scholarly journals Altered Hypoxia-Induced and Heat Shock Protein Immunostaining in Secondary Hair Follicles Associated with Changes in Altitude and Temperature in Tibetan Cashmere Goats

Animals ◽  
2021 ◽  
Vol 11 (10) ◽  
pp. 2798
Author(s):  
Yanyu He ◽  
Xiu Liu ◽  
Jie De ◽  
Saihong Kang ◽  
John S. Munday
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Structural Features ◽  
Hair Shaft ◽  
Hair Follicles ◽  
Gansu Province ◽  
Outer Root Sheath ◽  
Average Temperature ◽  
Root Sheath ◽  
Cashmere Goats

This experiment compared secondary hair follicles (SFs) in Tibetan cashmere goats from two different steppes that were at different altitudes and had different temperatures. Twenty-four 2-year-old goats were studied. Twelve goats were from Rikaze in Tibet which is at an altitude of above 5000 m with an average temperature of 0 °C. The other 12 studied goats were from Huan County of Gansu Province which is around 2000 m above sea level with an average temperature of 9.2 °C. The structural features of SFs were assessed using light microscopy and transmission electron microscopy. The presence of HIF-1a, HIF-2a, HIF-3a, HSP27, and HOXC13 proteins was studied using immunohistochemistry and immunofluorescence. Light and electron microscopy revealed that the SFs of the Tibetan cashmere goats that lived in the Rikaze Steppe were in the proanagen stage in May. However, the SFs of the goats from the lower warmer Huan County were in the anagen stage at the same time. Immunohistochemistry revealed intense immunostaining for HIF-1a protein in the inner root sheath (IRS) and hair shaft (HS); immunostaining against HIF-2a in the outer root sheath (ORS) and IRS; HIF-3a protein immunostaining in the ORS; HSP27 immunostaining in the ORS, IRS, and HS; and HOXC13 immunostaining in the ORS and HS. HIF-1a protein expression in the IRS and HS was higher than the expression in the ORS (p < 0.05) while the expression of HIF-2a protein was higher in the ORS and IRS than the HS (p < 0.05). The expression of HIF-3a protein was higher in the ORS than in the IRS (p < 0.05). Expression of HOXC13 protein was higher in the ORS than in the IRS and HS (p < 0.05). Immunostaining of HIF-1a, HIF-2a, and HSP27 protein was significantly higher in SFs from cashmere goats from Rikaze than in goats from Huan (p < 0.05). In contrast, HOX13 protein immunostaining was significantly higher in cashmere goats from Huan than from Rikaze (p < 0.05). Significant differences were observed in the SFs of cashmere goats from two locations that differ in altitude and temperature. This suggests the differences in the secondary hair follicles could be due to the hypoxia and lower temperatures experienced by the goats in Rikaze. These results are useful in understanding how altitude and temperature influence SF development. Hair produced by the SFs are used for down fiber. Therefore, understanding of the factors that influence SF development will allow the production and harvest of these valuable fibers to be maximized.

scholarly journals Integrin-linked kinase is required for epidermal and hair follicle morphogenesis

2007 ◽  
Vol 177 (3) ◽  
pp. 501-513 ◽  
Author(s):  
Katrin Lorenz ◽  
Carsten Grashoff ◽  
Robert Torka ◽  
Takao Sakai ◽  
Lutz Langbein ◽  
...  
Keyword(s):  
Hair Follicle ◽  
Leading Edge ◽  
Hair Shaft ◽  
Hair Follicles ◽  
Membrane Dynamics ◽  
Epidermal Keratinocytes ◽  
Outer Root Sheath ◽  
Root Sheath ◽  
Integrin Linked Kinase

