Development of horns in merino sheep

1973 ◽  
Vol 21 (2) ◽  
pp. 153 ◽  
Author(s):  
AG Lyne ◽  
DE Hollis

Development of horns has been studied in 20 foetuses ranging in age from 55 to 144 days of gestation, and in 16 lambs, ranging in age from birth to 42 days. Samples from one adult have also been examined. An increase in the thickness of the epidermis appears to be the first indication of horn development, recognizable in a 75-day-old male foetus and in an 84-day-old female foetus. Primary hair follicles develop in the horn region and produce emerging hairs, but these follicles later degenerate and disappear. The sweat glands and sebaceous glands formed in association with these follicles also degenerate, usually after hair growth has ceased. Fusion of primary follicles is a common feature in the horn growing skin, particularly before hair formation; a common connective tissue sheath surrounds the lower parts of these fused follicles. No secondary follicles are formed in the horn region but some branching of the primary follicles has been observed. By 118 days of gestation the epidermis in the horn region becomes greatly thickened, with very long dermal papillae which are well vascularized and innervated. Medulla-like columns of cells are formed above each dermal papilla and these cells keratinize later than the cells between the columns. These medullary cells remain in contact with each other longer than do the other cells of the horny sheath. Numerous arteriovenous anastomoses, which develop at two levels in the dermis of the horn region, are in continuity with capillaries which enter the dermal papillae of the epidermis. An outgrowth of bone from the frontal region of the skull, which later becomes the bony core of the horn, is first seen in a male foetus at 118 days. Acetylcholinesterase-positive branched cells (Langerhans cells), present in the lower part of the thick epidermis of developing horns, are not discernible in fully formed horns.

1992 ◽  
Vol 133 (3) ◽  
pp. 467-NP ◽  
Author(s):  
R. Choudhry ◽  
M. B. Hodgins ◽  
T. H. Van der Kwast ◽  
A. O. Brinkmann ◽  
W. J. A. Boersma

ABSTRACT A mouse monoclonal antibody against the N-terminal region of human androgen receptor (AR) was used to identify receptors by immunoperoxidase staining in frozen serial sections of skin from scalp, face, limb and genitalia of men and women aged 30–80 years. AR staining was restricted to cell nuclei. In sebaceous glands, AR were identified in basal and differentiating sebocytes. The percentage of receptor-positive basal sebocyte nuclei in the temple/forehead region was greater in males (65%) than in females (29%). AR staining was restricted to the cells of dermal papillae in anagen and telogen hair follicles. The percentage of dermal papillae containing AR was greater in males (58%) than in females (20%). The number of positively stained dermal papillae was lowest in female scalp skin. In 163 hair follicles sectioned, AR were absent from germinative matrix, outer root sheath (including the bulge region), inner root sheath, hair shaft and hair bulb, and from the capillaries present in some large dermal papillae. AR were present in pilosebaceous duct keratinocytes, suggesting that androgens may influence pilosebaceous duct keratinization. AR were also identified in interfollicular epidermal keratinocytes and dermal fibroblasts although, in both cell types, intensity and frequency of staining were greatest in genital skin. AR were identified in luminal epithelial cells of apocrine glands in genital skin and in certain cells of the secretory coils of eccrine sweat glands in all body sites. This study indicates that androgens regulate sebaceous gland and hair growth by acting upon two different types of target cells, the epithelial sebocytes of sebaceous glands and the mesenchymal cells of the hair follicle dermal papilla. AR staining in either cell type was not influenced by age in adults. The distribution of AR in human skin is consistent with the diverse effects of androgens on the structure and function of skin and its appendages. Journal of Endocrinology (1992) 133, 467–475


2021 ◽  
Vol 5 (3) ◽  
pp. 573-579
Author(s):  
Inda Astri Aryani ◽  
Cayadi Sidarta Antonius ◽  
Suroso Adi Nugroho ◽  
Nopriyati

The pilosebaceous unit is a sebaceous gland with hair follicles. One of the hormones that affects the pilosebaceous unit is androgen, a steroid hormone that plays an important role in the expression of the phenotype of men and women. Androgen consist of testosterone and dihydrotestosterone which are activated by androgen receptors. Androgen in the pilosebaceous unit affect sebum production and hair growth. Androgen receptors in the sebaceous glands are found on sebocytes and in hair follicles in the dermal papillae of hair follicles


