Key result
Very small embryonic-like stem cells may act as a backup reservoir for adult tissue-committed stem cells.
Key points are not available for this paper at this time.
Answers are grounded in this paper and cite their sources.
Evidence has accumulated that adult hematopoietic tissues and other organs contain a population of dormant stem cells (SCs) that are more primitive than other, already restricted, monopotent tissue-committed SCs (TCSCs). These observations raise several questions, such as the developmental origin of these cells, their true pluripotent or multipotent nature, which surface markers they express, how they can be efficiently isolated from adult tissues, and what role they play in the adult organism. The phenotype of these cells and expression of some genes characteristic of embryonic SCs, epiblast SCs, and primordial germ cells suggests their early-embryonic deposition in developing tissues as precursors of adult SCs. In this review, we will critically discuss all these questions and the concept that small dormant SCs related to migratory primordial germ cells, described as very small embryonic-like SCs, are deposited during embryogenesis in bone marrow and other organs as a backup population for adult tissue-committed SCs and are involved in several processes related to tissue or organ rejuvenation, aging, and cancerogenesis. The most recent results on successful ex vivo expansion of human very small embryonic-like SC in chemically defined media free from feeder-layer cells open up new and exciting possibilities for their application in regenerative medicine.
No takes yet. Share an insight, caveat, or question.
Ratajczak et al. (2017) reported a review. Very small embryonic-like stem cells deposited during embryogenesis in bone marrow and other organs may serve as a backup population for adult tissue-committed stem cells.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: