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Development of an Insert Co-culture System of Two Cellular Types in the Absence of Cell-Cell Contact
Published on: July 17, 2016
Somatic cell transformation into stem cell-like cells induced by different microenvironments
Jeong Mook Lim1, Seung Pyo Gong2
1Department of Agricultural Biotechnology; Seoul National University; Seoul, Korea; WCU Biomodulation Program; Seoul National University; Seoul, Korea.
Abstract:
Development of induced pluripotent stem cell (iPSC) technology introduced a novel way to derive pluripotent stem cells, but the genetic manipulation required to generate iPSCs may lead to uncontrolled tumorigenesis of the established cells and thus limit clinical feasibility of the technology. Numerous attempts have been made to date, and alternative reprogramming of somatic cells to reactivate cellular plasticity after differentiation has been suggested. As a result, it had become clear that cell-to-cell interactions and specific acellular environments can be utilized for somatic cell reprogramming. In our previous studies, embryonic stem cell (ESC)-like cells could be derived from transforming ovarian cells and fetal fibroblasts by cell-to-cell interaction or specific cell-mediated microenvironmental factor(s). This cellular event was induced without undertaking genetic manipulation of progenitor cells. Several differences were found between the cellular properties of niche-induced, ESC-like cells and those of genetically manipulated iPSCs and the referenced ESCs. Thus, we provided evidence that terminally differentiated somatic cells either acquire pluripotency-like activity or possess cellular and genetic plasticity under a specific microenvironment and/or cell-to-cell interaction. In this minireview, we discuss derivation of stem cell-like cells under specific microenvironmental conditions in terms of technical perspectives and limitations.
Insights
Generating stem cell-like cells without genetic manipulation is possible. Specific microenvironments and cell-to-cell interactions can induce pluripotency in differentiated somatic cells, offering a safer alternative to induced pluripotent stem cells (iPSCs).
Area of Science:
- Stem Cell Biology
- Regenerative Medicine
- Cellular Reprogramming
Background:
- Induced pluripotent stem cell (iPSC) technology faces challenges with genetic manipulation and potential tumorigenesis, limiting clinical applications.
- Alternative methods for somatic cell reprogramming are being explored to overcome these limitations.
- Cell-to-cell interactions and specific microenvironments show promise for inducing cellular plasticity.
Purpose of the Study:
- To review the derivation of stem cell-like cells using microenvironmental conditions.
- To discuss the technical perspectives and limitations of non-genetic reprogramming methods.
- To highlight the potential of niche-induced stem cell-like cells as an alternative to iPSCs.
Main Methods:
- Review of previous studies on cell-to-cell interactions and microenvironmental factors for somatic cell reprogramming.
- Analysis of cellular properties of niche-induced, ESC-like cells compared to iPSCs and ESCs.
- Discussion of technical aspects and limitations of deriving stem cell-like cells without genetic manipulation.
Main Results:
- Embryonic stem cell (ESC)-like cells can be derived from somatic cells (ovarian cells, fetal fibroblasts) via cell-cell interaction or microenvironmental factors.
- This process does not require genetic manipulation of progenitor cells.
- Niche-induced ESC-like cells exhibit distinct properties compared to genetically manipulated iPSCs and standard ESCs.
- Terminally differentiated somatic cells can acquire pluripotency-like activity or plasticity under specific conditions.
Conclusions:
- Specific microenvironments and cell-to-cell interactions can induce pluripotency-like activity in differentiated somatic cells without genetic manipulation.
- This approach offers a potentially safer alternative to iPSC technology by avoiding genetic modification.
- Further research into technical perspectives and limitations is needed for clinical feasibility.
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