Author(s):  
Zekeriya Özüdoğru ◽  
Ramazan İlgün ◽  
Derviş Özdemir

In the study, it was aimed to reveal the morphological, morphometric and histological characteristics of sinus interdigitalis found in the fore and hind feet of Konya merino sheep. For this purpose, the fore and hind feet of 10 Konya merino sheep, weighing between 44-79 kg, were used. Sinus interdigitalis were dissected out from the feet, and after morphometric measurements were made, morphological examinations were performed and photographed. The shape of the sinus interdigitalis, present in all the forefeet and hind feet, resembled a pipe consisting of neck and body. It was determined that the neck part was longer than the body at all feet. The inner surface of the gland was covered with hair, and there was more hair on the neck than on the body. The weight of the gland, body length and diameter, flexura, canal length and diameter were measured morphometrically. In the measurements made, it was determined that all the values of the forefeet were higher than the hind feet. In histological examination, it was found that the wall of the sinus interdigitalis consists of three layers: epidermis, dermis and fibrous capsule, and in the dermis, hair follicles, sebaceous glands, m. arrector pili and sweat glands were found.


2021 ◽  
Vol 5 (6) ◽  
pp. 545-551
Author(s):  
Inda Astri Aryani ◽  
Cayadi Sidarta Antonius ◽  
Suroso Adi Nugroho ◽  
Nopriyati

The pilosebaceous unit is a sebaceous gland with hair follicles. One of the hormones that affects the pilosebaceous unit is androgen, a steroid hormone that plays an important role in the expression of the phenotype of men and women. Androgen consist of testosterone and dihydrotestosterone which are activated by androgen receptors. Androgen in the pilosebaceous unit affect sebum production and hair growth. Androgen receptors in the sebaceous glands are found on sebocytes and in hair follicles in the dermal papillae of hair follicles


1955 ◽  
Vol 46 (1) ◽  
pp. 19-30 ◽  
Author(s):  
E. S. E. Hafez ◽  
A. L. Badreldin ◽  
M. M. Shafei

The structure, distribution and dimensions of skin strata and sweat glands have been investigated in Egyptian buffaloes and cattle. Samples from sixteen body regions were taken from three adult bulls of both species. Identical studies were also made on one buffalo calf and two buffalo embryos. Serial vertical and horizontal sections were cut from each body region using the ‘terpineol paraffin wax’ method. The following results were obtained.1. Buffalo skin is characterized by dermal papillae enclosing papillomatous epidermis. The fibrous structure of the dermis is similar in both species. In buffaloes, the average thickness of skin, main epidermis, papillomatous epidermis, and cornium is 6·5 mm., 50, 115, and 11μ respectively. The epidermis coefficient is 12 for the main epidermis and 18 for the papillomatous epidermis. In cattle, the average thickness of skin, epidermis and cornium layer is 4·3 mm., 51 and 5 μ respectively, while the epidermis coefficient is 8.2. The average number of hair follicles per sq.cm. of skin is 394 in the buffalo and 2633 in cattle. Each hair follicle is accompanied by two large lobulated sebaceous glands in the buffalo, and one small bilobed gland in cattle.3. There is no species difference in the histology of the sweat glands. Each hair follicle is accompanied by one sweat gland in both species. In the buffalo, the body of the sweat gland is oval and convoluted, while the duct is twisted at its attachment to the body. In cattle, the body of the gland is elongated while the duct is straight. The number of sweat glands per sq.cm. of skin is 394 in the buffalo and 2633 in cattle. The dimensions of the sweat glands are larger in buffaloes than in cattle. The length, circumference and sweating surface of the gland is 0·58, 0·47, and 0·276 sq.mm. in the buffalo, and 0·47, 0·26, and 0·124 sq.mm. in cattle respectively. The glandular surface of sweat glands per sq.cm. of skin is 1·07 sq.cm. in the buffalo and 3·08 sq.cm. in cattle.4. The type of sweat gland secretion is apocrine in both species. In the buffalo, successive stages of apocrine secretion are observed, and the merocrinelike form is rare. In cattle, the merocrine-like form prevails and the other stages are very rare. The theory (Findlay & Yang, 1950) of intraluminal transformation, of secretory products from coarse granularity to fluid homogeneity is supported. The effect of locality on the type of sweating activity is stressed.5. There are species differences in the distribution of blood vessels and capillaries. In the subepidermal level, the arterial branches are more frequent and superficial in buffaloes than in cattle. Capillaries are found in the dermal papillae of buffalo skin. The capillary loops encircling the hair follicle are more frequent in cattle than in buffaloes. The blood capillaries supplying the sebaceous glands are more numerous in the buffalo than in cattle. The blood supply of sweat glands is poor in both species.6. There are age differences in the skin histology. The number of hair follicles per sq.cm. of skin in a 5-months-old embryo, calf at birth, and adult buffaloes is 10560, 1248 and 400 respectively. There are no skin glands in the 1-month and 5-months-old embryos. The sweat gland in the calf is small in size and similar in structure to that of the adult. Calves have fewer sweat glands than adults.7. The body conformation and the degree of pigmentation are affected by species, breed and locality.8. The secreting activity of the sweat glands may be affected by the locality.9. It seems that there are species differences in the mechanism of heat convection and radiation, insensible perspiration and sensible perspiration, due to histological differences.


