Abstract

Pluripotent stem cells give rise to reproductively enabled offsprings by generating progressively lineage-restricted multipotent stem cells that would differentiate into lineage-committed stem and progenitor cells. These lineage-committed stem and progenitor cells give rise to all adult tissues and organs. Adult stem and progenitor cells are generated as part of the developmental program and play critical roles in tissue and organ maintenance and/or regeneration. The ability of pluripotent stem cells to self-renew, maintain pluripotency, and differentiate into a multicellular organism is highly dependent on sensing and integrating extracellular and extraorganismal cues. Proteins perform and integrate almost all cellular functions including signal transduction, regulation of gene expression, metabolism, and cell division and death. Therefore, maintenance of an appropriate mix of correctly folded proteins, a pristine proteome, is essential for proper stem cell function. The stem cells' proteome must be pristine because unfolded, misfolded, or otherwise damaged proteins would interfere with unlimited self-renewal, maintenance of pluripotency, differentiation into downstream lineages, and consequently with the development of properly functioning tissue and organs. Understanding how various stem cells generate and maintain a pristine proteome is therefore essential for exploiting their potential in regenerative medicine and possibly for the discovery of novel approaches for maintaining, propagating, and differentiating pluripotent, multipotent, and adult stem cells as well as induced pluripotent stem cells. In this review, we will summarize cellular networks used by various stem cells for generation and maintenance of a pristine proteome. We will also explore the coordination of these networks with one another and their integration with the gene regulatory and signaling networks.

Highlights

  • IntroductionInner cell mass of the embryo gives rise to pluripotent stem cells

  • During early embryogenesis, inner cell mass of the embryo gives rise to pluripotent stem cells

  • The goal of this review is to summarize our current understanding of how stem cell including ESCs, induced pluripotent stem cells (iPSCs), and various adult stem and progenitor cell types generate and maintain a pristine proteome

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Summary

Introduction

Inner cell mass of the embryo gives rise to pluripotent stem cells. Stem Cells International of pluripotent stem cells in giving rise to a fully functional and reproductively enabled offspring as well as ability of the multipotent stem and progenitor cells to maintain tissue homoeostasis requires production and maintenance of an appropriate mix of error-free proteins This is accomplished by coordinated activities of networks responsible for protein synthesis, folding, quality control, and degradation. Maintenance of a pristine proteome becomes critical for pluripotent stem cells’ immortality and for maintenance and proper functioning of adult stem and progenitor cells tasked with forming and maintaining tissues and organs [10,11,12] Because of these reasons, pluripotent stem cells have very low tolerance to the accumulation of damaged, misfolded, and/or aggregated proteins (Figure 1). Unfolded, misfolded, damaged, and/or aggregated proteins are eliminated through the ubiquitin/proteasome system (UPS) or by autophagy-mediated degradation depending on the size of the protein complex and whether they are integral to an organelle (Figure 2) [20,21,22,23]

Protein Folding in the Cytoplasm
Ub activation E2 Ub conjugation E3 Ub ligation
Autophagy
Findings
Concluding Remarks and Future Directions
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