Integrin-linked kinase (ILK) links integrins to the actin cytoskeleton and is believed to phosphorylate several target proteins. We report that a keratinocyte-restricted deletion of the ILK gene leads to epidermal defects and hair loss. ILK-deficient epidermal keratinocytes exhibited a pronounced integrin-mediated adhesion defect leading to epidermal detachment and blister formation, disruption of the epidermal–dermal basement membrane, and the translocation of proliferating, integrin-expressing keratinocytes to suprabasal epidermal cell layers. The mutant hair follicles were capable of producing hair shaft and inner root sheath cells and contained stem cells and generated proliferating progenitor cells, which were impaired in their downward migration and hence accumulated in the outer root sheath and failed to replenish the hair matrix. In vitro studies with primary ILK-deficient keratinocytes attributed the migration defect to a reduced migration velocity and an impaired stabilization of the leading-edge lamellipodia, which compromised directional and persistent migration. We conclude that ILK plays important roles for epidermis and hair follicle morphogenesis by modulating integrin-mediated adhesion, actin reorganization, and plasma membrane dynamics in keratinocytes.

scholarly journals Characterization of Melanocytes in Wool-bearing Skin of Merino Sheep

1985 ◽  
Vol 38 (3) ◽  
pp. 245 ◽  
Author(s):  
JW Forrest ◽  
MR Fleet ◽  
GE Rogers
Keyword(s):  
Electron Microscopy ◽  
Copper Deficiency ◽  
Light And Electron Microscopy ◽  
Outer Root Sheath ◽  
Merino Sheep ◽  
Root Sheath ◽  
Experimentally Induced

The distribution and character of melanocytes in the wool-bearing skin of Merino sheep of known genotypes were examined by light and electron microscopy. In black Merino sheep (ww, homozygous recessive), melanocytes were localized within three regions of the skin: epidermal-dermal border, outer root sheath and follicle bulb. Melanocytes within these regions were found to be actively producing melanin, had numerous dendritic extensions and were able to transfer melanin to adjacent keratinocytes. In a black Merino sheep whose fibres were white due to an experimentally induced copper deficiency the melanocytes were amelanotic. In contrast, for both WW (homozygous dominant) and Ww (heterozygous) white Merino sheep melanocytes were observed only at the epidermal-dermal border of the epidermis. The melanocytes appeared also to differ in character containing less melanin, appearing less dendritic in shape and having a reduced ability to transfer melanin to adjacent keratinocytes. The gene for white fleece (W), therefore, appears able to regulate pigmentation in Merino sheep, at least in part, by controlling the location and activity of melanocytes within the wool-bearing skin.

Effect of Minoxidil Sulfate on the Growth of Human Anagen Hair Follicles Grown in Collagen Gels, and on the Colony Growth of Human Cultured Outer Root Sheath Cells in vitro.

1992 ◽  
Vol 54 (4) ◽  
pp. 727-732 ◽  
Author(s):  
Naoyuki UCHIDA ◽  
Takesi FUJIE ◽  
Seiji ARASE ◽  
Yosiroh NINOMIYA ◽  
Hideki NAKANISI ◽  
...  
Keyword(s):  
Colony Growth ◽  
Hair Follicles ◽  
Collagen Gels ◽  
Outer Root Sheath ◽  
Root Sheath ◽  
Anagen Hair ◽  
Outer Root Sheath Cells ◽  
Sheath Cells

scholarly journals Requirement of zinc transporter ZIP10 for epidermal development: Implication of the ZIP10–p63 axis in epithelial homeostasis

2017 ◽  
Vol 114 (46) ◽  
pp. 12243-12248 ◽  
Author(s):  
Bum-Ho Bin ◽  
Jinhyuk Bhin ◽  
Mikiro Takaishi ◽  
Koh-ei Toyoshima ◽  
Saeko Kawamata ◽  
...  
Keyword(s):  
Progenitor Cell ◽  
Hair Follicles ◽  
Zinc Transporter ◽  
Outer Root Sheath ◽  
Epithelial Homeostasis ◽  
Cell Proliferation And Differentiation ◽  
Root Sheath ◽  
Signaling Axis ◽  
Progenitor Cell Proliferation ◽  
Epidermal Development