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.


1993 ◽  
Vol 101 (s1) ◽  
pp. 114S-120S ◽  
Author(s):  
Valerie Anne Randall ◽  
Margaret Julie Thornton ◽  
Andrew Guy Messenger ◽  
Nigel Andrew Hibberts ◽  
Andrew Stewart Irving Loudon ◽  
...  

Development ◽  
1992 ◽  
Vol 116 (3) ◽  
pp. 563-571 ◽  
Author(s):  
K.A. Horne ◽  
C.A. Jahoda

The capacity of lower follicle dermal sheath to restore hair growth was tested by removing the lower halves of follicles, and then immediately implanting material containing dermal sheath cells from these bases, into the remaining upper epidermal follicle cavity. Over 60% of recipient follicles produced stout emergent vibrissa fibres and some operations resulted in multiple hair production from a single follicle. Histological examination revealed new dermal papillae within large bulb structures which were sited below the level of amputation--a feature that indicated that the new dermal papilla was derived from implanted material. For many follicles, the failure to produce emergent fibres could be accounted for after histological examination. These results provide clear evidence that lower follicle dermal sheath cells are capable of replacing those of the dermal papilla and it shows that they can do so in the context of the upper follicle. However, because elements of lower follicle epidermis were present in the implant material, the interactive sequence of events cannot be established. Dermal sheath cells have immense potential for papilla cell replacement: questions remain as to whether the distinction between sheath and papilla cells is one of context, or whether the transition requires specific external influences.


2020 ◽  
Vol 21 (16) ◽  
pp. 5672
Author(s):  
Kyung-Eun Ku ◽  
Nahyun Choi ◽  
Jong-Hyuk Sung

Rab27a/b are known to play an important role in the transport of melanosomes, with their knockout causing silvery gray hair. However, the relationship between Rab27a/b and hair growth is not well known. To evaluate the role of Rab27a/b in hair cycle, we investigated the expression of Rab27a/b during hair cycling and human outer root sheath (hORS) cells. The expression of Rab27a in ORS cells was mainly detected at the anagen, whereas expression of Rab27b in ORS, and epidermal cells was strongly expressed at the telogen. Additionally, Rab27a/b were expressed in the Golgi of hORS cells. To evaluate the role of Rab27a/b in hair growth, telogen-to-anagen transition animal and vibrissae hair follicles (HFs) organ culture models were assayed using Rab27a/b siRNAs. The knockdown of Rab27a or Rab27b suppressed or promoted hair growth, respectively. These results were also confirmed in human dermal papilla cells (hDPCs) and hORS cells, showing the opposite mitogenic effects. Moreover, Rab27b knockdown increased the expression levels of various growth factors in the hDPCs and hORS cells. Overall, the opposite temporal expression patterns during hair cycling and roles for hair growth of Rab27a/b suggested that Rab27a/b might regulate the hair cycle. Therefore, our study may provide a novel solution for the development of hair loss treatment by regulating Rab27a/b levels.


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.


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