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exogen in the hair follicle cycle

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Exogen in the hair follicle cycle

The study of hair follicle has gained importance due to its implicit relation to the study of major biological phenomena. Half a century ago Chase in his review defined the dynamics of hair growth and the cycling of the follicle. Today the biological and psychosocial importance of hair growth is realized even more. In humans, the hair shaft plays a major role in influencing social intercourse. Fortunately, with the availability of various analytical tools, the medical world today believes that with proper therapeutic intervention, hair growth can be controlled to a considerable extent.

It is important to understand a little of hair biology. The hair follicles differ according to their location in the body, but their main function is to grow a hair shaft, which has the same basic structure. The hair follicle grows from the embryonic epidermis. The central cylinder forms the shaft, the outer cylinder forms the outer root sheath and the middle cylinder is the inner root sheath. The shaft grows because of the rapidly multiplying matrix cells in the hair bulb. As these cells move upwards, they acquire shape by being compressed by the inner root sheath. The dermal papilla controls the number of matrix cells thus determining the size of the hair.

All mature hair follicles undergo a cyclical process consisting of four phases - anagen (growth), catagen (regression), telogen (rest) and exogen (shedding). This is a regenerative system and is continued over the lifetime of a mammal. Exogen is perhaps of most significance from a patient’s perspective, but medically very little attention has been given to it. The control mechanism for exogen is quite independent of catagen and telogen because it is not unusual for humans to retain the telogen hair for more than one follicular cycle.


Mechanism of exogen

As hair follicle cycling is an evolutionary process, each hair follicle has its own rhythm of anagen, catagen, telogen and exogen. On any given day, human beings lose about 50-150 scalp hairs due to exogen. About 5 to 15 percent of scalp-hairs are at the telogen stage at any given time. So shedding of this hair may be considered normal. Shedding in excess of this may be due to an increase in the follicles of scalp hair in the telogen stage and should be addressed to contain hair loss.

The how and why of hair follicle cycling remains largely unanswered and several theories have been propounded by biologists. The main focus of hair research remains to determine the molecular signals that trigger the change from one phase to the other. As protease seems to play an important role in the attachment of the hair club, people being treated with protease inhibitors for immunodeficiency virus suffer from excessive hair shedding. The exogen phase may also sometimes be altered in the case of certain diseases. A delayed exogen occurs in the case of trichostasis spinulosa where hair shaft from previous cycles are retained and the infundibulum of the hair follicle becomes dilated. In androgenetic alopecia, the hair shaft sheds before the onset of anagen so no shaft fills the pilary canal. The exogen process often starts earlier in such cases.

Although exogen deals with the shaft base and not directly with the hair follicle, exogen and anagen influence one another. The details of this mechanism may be yet unknown but the therapeutic management of one disorder is certainly dependent upon the control of the other process.

The controls of exogen may be understood a little by studying the environmental factors like light, temperature, and nutrition affecting molt in sheep. But there is also innate local control of exogen as suggested by the fact that each fiber grows to a specific length for a specific time before they are shed. This local control must involve genetics.

Little is known about how the resting hair shaft comes to the base of the telogen follicle or how it is attached there. As the catagen phase ends, the hair shaft moves upwards with a shortening of the inner root sheath. A trichilemmal keratinization starts and provides an adherent base to the lower keratinizing shaft. The telogen shaft base is anchored into this trichilemmal base of the upper outer root sheath. The cells surrounding the attachment site are rich in desmosomes and keratin.

Studies with transgenic mouse have shown an active role of DG3 and K14 in the mooring of the club hair. Mooring defect was also observed in case of mice with an inadequate lysosomal protease. Thus, though lack of DG3 may not indicate the process of exogen but it establishes the importance of a tight grip of the surrounding epithelial cells for mooring of hair. Recent studies have also shown, secretions of a chymotyptic enzyme by the sebaceous gland, and that a plasminogen activator inhibitor manifests in the cells of the attachment site. This has led to the conclusion that proteolytic pathways play a critical role in process of exogen on hair shedding.


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