scholarly journals Stiffness of Human Hair Correlates with the Fractions of Cortical Cell Types

Cosmetics ◽  
2019 ◽  
Vol 6 (2) ◽  
pp. 24 ◽  
Author(s):  
Yusuke Ezawa ◽  
Shinobu Nagase ◽  
Akira Mamada ◽  
Shigeto Inoue ◽  
Kenzo Koike ◽  
...  
Keyword(s):  
Human Hair ◽  
Fluorescent Dyes ◽  
Cortical Cell ◽  
Cell Types ◽  
Cortical Cells ◽  
Force Microscopy ◽  
Bending Modulus ◽  
Hair Samples ◽  
Fluorescence Light ◽  
The Difference

(1) Background: The objective of this work was to elucidate the hair microstructure which correlates with the stiffness of human hair fibers. (2) Methods: Bending moduli of hair fibers were evaluated for the hair samples from 156 Japanese female subjects. Hair transverse sections were dual-stained with fluorescent dyes which can stain para- and ortho-like cortical cells separately, and observed under a fluorescence light microscope. Atomic force microscopy nanoindentation measurements were performed to examine the modulus inside macrofibrils. (3) Results: The difference in bending moduli between the maximum and the minimum values was more than double. The hair of high bending modulus was rich in para-like cortical cells and the bending modulus significantly correlated with the fraction of para-like cortical cells to the whole cortex. On the other hand, the elastic moduli inside macrofibrils were almost same for the para- and ortho-like cortical cells. (4) Conclusions: Hair bending modulus depends on the fractions of the constitutional cortical cell types. The contribution of the intermacrofibrillar materials, which differed in their morphologies and amounts of para- and ortho-like cortical cells, is plausible as a cause of the difference in the modulus of the cortical cell types.

Cortical cell types and intermediate filament arrangements correlate with fiber curvature in Japanese human hair

2009 ◽  
Vol 166 (1) ◽  
pp. 46-58 ◽  
Author(s):  
Warren G. Bryson ◽  
Duane P. Harland ◽  
Jonathan P. Caldwell ◽  
James A. Vernon ◽  
Richard J. Walls ◽  
...  
Keyword(s):  
Intermediate Filament ◽  
Human Hair ◽  
Cortical Cell ◽  
Cell Types

scholarly journals Comprehensive in situ mapping of human cortical transcriptomic cell types

2021 ◽  
Vol 4 (1) ◽  
Author(s):  
Christoffer Mattsson Langseth ◽  
Daniel Gyllborg ◽  
Jeremy A. Miller ◽  
Jennie L. Close ◽  
Brian Long ◽  
...  
Keyword(s):  
Brain Function ◽  
Cortical Cell ◽  
Cell Types ◽  
Cell Type ◽  
Cortical Cells ◽  
Human Cortex ◽  
Single Nucleus ◽  
Genetic Signatures ◽  
Cell Typing

AbstractThe ability to spatially resolve the cellular architecture of human cortical cell types over informative areas is essential to understanding brain function. We combined in situ sequencing gene expression data and single-nucleus RNA-sequencing cell type definitions to spatially map cells in sections of the human cortex via probabilistic cell typing. We mapped and classified a total of 59,816 cells into all 75 previously defined subtypes to create a first spatial atlas of human cortical cells in their native position, their abundances and genetic signatures. We also examined the precise within- and across-layer distributions of all the cell types and provide a resource for the cell atlas community. The abundances and locations presented here could serve as a reference for further studies, that include human brain tissues and disease applications at the cell type level.

scholarly journals Comprehensive in situ mapping of human cortical transcriptomic cell types

2021 ◽  
Author(s):  
Christoffer Mattsson Langseth ◽  
Daniel Gyllborg ◽  
Jeremy A. Miller ◽  
Jennie L. Close ◽  
Brian Long ◽  
...  
Keyword(s):  
Brain Function ◽  
Cortical Cell ◽  
Cell Types ◽  
Expression Data ◽  
Cortical Cells ◽  
Human Cortex ◽  
Single Nucleus ◽  
Genetic Signatures ◽  
Cell Typing

The ability to spatially resolve the cellular architecture of human cortical cell types over informative areas is essential to understanding brain function. We combined in situ sequencing gene expression data and single-nucleus RNA-sequencing cell type definitions to spatially map cells in sections of the human cortex via probabilistic cell typing. We mapped and classified a total of 59,816 cells into all 75 previously defined subtypes to create a first spatial atlas of human cortical cells in their native position, their abundances and genetic signatures.

