Abstract

Adult stem cell therapies are increasingly prevalent for the treatment of damaged or diseased tissues, but most of the improvements observed to date are attributed to the ability of stem cells to produce paracrine factors that have a trophic effect on existing tissue cells, improving their functional capacity. It is now clear that this ability to produce trophic factors is a normal and necessary function for some stem cell populations. In vivo adult stem cells are thought to self-renew due to local signals from the microenvironment where they live, the niche. Several niches have now been identified which harbor multiple stem cell populations. In three of these niches – the Drosophila testis, the bulge of the mammalian hair follicle, and the mammalian bone marrow – one type of stem cell has been found to produce factors that contribute to the maintenance of a second stem cell population in the shared niche. In this review, I will examine the architecture of these three niches and discuss the molecular signals involved. Together, these examples establish a new paradigm for stem cell behavior, that stem cells can promote the maintenance of other stem cells.

Highlights

  • The field of stem cell biology has seen numerous studies over the years touting the benefits of stem cell therapies

  • Does this idea that stem cells secrete a “special juice” have anything to do with the normal functioning of stem cell populations? Recent findings in three different adult stem cell niches – the Drosophila testis, the mammalian hair follicle, and the mammalian bone marrow – provide evidence that it does

  • It was originally thought that the two stem cell populations in this niche self-renewed independently from each other, both in response to the secreted cytokine Upd from the hub, which activates Jak/STAT signaling in the stem cell populations

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Summary

Introduction

The field of stem cell biology has seen numerous studies over the years touting the benefits of stem cell therapies. In vivo adult stem cells are thought to self-renew due to local signals from the microenvironment where they live, the niche.

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