When American football quarterback Aaron Rodgers told his fans to relax after his team’s poor start one season, little did he know that he was also giving a hair-care tip.
His advice is particularly helpful now, after a long pandemic year. About one-quarter of people who contract COVID-19 experience hair loss six months after the onset of symptoms1, probably because of the systemic shock caused by the ordeal of infection and recovery.
Chronic stress has long been associated with hair loss, but the underlying mechanism that links stress to the dysfunction of hair-follicle stem cells has been elusive. Writing in Nature, Choi et al.2 uncover the connection in mice.
Throughout a person’s lifespan, hair growth cycles through three stages: growth (anagen), degeneration (catagen) and rest (telogen). During anagen, a hair follicle continuously pushes out a growing hair shaft.
During catagen, hair growth stops and the lower portion of the hair follicle shrinks, but the hair (now known as a club hair) remains in place. During telogen,
the club hair remains dormant for some time, eventually falling out. Under severe stress, many hair follicles enter telogen prematurely and the hair quickly falls out.
Hair-follicle stem cells (HFSCs) are located in a region of the hair follicle called the bulge. These cells have a crucial role in governing hair growth by interpreting both internal and external signals.
For example, during telogen, HFSCs are kept in a quiescent state and so do not divide3,4. When hair growth is initiated in the next anagen phase, HFSCs are instructed to divide and produce progenitor cells. These progenitors then begin a journey of differentiation, generating several layers of hair follicles and, ultimately, the hair shaft.
Since HFSCs were identified in the bulge region more than 30 years ago5–7, many regulatory molecules — such as gene-transcription factors and signalling proteins — have been shown to control the cells’ quiescence and activation3,4.
Nearly all of these regulators are produced by either HFSCs or their neighbouring cells, including dermal papilla cells, which usually function as a supportive ‘niche’ for HFSCs8,9. But how systemic conditions such as chronic stress affect the activity of HFSCs is incompletely understood.
To answer this question, Choi and colleagues first tested the role of adrenal glands — which produce stress hormones and constitute a key endocrine organ — in the regulation of hair growth, by surgically removing them from mice.
Telogen phases were much shorter in the hair follicles of these animals (which the team dubbed ADX mice) than in control mice (less than 20 days compared with 60–100 days), and the follicles engaged in hair growth roughly three times as often.
The authors were able to suppress this frequent hair growth and restore the normal hair cycle by feeding the ADX mice corticosterone (a stress hormone normally produced by the animals’ adrenal glands). Interestingly, when they unpredictably applied various mild stressors to normal mice for nine weeks,
they observed elevated corticosterone levels accompanied by reduced hair growth, supporting the idea that corticosterone produced by the adrenal glands during chronic stress inhibits the initiation of hair growth.
How do HFSCs sense corticosterone? Because corticosterone signals through a protein known as the glucocorticoid receptor, selective deletion of this receptor in different cell types in the skin should reveal which cells are required to receive the signal.
Choi et al. found that selective deletion in the dermal papillae blocked the inhibitory effects of corticosterone on hair growth, whereas deletion in HFSCs themselves had no effect. This suggests that HFSCs do not sense the stress hormone directly — and that, instead, the dermal papillae have a crucial role in signal transmission.
To understand how dermal papillae relay the stress signal onwards to HFSCs, the authors profiled the messenger RNAs (which serve as the template for protein production) that are expressed in dermal papillae. This pointed to a secreted protein called growth arrest-specific 6 (GAS6) as a candidate molecular messenger.
Indeed, delivering GAS6 into the skin using an adenovirus vector (a common tool in gene therapy) not only stimulated hair growth in normal mice, but also restored hair growth during chronic stress or corticosterone feeding.
Next, Choi and colleagues found that the protein AXL — a receptor for GAS6 that is expressed by HFSCs — passes the signal on to HFSCs to stimulate cell division.
These and other data generated by the authors show that corticosterone signalling, triggered by chronic stress, leads to inhibition of GAS6 production in dermal papillae, and that forced expression of GAS6 in the dermis can bypass the inhibitory effect of chronic stress on hair growth (Fig. 1).
These exciting findings establish a foundation for exploring treatments for hair loss caused by chronic stress. Before this knowledge can be applied to humans, however, several issues should be carefully examined.
First, although corticosterone is considered to be the rodent equivalent of human cortisol, we do not yet know whether cortisol signals in a similar fashion in humans. Characterization of GAS6 expression in human dermal papillae during the hair-growth cycle, and under stressed conditions, will be one of the first steps to take.
Second, the duration of hair-cycle phases is different in mice and humans. In adult mice, most hair follicles are in the telogen phase at any given time, compared with only around 10% of human hair follicles10. This point is particularly important because, in inhibiting GAS6 production, Choi et al. showed that corticosterone had a role in prolonging telogen.
They did not comprehensively evaluate the anagen phase, which accounts for the status of roughly 90% of follicles in the human scalp. It will be interesting to see whether chronic stress, and perhaps cortisol, can ‘push’ anagen hair follicles into telogen in humans, or whether these factors serve only to prolong telogen, as in mice.
Finally, Choi et al. have shown that GAS6 promotes the expression of several genes involved in cell division in HFSCs, without interfering with known transcription factors and signalling pathways.
So, the authors might have uncovered a previously unknown mechanism that stimulates HFSC activation directly by promoting cell division. In ageing skin, most progenitor cells harbour DNA mutations — including harmful ones that are often found in skin cancers — without forming tumours11.
It will be crucial to see whether forced GAS6 expression could inadvertently unleash the growth potential of these quiescent but potentially mutation-containing HFSCs.
Although further studies are needed, Choi et al. have beautifully uncovered a cellular and molecular mechanism that links stress hormones produced by adrenal glands to the activation of HFSCs through the control of GAS6 expression in dermal papillae.
Moreover, they have shown that injecting GAS6 into the skin can reinitiate hair growth in mice even when the animals are experiencing chronic stress. Modern life for humans is inevitably stressful. But perhaps, one day, it will prove possible to combat the negative impact of chronic stress on our hair, at least — by adding some GAS6.