Cellular Complexity of Hemochorial Placenta: Stem Cell Populations, Insights from scRNA-seq, and SARS-CoV-2 Susceptibility.
Cellular Complexity of Hemochorial Placenta: Stem Cell Populations, Insights from scRNA-seq, and SARS-CoV-2 Susceptibility.
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DOI:
10.1007/s40778-021-00194-6
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发表时间:
2021
影响因子:
1.4
通讯作者:
Wallingford MC
中科院分区:
文献类型:
--
作者:
Mallery CS Jr;Carrillo M;Mei A;Correia-Branco A;Kashpur O;Wallingford MC
The placenta is a transient organ that forms de novo and serves a critical role in supporting fetal growth and development. Placental oxygen, nutrients, and waste are transported through processes that depend on vascular structure and cell type-specific expression and localization of membrane transporters. Understanding how the placenta develops holds great significance for maternal–fetal medicine. The purpose of this review is to examine current information regarding placental progenitor populations. Recent advancements in single-cell RNA sequencing (scRNA-seq) provide unprecedented depth for the investigation of cell type-specific gene expression patterns in the placenta. Thus far, several mouse placenta scRNA-seq studies have been conducted which produced and analyzed transcriptomes of placental progenitors and cells of the fully developed placenta between embryonic day (E) 7.0 and E12.5. Together with human placenta scRNA-seq data which, in part, has been produced through coordinated research campaigns in the scientific community to understand the potential for SARS-CoV-2 infection, these mammalian studies lend fundamental insight into the cellular and molecular composition of hemochorial placentae found in both mouse and human. Single-cell placenta research has advanced understanding of tissue-resident stem cells and molecules that are poised to support maternal–fetal communication and nutrient transport. Herein, we provide context for these recent findings by reviewing placental anatomy and cell populations, and discuss recent scRNA-seq mouse placenta findings. Further research is needed to evaluate the utility of placental stem cells in the development of new therapeutic approaches for the treatment of wound healing and disease.
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DOI:
10.3791/54150
发表时间:
2016-06-17
期刊:
Journal of visualized experiments : JoVE
影响因子:
--
作者:
Fang JS;Gritz EC;Marcelo KL;Hirschi KK
通讯作者:
Hirschi KK
DOI:
10.1530/rep-20-0231
发表时间:
2020-12
期刊:
Reproduction (Cambridge, England)
影响因子:
--
作者:
Li H;Huang Q;Liu Y;Garmire LX
通讯作者:
Garmire LX
影响因子:
7.1
作者:
Cui, D.;Liu, Y.;Yang, H.
通讯作者:
Yang, H.
影响因子:
64.8
作者:
Dickinson ME;Flenniken AM;Ji X;Teboul L;Wong MD;White JK;Meehan TF;Weninger WJ;Westerberg H;Adissu H;Baker CN;Bower L;Brown JM;Caddle LB;Chiani F;Clary D;Cleak J;Daly MJ;Denegre JM;Doe B;Dolan ME;Edie SM;Fuchs H;Gailus-Durner V;Galli A;Gambadoro A;Gallegos J;Guo S;Horner NR;Hsu CW;Johnson SJ;Kalaga S;Keith LC;Lanoue L;Lawson TN;Lek M;Mark M;Marschall S;Mason J;McElwee ML;Newbigging S;Nutter LM;Peterson KA;Ramirez-Solis R;Rowland DJ;Ryder E;Samocha KE;Seavitt JR;Selloum M;Szoke-Kovacs Z;Tamura M;Trainor AG;Tudose I;Wakana S;Warren J;Wendling O;West DB;Wong L;Yoshiki A;International Mouse Phenotyping Consortium;Jackson Laboratory;Infrastructure Nationale PHENOMIN, Institut Clinique de la Souris (ICS);Charles River Laboratories;MRC Harwell;Toronto Centre for Phenogenomics;Wellcome Trust Sanger Institute;RIKEN BioResource Center;MacArthur DG;Tocchini-Valentini GP;Gao X;Flicek P;Bradley A;Skarnes WC;Justice MJ;Parkinson HE;Moore M;Wells S;Braun RE;Svenson KL;de Angelis MH;Herault Y;Mohun T;Mallon AM;Henkelman RM;Brown SD;Adams DJ;Lloyd KC;McKerlie C;Beaudet AL;Bućan M;Murray SA
通讯作者:
Murray SA
DOI:
10.18632/aging.104015
发表时间:
2020-10-26
期刊:
Aging
影响因子:
--
作者:
Lü M;Qiu L;Jia G;Guo R;Leng Q
通讯作者:
Leng Q