The effect of plucking hairs during different phases of the follicular cycle

Development ◽  
1964 ◽  
Vol 12 (3) ◽  
pp. 465-474
Author(s):  
Elizabeth Johnson ◽  
F. J. Ebling

Hair growth is intermittent; periods of activity when the follicle is producing the hair alternating with periods of rest when the dead hair is retained. In the rat, hair growth occurs in a series of waves which start ventrally and pass over the flanks to the back (Dry, 1926; Butcher, 1934; Johnson, 1958). It has long been known (Collins, 1918; David, 1934) that if hairs are pulled out of resting follicles activity is induced. To explain this phenomenon, Chase (1955) put forward the view that an inhibitor accumulates in the hair follicle during active growth and is dissipated during the resting stage. Plucking during the resting stage removes this inhibitor along with the club hair, so that activity recommences. Preliminary observations on rats with plucked follicles indicated that the response to plucking varied at different stages of the hair cycle. A detailed study seemed desirable, therefore, in order to test more closely than hitherto the validity of the inhibitor hypothesis.

2020 ◽  
Vol 10 (14) ◽  
pp. 4996
Author(s):  
Nicole Braun ◽  
Ulrike Heinrich

Hair plays a major role in perception within a society. It provides information about gender, age, health, and social status. It is therefore not surprising that those affected are exposed to great suffering due to the widespread occurrence of hair loss. As a result, the demand for new products to remedy this problem is not diminishing. Hair grows in cycles, and a hair follicle goes through several phases called the hair cycle. The active growth phase (anagen phase) lasts 2–6 years. In this state a hair follicle shows a growth of about 1 cm per month. In order to improve the existing hair status, hair should be kept in the active anagen phase as long as possible, or the transition to anagen should be stimulated. A number of reviews already describe the influence of individual active ingredients on hair growth. However, the following review describes existing studies of complex dietary supplements with their experimental weaknesses and strengths and their influence on hair loss. Also, for the determination of hair loss, it is important to use a valid method with high acceptance by the test persons. In this context, the TrichoScale® is a validated and non-invasive tool for quantifying hair loss/hair growth. Thus, it is an ideal measuring instrument to objectively quantify the effectiveness of a hair loss treatment.


2020 ◽  
Vol 6 (30) ◽  
pp. eaba1685 ◽  
Author(s):  
Shiqi Hu ◽  
Zhenhua Li ◽  
Halle Lutz ◽  
Ke Huang ◽  
Teng Su ◽  
...  

The progression in the hair follicle cycle from the telogen to the anagen phase is the key to regulating hair regrowth. Dermal papilla (DP) cells support hair growth and regulate the hair cycle. However, they gradually lose key inductive properties upon culture. DP cells can partially restore their capacity to promote hair regrowth after being subjected to spheroid culture. In this study, results revealed that DP spheroids are effective at inducing the progression of the hair follicle cycle from telogen to anagen compared with just DP cell or minoxidil treatment. Because of the importance of paracrine signaling in this process, secretome and exosomes were isolated from DP cell culture, and their therapeutic efficacies were investigated. We demonstrated that miR-218-5p was notably up-regulated in DP spheroid–derived exosomes. Western blot and immunofluorescence imaging were used to demonstrate that DP spheroid–derived exosomes up-regulated β-catenin, promoting the development of hair follicles.


Development ◽  
1964 ◽  
Vol 12 (3) ◽  
pp. 425-438
Author(s):  
F. J. Ebling ◽  
G. R. Hervey

Hair growth in the rat occurs in a series of waves, which start ventrally and pass over the flanks to the back (Dry, 1926; Butcher, 1934; Johnson, 1958a). The activity of the hair follicle is cyclic; when the hair has been fully formed there is a period of quiescence during which the dead hair is retained as a ‘club’. The duration of the complete cycle varies with site and age, ranging from 24 to about 100 days (Ebling & Johnson, 1964). When hair follicles are translocated, they continue to maintain the periodicity characteristic of their sites of origin (Ebling & Johnson, 1959). On the other hand, when skin is exchanged between rats of different ages and thus with their hair growth waves out of phase, follicular activity in the graft skin in some circumstances comes into line with the activity of the host (Ebling & Johnson, 1961).