Skin tissues, in particular the epidermis, are severely affected by zinc deficiency. However, the zinc-mediated mechanisms that maintain the cells that form the epidermis have not been established. Here, we report that the zinc transporter ZIP10 is highly expressed in the outer root sheath of hair follicles and plays critical roles in epidermal development. We found that ZIP10 marked epidermal progenitor cell subsets and that ablating Zip10 caused significant epidermal hypoplasia accompanied by down-regulation of the transactivation of p63, a master regulator of epidermal progenitor cell proliferation and differentiation. Both ZIP10 and p63 are significantly increased during epidermal development, in which ZIP10-mediated zinc influx promotes p63 transactivation. Collectively, these results indicate that ZIP10 plays important roles in epidermal development via, at least in part, the ZIP10–zinc–p63 signaling axis, thereby highlighting the physiological significance of zinc regulation in the maintenance of skin epidermis.

Sulfated hyaluronan‐containing artificial extracellular matrices promote proliferation of keratinocytes and melanotic phenotype of melanocytes from the outer root sheath of hair follicles

2019 ◽  
Author(s):  
Marie Schneider ◽  
Sandra Rother ◽  
Stephanie Möller ◽  
Matthias Schnabelrauch ◽  
Dieter Scharnweber ◽  
...  
Keyword(s):  
Hair Follicles ◽  
Extracellular Matrices ◽  
Outer Root Sheath ◽  
Root Sheath

scholarly journals Inhibition of Rab27a and Rab27b Has Opposite Effects on the Regulation of Hair Cycle and Hair Growth

2020 ◽  
Vol 21 (16) ◽  
pp. 5672
Author(s):  
Kyung-Eun Ku ◽  
Nahyun Choi ◽  
Jong-Hyuk Sung
Keyword(s):  
Hair Growth ◽  
Expression Patterns ◽  
Dermal Papilla ◽  
Hair Follicles ◽  
Hair Cycle ◽  
Outer Root Sheath ◽  
Dermal Papilla Cells ◽  
Root Sheath ◽  
Culture Models

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.

Structural features of forming and developing blood capillaries of the enamel organ of rat molar tooth germs observed by light and electron microscopy

2005 ◽  
Vol 265 (3) ◽  
pp. 335-342 ◽  
Author(s):  
E. Manzke ◽  
E. Katchburian ◽  
F.P. Faria ◽  
E. Freymüller
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Structural Features ◽  
Molar Tooth ◽  
Enamel Organ ◽  
Blood Capillaries ◽  
Tooth Germs ◽  
Rat Molar

Correlated 3D Light and Electron Microscopy of Large, Complex Structures: Analysis of Transverse Tubules in Heart Failure

1998 ◽  
Vol 4 (S2) ◽  
pp. 440-441
Author(s):  
Maryann E. Martone ◽  
Andrea Thor ◽  
Stephen J. Young ◽  
Mark H. Ellisman.
Keyword(s):  
Electron Microscopy ◽  
Electron Tomography ◽  
Light And Electron Microscopy ◽  
Structural Features ◽  
Electron Microscopic Level ◽  
Specimen Preparation ◽  
Large Sample Size ◽  
Electron Microscopic ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron

Light microscopic imaging has experienced a renaissance in the past decade or so, as new techniques for high resolution 3D light microscopy have become readily available. Light microscopic (LM) analysis of cellular details is desirable in many cases because of the flexibility of staining protocols, the ease of specimen preparation and the relatively large sample size that can be obtained compared to electron microscopic (EM) analysis. Despite these advantages, many light microscopic investigations require additional analysis at the electron microscopic level to resolve fine structural features.High voltage electron microscopy allows the use of relatively thick sections compared to conventional EM and provides the basis for excellent new methods to bridge the gap between microanatomical details revealed by LM and EM methods. When combined with electron tomography, investigators can derive accurate 3D data from these thicker specimens. Through the use of correlated light and electron microscopy, 3D reconstructions of large cellular or subcellular structures can be obtained with the confocal microscope,

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