supported by the Department of Physiology , Wayne State University School of Medicine . R.R. is supported by the Pregnancy Research Branch (PRB), Division of Obstetrics and Maternal-Fetal Medicine , Division of Intramural Research , Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health , U.S. Department of Health and Human Services (NICHD/NIH/DHHS). N.G-L. is supported by a grant from the National Institute of Allergy and Infectious Diseases, National Institutes of Health ( RAI184481A ) and the Next Gen Pregnancy Initiative Burroughs Wellcome Fund ( 1263500 ). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. |