Introduction
Hair is a component of the integumentary system and extends downward into the dermal layer, where it sits in the hair follicle. Humans haveapproximately five million hair follicles, which offer protection from cold and UV radiation, produce sebum, and can have a significant psychological impact when growth or structure is unbalanced.[1]
At a microscopic level, each hair's variety in length, color, diameter, and cross-sectional shape creates the characteristic profiles seen across ethnic groups and among individuals. This activity will discuss the physiology of hair, cellular components, mechanisms of growth and differentiation, and its clinical significance.[1]
Cellular Level
Each strand of hair is made up of two separate structures.The first is the hair shaft, which comprises the visible part outside the skin, and the second is the hairfollicle, which lies underneath the skin's surface.Additionally, the hair follicle contains an inner and outer root sheath.
Hair comprises living and non-living components above and below the epidermis level. Above the epidermis, the hair shaft is a thin, flexible cylinder of non-living, keratinized epithelial cells. Below the epidermis, it is part of a living hair follicle that enlarges at the base and forms the hair bulb.
The hair shaft comprises a cortex, surrounding cuticle cells, and sometimes a central medulla found in thicker hair. The bulk of this hair fiber belongs to the cortical layer, which plays a vital role in determining the physical and mechanical properties of the hair, such as strength, texture, and color.The shaft is composed predominantly of macrofibrils, which are rods of microfibrils meshed together in a matrix.
The follicle is the primary structure from which hair can grow. The histological arrangement of the follicle is divided into outer and inner root sheaths.
The outer root sheath (ORS) has been recognized as a ready supply of multipotent stem cells that differentiate into several cell types, including melanocytes and keratinocytes. More specifically, these stem cells are thought to reside in a distinct bulge area located between the insertion of the arrector pili muscle and the ductal opening of the sebaceous gland.
The inner root sheath (IRS) consists of the Henle layer, the Huxley layer, and the previously mentioned cuticle layer, which also helps affix the growing hair shaft to the follicle, a task bolstered by the production of keratins and trichohyalin by the IRS cells.The cuticlecomprises flat overlapping cells covering the hair shaft from the root until it exits from the epidermis. The cuticle is of considerable cosmetic importance as it gives the hair an untangled appearance and shape.
The hair bulb is the region of the follicle that actively produces hair.The bulb extends into the dermal layer of the skin and surrounds the dermal papilla, an important structure derived from mesenchyme, made of rich stroma, associated nerve fibers, and a loop of the capillary that supplies nutrients. The papilla is believed to be a primary orchestrator in the hair growth process, conducting the precise signals that determine the size and color of the hair shaft via a complex mix of essential growth factors, including insulin-like growth factor, stem cell factor, keratinocyte growth factor, and bone morphogenetic protein. The hair bulb itself is divided into two regions by the Auber line. Below this line, cells still undergo differentiation. The immature cells below the Auber line comprise the germination center or matrix of the follicle, where all cells are mitotically active and move upward where they enlarge, elongate vertically, and integrate into the hair shaft.[2]
Nerve supply to the hair follicles is similar to that of the surrounding network of dermal nerves in that it is composed of both sensory afferents and autonomic sympathetic nerves. Sensory information from hair stimulation enhances tactile ability. Autonomic nervous innervation primarily provides control of the arrector pili muscle. Contraction of these tiny muscles makes the hair "stand on end." This is likely a vestigial function related to fur; erecting the shafts served to trap air, conserve heat in cold climates, and cut a larger silhouette to intimidate rivals or would-be predators.
Vascular supply is provided by small arterioles originating in the subcutaneous fat. The vessels nourish the hair follicle by delivering oxygen and nutrients, eliminating waste, and promoting growth. Subtle hair loss on the lower extremities can sometimes hint at the underlying peripheral arterial disease.
Hair that is darker, thicker, andmore visibleto the human eye is called terminal hair. Areas of the body that appear to be hairless but have shorter, finer hairs that lack the medulla layer are called vellus hair. Neonates can be born with lanugo hair; finehairs shed in utero or within the first weeks of life.[3] Club hair is fully keratinized hair that is fully formed in the telogen stage of the hair cycle. The only parts of the external surface of the body that are truly hairless are the palms and soles of the hands and feet, lips, labia minora, and glans penis.
Development
Hair growth is regulated by vascular, endocrine, and neural stimuli in addition to age and nutritional habits. Hair from the scalp is shed at approximately 100to 200 follicles/day and grows ata rate of about 0.35 mm/day, 1 cm/month, or 15 cm/year.[4]
Atbirth, the body is covered with tiny, vellus hairs, except for the terminal hairs located on the scalp, eyelashes, and eyebrows. During puberty, androgens influence some vellus hairs, such as those of the face (beard), axilla, genital area, and trunk,and differentiate them into terminal hairs, which are longer, thicker, and pigmented.[5]
Function
The human body is covered almost entirely with hair, most of which are tiny, colorless vellus hairs. As mentioned above, the few places devoid of hair include the palms, soles, and mucosal regions of lips and external genitalia. Mammalian hair has many functions, including protection against external elements, thermoregulation, producing pheromones, apocrine sweat, and sebum, and playing a role in social interactions.[1]
Mechanism
Like skin, hair forms by rapid division and differentiation of stem cells, forming keratinocytes that migrate, flatten, and die, forming keratinized cells. The final hair product exposed on the skin's surface will be composed entirely of keratin. The growth of the hair follicle is cyclical. Stages of rapid growth and elongation of the hair shaft alternate with periods of quiescence and regression driven by apoptotic signals. This cycle can be divided into three phases: anagen (growth), catagen (transition), and telogen (rest).