Synthesis of alpha 2-macroglobulin by bovine adrenal cortical cell cultures

1989 ◽  
Vol 256 (4) ◽  
pp. C779-C785 ◽  
Author(s):  
N. Kirshner ◽  
J. J. Corcoran ◽  
H. P. Erickson
Keyword(s):  
Cell Cultures ◽  
Culture Medium ◽  
Cultured Cells ◽  
Primary Cultures ◽  
Cortical Cell ◽  
Cell Types ◽  
Cortical Cells ◽  
Weight Protein ◽  
Cortical Cell Cultures ◽  
Adrenal Cortical Cells

Primary cultures of bovine adrenal medullary cells synthesize and secrete a high-molecular-weight protein into the culture medium. The protein was purified from the serum-free medium of cultured cells and was identified as alpha 2-macroglobulin by gel electrophoresis, sedimentation velocity, electron microscopy, immunoprecipitation, immunodiffusion, and autoradiography. Antisera directed against the protein were prepared and used to determine the cell types that synthesize the protein. Immunohistofluorescence studies show that adrenal cortical cells present in the adrenal medullary cell cultures reacted with the antisera to the protein purified from the medium, but adrenal medullary chromaffin cells did not. Cell cultures prepared from bovine adrenal cortex also synthesize and secrete alpha 2-macroglobulin and react with the antisera.

Human-hair analysis

1992 ◽  
Vol 50 (1) ◽  
pp. 886-887
Author(s):  
Brenda E. Lambert ◽  
Ernest C. Hammond
Keyword(s):  
Human Hair ◽  
Hair Analysis ◽  
Hair Shaft ◽  
White Female ◽  
Chemical Processing ◽  
X Ray ◽  
Hair Samples ◽  
Wave Technique ◽  
Permanent Wave ◽  
Scanning Electron

The purpose of this study was to examine the external structure of four human hair shaft samples with the scanning Electron Microscope (SEM) and to obtain information regarding the chemical composition of hair by using the attached x ray microanalysis unit.The hair samples were obtained from two female subjects. Sample A was taken from a black female and had not undergone any type of chemical processing. Sample B, C, D were taken from a white female, and were natural, processed, and unpigmented, i.e. “gray”, respectively. Sample C had been bleached, tinted, and chemically altered using a permanent wave technique.

Generalized Heterodyne Configurations for Photo-induced Force Microscopy

2019 ◽  
Author(s):  
Le Wang ◽  
Devon Jakob ◽  
Haomin Wang ◽  
Alexis Apostolos ◽  
Marcos M. Pires ◽  
...  
Keyword(s):  
Spatial Resolution ◽  
Repetition Rate ◽  
Modulation Frequency ◽  
High Harmonic ◽  
Chemical Imaging ◽  
Heterodyne Detection ◽  
Force Microscopy ◽  
Wide Range ◽  
The Difference ◽  
Afm Cantilever

<div>Infrared chemical microscopy through mechanical probing of light-matter interactions by atomic force microscopy (AFM) bypasses the diffraction limit. One increasingly popular technique is photo-induced force microscopy (PiFM), which utilizes the mechanical heterodyne signal detection between cantilever mechanical resonant oscillations and the photo induced force from light-matter interaction. So far, photo induced force microscopy has been operated in only one heterodyne configuration. In this article, we generalize heterodyne configurations of photoinduced force microscopy by introducing two new schemes: harmonic heterodyne detection and sequential heterodyne detection. In harmonic heterodyne detection, the laser repetition rate matches integer fractions of the difference between the two mechanical resonant modes of the AFM cantilever. The high harmonic of the beating from the photothermal expansion mixes with the AFM cantilever oscillation to provide PiFM signal. In sequential heterodyne detection, the combination of the repetition rate of laser pulses and polarization modulation frequency matches the difference between two AFM mechanical modes, leading to detectable PiFM signals. These two generalized heterodyne configurations for photo induced force microscopy deliver new avenues for chemical imaging and broadband spectroscopy at ~10 nm spatial resolution. They are suitable for a wide range of heterogeneous materials across various disciplines: from structured polymer film, polaritonic boron nitride materials, to isolated bacterial peptidoglycan cell walls. The generalized heterodyne configurations introduce flexibility for the implementation of PiFM and related tapping mode AFM-IR, and provide possibilities for additional modulation channel in PiFM for targeted signal extraction with nanoscale spatial resolution.</div>

