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What Are Totipotent Stem Cells?


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Stem cellsare characterized according to their degree ofpotency, which refers to their varying ability to differentiate into different cell types. Totipotent cells are the most potent of all stem cells, and defining them is important for research and the field of regenerative medicine.

Definition of totipotent stem cells

There are two definitions of totipotent stem cells, which reflects the inherent technical difficulty that lies in characterizing them1:

  1. A totipotent cell is a single cell that can give rise to a new organism, given appropriate maternal support (most stringent definition)
  2. A totipotent cell is one that can give rise to all extraembryonic tissues, plus all tissues of the body and thegermline(less stringent definition)

The original test of totipotency was performed in mice by Tarkowski (1959)2, who isolated a single blastomere (cells created by divisions of thezygote, consisting of 2–16 cells), placed it into an emptyzona pellucida, and monitored its development into live born young.


This approach is not bulletproof; the failure ofblastomeresto supportchimeradevelopment may indicate limitations related to the reconstructed embryo, rather than restricted development potential of the cell in question.


It is for this reason that the second, less stringent definition of totipotency is also widely used.


Having two definitions inevitably creates confusion, particularly as the term “totipotency” is often used inappropriately in the literature. It has been argued that this creates unnecessary ethical controversy with practical and political implications.3


有时“全能的”这个词是给细胞s if they merely participate in an embryonic process – however, this doesn’t mean that they necessarily could give rise to an organism. Other common causes for misclassification include assuming the expression of early embryonic markers to mean totipotency, and taking partial or superficial resemblance to an embryo as evidence for totipotency.3


Totipotent stem cells differ from pluripotent cells, which can differentiate into cells from any of the three germ layers, and multipotent cells which are less potent. 

Why the fuss about totipotent stem cells?

Totipotent stem cells are unique as they have a greater developmental potential compared with other stem cells. Having the ability to isolate and culture totipotent stem cells creates many therapeutic and research possibilities1related to:
  • Studying zygotic genome activation (the point at which development becomes exclusively controlled by the zygotic genome, rather than the maternal genome)4
  • Rewiring the epigenome (treating pathological conditions induced by epigenetic alterations)5
  • Understanding early embryonic development in more detail
  • Creating human-animalchimeras6(从理论上讲,动物与人体器官可以人工智能d disease modeling, drug development and transplantation)1

Stem cells are increasingly being used as model systems in research. Differentiating between stem cell types relies on an understanding of the embryological roadmaps and the factors that define their pathways.

Source of totipotent stem cells

Thediploid zygotecell is totipotent. Totipotent cells also exist in subsequent divisions of thezygote, before the rise of thetrophectoderm lineage(which occurs approximately four days after fertilization, depending on the species).


To understand the origin of totipotent stem cells, it helps to be familiar with the early stages of embryonic development, and the related terminology.


The table below highlights the important stages of early embryonic development and demonstrates the defining point at which totipotent stem cell no longer exist, and pluripotent cells arise.

Major stages of early embryonic development

A table showing the major stages of early embryonic development

*To provide a unified developmental chronology of mammalian embryology, the Carnegie Institution for Science developed a set of 23 stages known as the “Carnegie stages” whereby stages are defined by morphological development, and not directly by age or size.
**note: the number of cells at compaction varies between mammalian species

When does a totipotent stem cell change?

Totipotent cells cease to exist around the time of the formation of the inner cell mass, when thetrophectoderm lineageis established.1Totipotent stem cells will divide and differentiate to give rise to cells that will develop into one of the three germ layers:

Cell Potency Fate
Epiblast Pluripotent
The epiblast gives rise to the three primary germ layers (ectoderm, endoderm, mesoderm) which will form allsomatic lineagesplus thegermline.
Hypoblast
Not pluripotent, not totipotent
The hypoblast gives rise to the extraembryonicprimitive endoderm,即提供营养th的卵黄囊e embryo when primitive placental circulation has been established.
Trophoblast
Not pluripotent, not totipotent
The trophoblast gives rise to various extraembryonic structures which enable implantation into the uterine wall, secrete human chorionic gonadotropin to enable progesterone secretion from thecorpus luteum, and form the chorion (fetal part of the placenta).

Glossary

Blastomere: Cells created by divisions of thezygote, consisting of 2–16 cells
Chimera:An organism composed of a mixture of different cell populations that derive from more than onezygote(either from the same or different species). Can be formed by different processes, such as the mixing of early embryos or the grafting of tissues from different stages of development.
Corpus luteum:Endocrine structure that develops from an ovarian follicle once the oocyte has been released
Diploid:Having two sets of chromosomes (total of 46 in humans), with one member of each chromosome pair derived from the ovum, and one from the sperm. Ovum and sperm cells are haploid as they each have 23 chromosomes.
Germline:Cells that develop into sperm or oocytes
Primitive endoderm:The yolk sac derived from hypoblasts
Somatic lineages:All cells in the body, excluding the germ cells
Trophectoderm lineage:Cell lineage which gives rise to the trophoblast of the placenta, and provides support to the inner cell mass
Zona pellucida:Extracellular coat that surrounds the mammalian oocyte, crucial for fertilization
Zygote: diploidcell which results from the fusion of a sperm and ovum

Features of totipotent stem cells

Efforts have been made to establish methods to stabilize or create cells with an expanded developmental potential, relative to established lines of embryonic stem cells.

