AI Article Synopsis

  • Muse cells are pluripotent-like stem cells found in bone marrow, peripheral blood, and organ connective tissues, identified by the SSEA-3 marker, though their specifics in extraembryonic tissue are less understood.
  • Human umbilical cord SSEA-3(+) cells show characteristics that resemble early-stage development, expressing pluripotency markers and differentiating efficiently at the single-cell level, unlike adult tissue Muse cells.
  • The discovery that human-UC-SSEA-3(+) cells bear a gene expression profile similar to post-implantation blastocysts, along with their potential for lower differentiation-related DNA methylation, suggests they could serve as important resources for research in human development and reproductive medicine.

Article Abstract

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11335221PMC
http://dx.doi.org/10.1007/s00018-024-05339-4DOI Listing

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Article Synopsis
  • Muse cells are pluripotent-like stem cells found in bone marrow, peripheral blood, and organ connective tissues, identified by the SSEA-3 marker, though their specifics in extraembryonic tissue are less understood.
  • Human umbilical cord SSEA-3(+) cells show characteristics that resemble early-stage development, expressing pluripotency markers and differentiating efficiently at the single-cell level, unlike adult tissue Muse cells.
  • The discovery that human-UC-SSEA-3(+) cells bear a gene expression profile similar to post-implantation blastocysts, along with their potential for lower differentiation-related DNA methylation, suggests they could serve as important resources for research in human development and reproductive medicine.
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Peripheral blood (PB) contains several types of stem/progenitor cells, including hematopoietic stem and endothelial progenitor cells. We identified a population positive for both the pluripotent surface marker SSEA-3 and leukocyte common antigen CD45 that comprises 0.04% ± 0.

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In 2010, Multilineage Differentiating Stress Enduring (Muse) cells were introduced to the scientific community, offering potential resolution to the issue of teratoma formation that plagues both embryonic stem (ES) and induced pluripotent (iPS) stem cells. Isolated from human bone marrow, dermal fibroblasts, adipose tissue and commercially available adipose stem cells (ASCs) under severe cellular stress conditions, Muse cells self-renew in a controlled manner and do not form teratomas when injected into immune-deficient mice. Furthermore, Muse cells express classic pluripotency markers and differentiate into cells from the three embryonic germ layers both spontaneously and under media-specific induction.

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A mystery unraveled: nontumorigenic pluripotent stem cells in human adult tissues.

Expert Opin Biol Ther

July 2014

The University of California, David Geffen School of Medicine, Department of Obstetrics and Gynecology , 10833 Le Conte Ave, Box 951740, Los Angeles, CA 90095-1740 , USA +1 310 206 3670 ;

Introduction: Embryonic stem cells and induced pluripotent stem cells have emerged as the gold standard of pluripotent stem cells and the class of stem cell with the highest potential for contribution to regenerative and therapeutic application; however, their translational use is often impeded by teratoma formation, commonly associated with pluripotency. We discuss a population of nontumorigenic pluripotent stem cells, termed Multilineage Differentiating Stress Enduring (Muse) cells, which offer an innovative and exciting avenue of exploration for the potential treatment of various human diseases.

Areas Covered: This review discusses the origin of Muse cells, describes in detail their various unique characteristics, and considers future avenues of their application and investigation with respect to what is currently known of adult pluripotent stem cells in scientific literature.

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