Human post-implantation blastocyst-like characteristics of Muse cells isolated from human umbilical cord.
Yoshihiro KushidaYo OgumaKana AbeTaichi DeguchiFederico Girolamo BarberaNoriyuki NishimuraKazumichi FujiokaSota IwataniMari DezawaPublished in: Cellular and molecular life sciences : CMLS (2024)
Muse cells, identified as cells positive for the pluripotent surface marker SSEA-3, are pluripotent-like endogenous stem cells located in the bone marrow (BM), peripheral blood, and organ connective tissues. The detailed characteristics of SSEA-3(+) cells in extraembryonic tissue, however, are unknown. Here, we demonstrated that similar to human-adult tissue-Muse cells collected from the BM, adipose tissue, and dermis as SSEA-3(+), human-umbilical cord (UC)-SSEA-3(+) cells express pluripotency markers, differentiate into triploblastic-lineage cells at a single cell level, migrate to damaged tissue, and exhibit low telomerase activity and non-tumorigenicity. Notably, ~ 20% of human-UC-SSEA-3(+) cells were negative for X-inactive specific transcript (XIST), a naïve pluripotent stem cell characteristic, whereas all human adult tissue-Muse cells are XIST-positive. Single-cell RNA sequencing revealed that the gene expression profile of human-UC-SSEA-3(+) cells was more similar to that of human post-implantation blastocysts than human-adult tissue-Muse cells. The DNA methylation level showed the same trend, and notably, the methylation levels in genes particularly related to differentiation were lower in human-UC-SSEA-3(+) cells than in human-adult tissue-Muse cells. Furthermore, human-UC-SSEA-3(+) cells newly express markers specific to extraembryonic-, germline-, and hematopoietic-lineages after differentiation induction in vitro whereas human-adult tissue-Muse cells respond only partially to the induction. Among various stem/progenitor cells in living bodies, those that exhibit properties similar to post-implantation blastocysts in a naïve state have not yet been found in humans. Easily accessible human-UC-SSEA-3(+) cells may be a valuable tool for studying early-stage human development and human reproductive medicine.
Keyphrases
- induced apoptosis
- endothelial cells
- cell cycle arrest
- stem cells
- induced pluripotent stem cells
- adipose tissue
- dna methylation
- single cell
- bone marrow
- pluripotent stem cells
- mesenchymal stem cells
- cell death
- peripheral blood
- type diabetes
- umbilical cord
- genome wide
- metabolic syndrome
- dna damage
- insulin resistance
- locally advanced
- young adults
- transcription factor