Through this work, typically in mice, researchers have found a few pieces of the totipotency puzzle.7This has partly been achieved by analyzing the gene regulatory network that is active at the earliest stages of mammalian embryogenesis, and screening chemicals for their ability to modulate stem cell gene expression.

As it is impractical to assess totipotency in cells using the aforementioned gold standard in every instance (by transferring a blastomere to an emptyzona pellucida, transferring it to a mother and seeing if it supports the development and birth of live young), some relevant measures and criteria have been established. These methods are based on characteristics specific to early developmental stages:

Gene expression

Gene expression should be characteristic of the appropriate stage of development, e.g.:
  • Genes specific to the two-cell stage have been identified in mice (Zscan4, Dux, Eifa, Zfp352, Tcstv1/3, and Tpodz1–5)1
  • Totipotent cells should lack the key pluripotency genes (Pou5f1, Sox2,andNanoghave been identified in mice)8
  • Oct4, a singular transcription factor, may be indicative of the developmental stage.Oct4is encoded byPOU5F1and belongs to a family of transcription factors which activate the expression of their target genes.Oct4is expressed in germ cells, embryonic stem cells and whole embryos, and expression levels vary dramatically during development. A key role forOct4in embryogenesis has been identified in several species, including humans.9

Chromatin mobility

Chromatin (the complexes of histones and DNA that condense to form chromosomes) mobility is higher in totipotent cells than in pluripotent cells, and chromatin dynamics seem to underlie changes in cellular plasticity.10

Ability to differentiate

Totipotent cells should have the ability to differentiatein vitrointo cells representative of the three embryonic germ layers, as well as the trophectoderm, primitive endoderm and their derivatives.1

Establishment of expanded potential stem cells

It has been noted that while some cells may pass several tests of totipotency, those which are “artificially” induced may not actually have a normal developmental counterpart.


Therefore, a term has been coined to describe cells that retain features of totipotent stem cells: expanded potential stem cells (EPSCs).


EPSCs have been established in mice from individual eight-cell blastomeres, and have also been converted from mouse embryonic stem cells and induced pluripotent stem cells.11This protocol has been described in detail12and the conversion takes approximately 2–3 weeks in each case.


Characterizing totipotent stem cells presents many challenges, and it remains to be seen whether artificially induced totipotent cells could be maintained in isolation.


However, given that other cell lines can be derived from EPSCs, and the huge potential of regenerative medicine in biotechnology and medicine, it is likely that refining the criteria for totipotency will remain a high priority for the field.


References:

  1. Baker, C.L., Pera, M.F. (2018). Capturing Totipotent Stem Cells.Cell Stem Cell22: 25-34
  2. Tarkowski, A. J. K. (1959). Experiments on the development of isolated blastomeres of mouse eggs.Nature184: 1286-1287
  3. Condic, M. L. (2014). Totipotency: What it is and what it is not.Stem Cells and Development23(8):796-812
  4. Schier, A. F. (2007). The maternal-zygotic transition: death and birth of RNAs.Science316: 406-407
  5. Ferrari, A.,et al. (2019). Epigenome modifiers and metabolic rewiring: new frontiers in therapeutics.Pharmacology & Therapeutics193: 178-193
  6. Wu, J.,et al. (2016). Stem cells and interspecies chimaeras.Nature540: 51-59
  7. Yang, Y.,et al. (2017). Derivation of pluripotent stem cells with in vivo embryonic and extraembryonic potency.Cell169: 243-257
  8. Sharov, A. A.,et al. (2008). Identification ofPou5f1,Sox2, andNanogdownstream target genes with statistical confidence by applying a novel algorithm to time course microarray and genome-wide chromatin immunoprecipitation data.BMC Genomics9: 269
  9. Fogarty, N. M. E.et al. (2017). Genome editing reveals a role for OCT4 in human embryogenesis.Nature550:67-73
  10. Bošković, A.,et al. (2014). Higher chromatin mobility supports totipotency and precedes pluripotencyin vivo.Genes & Development28:1042-1047
  11. Yang, J.et al. (2017). Establishment of mouse expanded potential stem cells.Nature550: 393-397
  12. Yang, J.,et al. (2019).In vitroestablishment of expanded potential stem cells from mouse pre-implantation embryos or embryonic stem cells.Nature Protocols14: 350-378
Meet the Author
米歇尔·Trott, PhD
米歇尔·Trott, PhD
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