Nutrients ◽  
2021 ◽  
Vol 13 (6) ◽  
pp. 2087
Author(s):  
Mizuki Ogawa ◽  
Miyako Udono ◽  
Kiichiro Teruya ◽  
Norihisa Uehara ◽  
Yoshinori Katakura

Enhanced telomerase reverse transcriptase (TERT) levels in dermal keratinocytes can serve as a novel target for hair growth promotion. Previously, we identified fisetin using a system for screening food components that can activate the TERT promoter in HaCaT cells (keratinocytes). In the present study, we aimed to clarify the molecular basis of fisetin-induced hair growth promotion in mice. To this end, the dorsal skin of mice was treated with fisetin, and hair growth was evaluated 12 days after treatment. Histochemical analyses of fisetin-treated skin samples and HaCaT cells were performed to observe the effects of fisetin. The results showed that fisetin activated HaCaT cells by regulating the expression of various genes related to epidermogenesis, cell proliferation, hair follicle regulation, and hair cycle regulation. In addition, fisetin induced the secretion of exosomes from HaCaT cells, which activated β-catenin and mitochondria in hair follicle stem cells (HFSCs) and induced their proliferation. Moreover, these results revealed the existence of exosomes as the molecular basis of keratinocyte-HFSC interaction and showed that fisetin, along with its effects on keratinocytes, caused exosome secretion, thereby activating HFSCs. This is the first study to show that keratinocyte-derived exosomes can activate HFSCs and consequently induce hair growth.


Development ◽  
1961 ◽  
Vol 9 (2) ◽  
pp. 285-293
Author(s):  
F. J. Ebiling ◽  
Elizabeth Johnson

Activity of the hair follicle is cyclic, periods of hair-growth alternating with periods of quiescence during which the dead hair is retained as a ‘club’. In the rat, hair-growth occurs in a series of waves which start ventrally and pass over the flanks to the back (Dry, 1926; Butcher, 1934; Johnson, 1958a). The object of our work was to find out how far such activity is dependent upon factors within the follicle and how far it is subject to systemic control. When hair follicles are translocated, either by rotation of grafts in the mid-flank or by transposition of flaps in two stages, they continue to maintain the periodicity characteristic of their sites of origin (Ebling & Johnson, 1959). Vascularization of such follicles is always consequent upon follicular activity, even when this is out of phase with the normal waves of hair-growth on the adjacent body.


Development ◽  
1970 ◽  
Vol 23 (1) ◽  
pp. 219-236
Author(s):  
R. F. Oliver

Hair follicles are essentially composed of two tissues. The inner epidermal component, which gives rise to, among other products, the keratinized hair shaft, is confluent with the surface epidermis and is ensheathed by the dermal component which is confluent with the pars papillaris of the dermis. A specialization of the dermal component is the dermal papilla which, in follicles producing hair, is enclosed by the epidermal matrix of the hair bulb and is connected to the dermal sheath by the papilla stalk. Many authorities have considered that the dermal papilla is an essential component of the hair follicle (reviews: Cohen, 1965; Oliver, 1969). It has been suggested that the dermal papilla may be involved in both the induction of follicle lengthening and hair growth during the proanagen phase (Chase, 1965) of the hair cycle, a concept now justified by direct experimentation in the vibrissa follicle at least (Oliver, 1967b), and perhaps also in determining the nature of the hair produced by a follicle.


Author(s):  
Megan A. Palmer ◽  
Eleanor Smart ◽  
Iain S. Haslam

AbstractCholesterol has long been suspected of influencing hair biology, with dysregulated homeostasis implicated in several disorders of hair growth and cycling. Cholesterol transport proteins play a vital role in the control of cellular cholesterol levels and compartmentalisation. This research aimed to determine the cellular localisation, transport capability and regulatory control of cholesterol transport proteins across the hair cycle. Immunofluorescence microscopy in human hair follicle sections revealed differential expression of ATP-binding cassette (ABC) transporters across the hair cycle. Cholesterol transporter expression (ABCA1, ABCG1, ABCA5 and SCARB1) reduced as hair follicles transitioned from growth to regression. Staining for free cholesterol (filipin) revealed prominent cholesterol striations within the basement membrane of the hair bulb. Liver X receptor agonism demonstrated active regulation of ABCA1 and ABCG1, but not ABCA5 or SCARB1 in human hair follicles and primary keratinocytes. These results demonstrate the capacity of human hair follicles for cholesterol transport and trafficking. Future studies examining the role of cholesterol transport across the hair cycle may shed light on the role of lipid homeostasis in human hair disorders.


Sign in / Sign up

Export Citation Format

Share Document