“Deciphering the mechanisms behind stem cell differentiation advances our understanding of how adult stem cells can be used to maintain tissue integrity and heal wounds,” says Chiung-Ying Chang, a graduate student in the Laboratory of Elaine Fuchs, Rebecca C. Lancefield Professor at Rockefeller.
Adult stem cells are found throughout the body and, like embryonic stem cells, can self-renew indefinitely, forming new cells for the organ in which they reside and aiding in the repair of damaged tissue. In the hair follicle, stem cells come in two types: hair follicle stem cells, which help the hair to grow, and melanocyte stem cells, which give it color.
Fuchs’ research team knew that these two stem cell populations share a niche, a microenvironment that interacts with stem cells and influences their fate inside the hair follicles. In a paper published in Nature in February, they discovered a working relationship between the stem cells that allows hair to be pigmented.
Chang examined the role of nuclear factor I/B (NFIB), a transcription factor that controls gene expression in the hair follicle stem cells. The lab created so-called knockout mice whose hair follicle stem cells were missing the gene Nfib and watched to see what would happen. At first it seemed like not much — the hair on the mice grew like it normally would. But upon closer inspection, Chang found that surprisingly, the melanocyte stem cell behavior had gone awry. Even though the melanocyte stem cells weren’t directly affected by the NFIB knockout, the mice had more of these pigment-producing cells and the cells were differentiating faster than they did in the normal hair cycle. Over the course of many months the knockout mice also showed dark spots of pigment around the hair follicle, visible to the naked eye.
It seemed that NFIB acts as a mediator in the crosstalk between hair follicle stem cells and melanocytes — controlling the timing and number of melanocytes through the action of the hair follicle stem cells. The next question was how, exactly?
Through techniques known as ChIP-sequencing and transcriptional profiling the group determined that NFIB was working through a gene called endothelin-2, and showed that hair follicle stem cells that were missing NFIB had more endothelin-2 protein. NFIB appears to have an effect on the hair cycle, a process whereby the hair follicle goes from dormant to having its stem cells activated, making the hair grow. NFIB was found to limit the amount of endothelin-2 secreted while the niche is resting, keeping endothelin-2 from spurring the melanocyte stem cells to differentiate too early — before the hair starts to grow again.
“What we learned was that NFIB acts as a governor over this process of hair regeneration and pigmentation,” says Chang. “It keeps the hair follicle and melanocyte stem cells working in synchrony to maintain the process.”
“Before Chiung-Ying’s findings, researchers knew how stem cells became activated together, but they didn’t know how they remain silent for prolonged periods of time,” says Fuchs. “Also important is Chiung-Ying’s discovery of how the activities of the two stem cells can be uncoupled, since only melanocyte stem cells respond to endothelin-2.”
The scientists state that synchrony between the two types of cells can come unhinged in a number of stress or disease conditions. In future research they hope to address whether changes in Nfib expression may play an important signaling role in these conditions, noting that situations like UV exposure, where the synchrony is disrupted, are correlated with an increase in endothelin-2.
|Nature online: February 6, 2013
NFIB is a governor of epithelial–melanocyte stem-cell behavior in a shared niche
Chiung-Ying Chang, H. Amalia Pasolli, Eugenia G. Giannopoulou, Geraldine Guasch, Richard M. Gronostajski, Olivier Elemento and Elaine Fuchs