Expression of bone morphogenetic protein-7 in human scalp skin and hair follicles.
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Bone Morphogenetic Protein 7↗
Biomedical subjects
M A Adly
Publications and source records attributed to M A Adly.
Age-associated decrease of CD1d protein production in normal human skin.
BACKGROUND: CD1d belongs to a family of antigen-presenting molecules structurally related to the classical major histocompatibility complex class I proteins. OBJECTIVES: To examine the expression pattern of CD1d protein in normal human skin with ageing. METHODS: Twenty normal human skin biopsy specimens were obtained from 20 healthy individuals. The latter were divided into three age groups: children (5-20 years), adults (21-50 years) and the elderly (51-81 years). The intensity of CD1d protein production was examined in human skin using immunofluorescent and immunoalkalinephosphatase staining methods. RESULTS: In the epidermis, CD1d protein production was strong in the skin of the children and declined gradually with age, being moderate in adults and weak in the elderly. As compared with values in children, there was a statistically significant decrease (P<0.05) in CD1d protein production in the elderly. In the dermis, CD1d protein production was strong in the fibroblasts, sweat glands, sebaceous glands, blood vessels and hair follicles regardless of age. CONCLUSIONS: Our study reports a decreased CD1d protein production in normal human skin with ageing. The clinical ramifications of these observations mandate further investigations.
Adolescent↗
Human scalp skin and hair follicles express neurotrophin-3 and its high-affinity receptor tyrosine kinase C, and show hair cycle-dependent alterations in expression.
BACKGROUND: Neurotrophin (NT)-3 and its high-affinity receptor tyrosine kinase C (Trk C) are essential for nervous system development. These members of the NT family are also involved in murine hair morphogenesis and cycling. However, their role in human hair follicle (HF) biology remains to be elucidated. OBJECTIVES: To explore the role of NTs in human skin and HF biology. METHODS: The immunoreactivity (IR) of NT-3 and Trk C was studied in human scalp skin and HFs by immunofluorescent and light microscopic immunohistology. Skin biopsies were obtained from normal human scalp containing mainly anagen VI HFs from women (age 53-57 years) undergoing elective plastic surgery. RESULTS: Both NT-3 and Trk C showed prominent, yet distinct, IR patterns in human scalp anagen HFs (anagen VI), whereas they were weakly expressed in catagen and increased again in telogen HFs. Within HF compartments, NT-3 IR was prominent in the outer root sheath, inner root sheath, dermal papilla and connective tissue sheath. Trk C IR was prominent in all HF epithelial and mesenchymal compartments. Outside the HF, both NT-3 and Trk C showed prominent IR in the epidermis, sebaceous glands and sweat glands. CONCLUSIONS: These observations provide the first indication that NT-3 and Trk C are expressed in human scalp skin and HFs, and suggest that Trk C-mediated signalling is involved not only in murine but also in human HF biology. They may be useful in determining therapeutic strategies for the treatment of hair cycle and skin-related disorders.
Epithelial Cells↗
Expression of CD1d in human scalp skin and hair follicles: hair cycle related alterations.
BACKGROUND: CD1d belongs to a family of antigen presenting molecules that are structurally and distantly related to the classic major histocompatibility complex class I (MHC I) proteins. However, unlike MHC I molecules, which bind protein antigens, CD1d binds to lipid and glycolipid antigens. CD1d is expressed by cells of lymphoid and myeloid origin, and by cells outside of the lymphoid and myeloid lineages, such as human keratinocytes of psoriatic skin. AIMS: To investigate whether CD1d is also expressed in sun exposed skin and in the immuno-privileged anagen hair follicle. MATERIALS/METHODS: CD1d immunoreactivity was studied in human scalp skin and hair follicles of healthy women in situ by immunofluorescent and light microscopic immunohistology. Skin biopsies were obtained from normal human scalp containing mainly anagen VI hair follicles from women (age, 53-57 years) undergoing elective plastic surgery. RESULTS: CD1d showed strong immunostaining in human scalp skin epidermis, pilosebaceous units, and eccrine glands. In the epidermis, CD1d was strongly expressed by basal and granular keratinocytes. In hair follicles, CD1d was expressed in the epithelial compartment and showed hair cycle related alterations, with an increase in the anagen and a reduction in the catagen and telogen phases. CONCLUSIONS: These results suggest that CD1d plays a role in human scalp skin immunology and protection against lipid antigen rich infectious microbes. They also raise the question of whether keratinocytes of the immuno-privileged anagen hair follicle can present lipid antigens to natural killer T cells. These data could help provide new strategies for the manipulation of hair related disorders.
Antigens, CD1↗
Synaptic ribbon dynamics in photoreceptors of mice.
The present study deals with structural plasticity of a special type of chemical synapse, the ribbon synapse. Near the presynaptic membrane ribbon synapses contain conspicuous electron-dense synaptic bodies which appear mainly as rod-like profiles under the transmission electron microscope. In addition, club-shaped and spherical profiles may be present, the function of which is unclear. To gain some insight into the significance of the latter structures we studied their presence in rod-type photoreceptor cells of BALB/c mice under different lighting conditions. Quantification revealed that the club-shaped and the spherical profiles showed a clear light/dark dependence. They were virtually absent at night and increased strikingly in number when the animals were exposed to light. When darkness was extended into the morning, the profiles remained low in number. As the rod cells diminish their neurotransmitter release during the light phase, the present findings are interpreted as signs of synapse inactivation.
Animals↗
Ultrastructural changes of photoreceptor synaptic ribbons in relation to time of day and illumination.
PURPOSE: Electron microscopic sections through rod and cone ribbon synapses reveal mainly rodlike synaptic ribbon profiles, but a few unusual spherical and club-shaped profiles also occur. To elucidate the meaning of the latter two forms, the authors have investigated these ribbon synapses at different times during the 24-hour cycle and under various lighting conditions. METHODS: The various types of ribbon profiles were counted, and their sizes were measured by means of transmission electron microscopy in retinas of male BALB/c mice exposed to 12 hours light (lights on at 6 AM) and 12 hours dark (LD 12:12), continuous light, or continuous darkness for 4 days. RESULTS: A 24-hour study of mice exposed to LD 12:12 showed that spherical and club-shaped profile numbers ranged from 0% to 29%, depending on the time of day. They reached a maximum at 3 hours after light onset, followed by a gradual decrease to approach zero at night and reappearing after light onset the next morning. After 4 days of continuous light, the spherical profiles were significantly decreased in number (examined at 9 AM). After continuous darkness, the spherical and club-shaped profiles were significantly reduced in number. Administration of 4 hours of light after 92 hours of continuous darkness restored the number of spherical and club-shaped profiles to normal values. The rodlike ribbon profiles were found to be longer in darkness than in light. In rod terminals containing spherical profiles, the rodlike ribbon profiles were shorter than in terminals without spherical profiles. CONCLUSIONS. The club-shaped and the spherical profiles were related to the turnover of the synaptic ribbons. Soon after light exposure in the morning, the synaptic ribbons formed distal swellings, giving rise to club-shaped profiles and a decrease in length. The swellings appeared to bud off, thus forming spherical synaptic bodies. This article discusses whether these changes are signs of degradation of spent ribbons, or whether they play a physiological role related to the inactivation of the ribbon synapses after light exposure.
Animals↗