Plant Oil-Based Nanoemulsions: Preparation and Efficacy for Hair Treatment

2020 ◽  
Vol 04 ◽  
Author(s):  
Lívia Gonçalves Ferreira Rodrigues ◽  
Juliana Falcão Alves de Carvalho ◽  
Cristal dos Santos Cerqueira Pinto ◽  
Elisabete Pereira Santos ◽  
Claudia Regina Elias Mansur
Keyword(s):  
Human Hair ◽  
Mechanical Tests ◽  
Plant Oils ◽  
Plant Oil ◽  
Oil In Water ◽  
Hair Samples ◽  
Poly Ethylene Oxide ◽  
Treatment Objective ◽  
Poly Ethylene ◽  
Average Size

Background:: The use of polymers in hair care products is widespread, and silicones in particular are extensively used in cosmetic formulations. In addition, plant oils can also be used for hair treatment. Objective: In the present work, oil-in-water (O/W) nanoemulsions were prepared to repair chemical damage to human hair samples, to investigate the combined use of a silicone polyether copolymer (surfactant) that has a branch composed of poly(ethylene oxide) in its chains, and two types of plant oils: coconut and ojon oil. Materials and Methods:: Surfactant-oil-water formulations were obtained by ultrasonic processing. The nanoemulsions were then applied to human hair strands previously damaged with sodium hydroxide, to compare the treated strands with untreated ones. The efficacy of the formulations was investigated by scanning electron microscopy, thermogravimetric analysis and mechanical tests. Results and Discussion:: Stables nanoemulsions were obtained with average size of the dispersed droplets up to 400 nm. The micrographs suggest that the action mechanism of the nanoemulsions depends not only on the type of plant oil used and size of the droplets dispersed in the system, but also on the type of hair that receives the treatment. The thermal analysis showed that the use of nanoemulsion changed the temperature of keratin interconversion to higher values, which can make hair fibers more resistant to heat. Hair resistance was improved when comparing virgin samples to the damaged ones. Conclusion:: The nanoemulsions were efficient in the treatment of the hair samples, which showed a significant improvement of their mechanical properties.

scholarly journals Determination of Vitamin B3 Vitamer (Nicotinamide) and Vitamin B6 Vitamers in Human Hair Using LC-MS/MS

Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4487
Author(s):  
Sundus M. Sallabi ◽  
Aishah Alhmoudi ◽  
Manal Alshekaili ◽  
Iltaf Shah
Keyword(s):  
Human Hair ◽  
Vitamin B6 ◽  
Low Density Lipoprotein ◽  
Density Lipoprotein ◽  
Reversed Phase ◽  
Water Soluble ◽  
Vitamin B3 ◽  
Hair Samples ◽  
Pyridoxal Hydrochloride ◽  
Vitamin B3 Deficiency

Water-soluble B vitamins participate in numerous crucial metabolic reactions and are critical for maintaining our health. Vitamin B deficiencies cause many different types of diseases, such as dementia, anaemia, cardiovascular disease, neural tube defects, Crohn’s disease, celiac disease, and HIV. Vitamin B3 deficiency is linked to pellagra and cancer, while niacin (or nicotinic acid) lowers low-density lipoprotein (LDL) and triglycerides in the blood and increases high-density lipoprotein (HDL). A highly sensitive and robust liquid chromatography–tandem mass spectroscopy (LC/MS-MS) method was developed to detect and quantify a vitamin B3 vitamer (nicotinamide) and vitamin B6 vitamers (pyridoxial 5′-phosphate (PLP), pyridoxal hydrochloride (PL), pyridoxamine dihydrochloride (PM), pridoxamine-5′-phosphate (PMP), and pyridoxine hydrochloride (PN)) in human hair samples of the UAE population. Forty students’ volunteers took part in the study and donated their hair samples. The analytes were extracted and then separated using a reversed-phase Poroshell EC-C18 column, eluted using two mobile phases, and quantified using LC/MS-MS system. The method was validated in human hair using parameters such as linearity, intra- and inter-day accuracy, and precision and recovery. The method was then used to detect vitamin B3 and B6 vitamers in the human hair samples. Of all the vitamin B3 and B6 vitamers tested, only nicotinamide was detected and quantified in human hair. Of the 40 samples analysed, 12 were in the range 100–200 pg/mg, 15 in the range 200–500 pg/mg, 9 in the range of 500–4000 pg/mg. The LC/MS-MS method is effective, sensitive, and robust for the detection of vitamin B3 and its vitamer nicotinamide in human hair samples. This developed hair test can be used in clinical examination to complement blood and urine tests for the long-term deficiency, detection, and quantification of nicotinamide.

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