Anagen growth is the active phase in which the hair follicle takes on its onion-like shape and works to produce the hair fiber. The anagen phase can be further broken down into proanagen and metanagen phases. Proanagen sees the follicle proliferating hair progenitor cells and begins the differentiation process. The new hair shaft appears on the skin's surface to mark the metanagen phase. The anagen phase as a whole can last for several years.
The catagen phase begins with the end of the anagen phase and is characterized by a transition into quiescence. During this phase, which can last a few weeks, the hair follicle undergoes apoptosis-driven regression and loses about one-sixth of its standard diameter. The formation of a club hair, an important prognostic indicator in assessing hair pathology, also occurs at this time. If many hairs form club hair at once and are subsequently shed, it can give the appearance of thinning. Some conditions this may occur in include, but are not limited to, hypothyroidism, hyperthyroidism, stress, vitamin deficiencies, and post-childbirth.
Next is the telogen or resting phase of the hair cycle, in which the hair follicle is dormant, and growth of the hair shaft does not occur. About 10to 15% of all hairs on the body are in this resting phase at any given time and can remain in this state for a variable amount of time, depending on the location of the hair - from a few weeks for eyelashes to nearly one year for scalp hair. The exact mechanism that controls passage from one phase into the next is not fully known.
The bulge activation theory posits that growth factors produced in the dermal papilla stimulate bulge stem cells to proliferate and modulate growth-phase transitions. Because these cells are transient amplifying cells, they can only go through a limited number of mitoses, thereby setting the duration of anagen and onset of catagen phases.[6]
The hair follicle and its product are also one of the few areas of the body protected from immune surveillance in a phenomenon first described by Sir Peter Medawar in 1948 as an immune privilege (IP). IP is achieved via severalmajor histocompatibility complexes by the follicle, local production of immune modulators such as TGF-beta, and expression of Fas-Ligand to kill autoreactive T cells.[7]
Clinical Significance
Hair has many areas of clinical significance, which include diseases of hair loss, excess, alterations due to nutritional deficiencies, infectious causes, and effects of drug reactions.
The unwanted loss of hair, known as alopecia, is a widespread condition affecting both sexes, occurring in numerous patterns, and classified into non-scarring and scarring (cicatricial) subtypes.
The most common non-scarring type of alopecia is androgenetic or “pattern” hair loss which develops due to a combination of genetic predisposition and the action of androgen on hair follicles. While men are more commonly associated with this condition, women can also be affected and exhibit their own characteristic loss pattern. The hair loss typically begins in both temples and recedes to form an “M” shape.[8]
This is not to be confused with traction alopecia,which is seen in people wearingtight braids and ponytails that place excessive force on the hairline resulting in hair breakage and hairline recession.[9]
Alopecia areata is patchy hair loss, usually on the scalp, which often has the characteristic “exclamation point” hairs that are short and broken and appear to be floating exclamation marks.Alopecia totalis and universalis are the most severe forms of alopecia. Alopecia totalis eradicates all terminal scalp hairs alopecia universalis eradicates all body hairs. Former NBA athlete Charlie Villanueva displays this pattern of alopecia.[10]
Scarring alopecia can arise from cutaneous manifestations of lupusor a bacterial inflammatory condition known as dissecting folliculitis. These alopecia patterns exhibit shiny, bare skin patches, resulting in permanent hair loss in the affected areas.[10]
Telogen effluvium is when hair roots are pushed into the telogen resting phase. This usually occurs after some stress and can be acute or chronic.
A proliferation of fine lanugo hairs past the neonatal period can be a symptom of malnutrition and aid in diagnosing anorexia nervosa. Hair loss can also be due to an infection, like tinea capitis, which is a fungal infection that results in a patch of hair loss on the scalp.[11] A kerion, a fungal abscess, can sometimes form and result in hair loss, most commonly on the scalp and sometimes on the face, torso, and extremities.Hair transplantation has become a therapeutic option for those who fail to have hair growth with medication.
Excess hair or hair in abnormal locations is known as hypertrichosis. Hypertrichosis can be seen in porphyria cutanea tarda, where people experience photosensitivity blistering and hypertrichosis.This condition can develop as an inherited condition or a drug reaction, for example,following the use of phenytoin, cyclosporine, and minoxidil.[12]
Trichotillomania is an impulse control disorder in which the affected individual cannot resist the urge to obsessively pull out or break their hair. These individuals may obsessively pull hair from anywhere on their body, including their scalp, eyebrows, and eyelashes.[13]
References
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Gupta AK, Friedlander SF, Simkovich AJ. Tinea capitis: An update. Pediatr Dermatol. 2022 Mar;39(2):167-172. [PubMed: 35075666]
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Rudnick S, Phillips J, Bonkovsky H., Porphyrias Consortium of the Rare Diseases Clinical Research Network. Familial Porphyria Cutanea Tarda. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. University of Washington, Seattle; Seattle (WA): Jun 6, 2013. [PubMed: 23741761]
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Huynh M, Gavino AC, Magid M. Trichotillomania. Semin Cutan Med Surg. 2013 Jun;32(2):88-94. [PubMed: 24049966]
Disclosure: Ezra Hoover declares no relevant financial relationships with ineligible companies.
Disclosure: Mandy Alhajj declares no relevant financial relationships with ineligible companies.
Disclosure: Jose Flores declares no relevant financial relationships with ineligible companies.
