Ann Dermatol.  2016 Oct;28(5):533-539. 10.5021/ad.2016.28.5.533.

Isolation and Quantification of Glycosaminoglycans from Human Hair Shaft

Affiliations
  • 1Department of Pharmacology, University of Athens School of Medicine, Athens, Greece. elenimaniat@yahoo.com

Abstract

BACKGROUND
There is evidence that glycosaminoglycans (GAGs) are present in the hair shaft within the follicle but there are no studies regarding GAGs isolation and measurement in the human hair shaft over the scalp surface, it means, in the free hair shaft.
OBJECTIVE
The purpose of our research was to isolate and measure the total GAGs from human free hair shaft.
METHODS
Seventy-five healthy individuals participated in the study, 58 adults, men and women over the age of 50 and 17 children (aged 4~9). GAGs in hair samples, received from the parietal and the occipital areas, were isolated with 4 M guanidine HCl and measured by the uronic acid-carbazole reaction assay.
RESULTS
GAGs concentration was significantly higher in the occipital area than in the parietal area, in all study groups. GAG levels from both areas were significantly higher in children than in adults. GAG levels were not associated with gender, hair color or type.
CONCLUSION
We report the presence of GAGs in the human free hair shaft and the correlation of hair GAG levels with the scalp area and participants' age.

Keyword

Glycosaminoglycans; Hair; Proteoglycans

MeSH Terms

Adult
Child
Female
Glycosaminoglycans*
Guanidine
Hair Color
Hair*
Humans*
Male
Proteoglycans
Rabeprazole
Scalp
Glycosaminoglycans
Guanidine
Proteoglycans

Reference

1. Bernard BA. Hair cycle dynamics: the case of the human hair follicle. J Soc Biol. 2003; 197:57–61.
2. Couchman JR. Rat hair follicle dermal papillae have an extracellular matrix containing basement membrane components. J Invest Dermatol. 1986; 87:762–767.
Article
3. Chiu HC, Chang CH, Chen JS, Jee SH. Human hair follicle dermal papilla cell, dermal sheath cell and interstitial dermal fibroblast characteristics. J Formos Med Assoc. 1996; 95:667–674.
4. Braun Falco O. The histochemistry of the hair follicle. In : Montagna W, Ellis RA, editors. The biology of hair growth. Providence, RI: Academic Press;1958. p. 65–90.
5. Schmid K, Grundboeck-Jusco J, Kimura A, Tschopp FA, Zollinger R, Binette JP, et al. The distribution of the glycosaminoglycans in the anatomic components of the lung and the changes in concentration of these macromolecules during development and aging. Biochim Biophys Acta. 1982; 716:178–187.
Article
6. Gniadecka M, Faurskov Nielsen O, Christensen DH, Wulf HC. Structure of water, proteins, and lipids in intact human skin, hair, and nail. J Invest Dermatol. 1998; 110:393–398.
Article
7. Paulsson M. Basement membrane proteins: structure, assembly and cellular interactions. Crit Rev Biochem Mol Biol. 1992; 27:93–127.
Article
8. Couchman JR. Hair follicle proteoglycans. J Invest Dermatol. 1993; 101:60–64.
Article
9. du Cros DL, LeBaron RG, Couchman JR. Association of versican with dermal matrices and its potential role in hair follicle development and cycling. J Invest Dermatol. 1995; 105:426–431.
Article
10. Kloska A, Bohdanowicz J, Konopa G, Tylki-Szymńska A, Jakóbkiewicz-Banecka J, Czartoryska B, et al. Changes in hair morphology of mucopolysaccharidosis I patients treated with recombinant human alpha-L-iduronidase (laronidase, Aldurazyme). Am J Med Genet A. 2005; 139:199–203.
11. Hinek A, Wilson SE. Impaired elastogenesis in Hurler disease: dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly. Am J Pathol. 2000; 156:925–938.
12. Malgouries S, Thibaut S, Bernard BA. Proteoglycan expression patterns in human hair follicle. Br J Dermatol. 2008; 158:234–242.
Article
13. Kirschbaum C, Tietze A, Skoluda N, Dettenborn L. Hair as a retrospective calendar of cortisol production-increased cortisol incorporation into hair in the third trimester of pregnancy. Psychoneuroendocrinology. 2009; 34:32–37.
Article
14. Carney LS. Proteoglycans. In : Chaplin MF, Kennedy JF, editors. Carbohydrate analysis: a practical approach. Oxford: Oxford University Press;1987. p. 97–142.
15. Carrino DA, Sorrell JM, Caplan AI. Age-related changes in the proteoglycans of human skin. Arch Biochem Biophys. 2000; 373:91–101.
Article
16. Jung JW, Cha SH, Lee SC, Chun IK, Kim YP. Age-related changes of water content in the rat skin. J Dermatol Sci. 1997; 14:12–19.
Article
17. Bitter T, Muir HM. A modified uronic acid carbazole reaction. Anal Biochem. 1962; 4:330–334.
Article
18. Dische Z. A new specific color reaction of hexuronic acids. J Biol Chem. 1947; 167:189–198.
Article
19. Randall VA. Androgens and hair growth. Dermatol Ther. 2008; 21:314–328.
Article
20. Kligman AM. The comparative histopathology of male-pattern baldness and senescent baldness. Clin Dermatol. 1988; 6:108–118.
Article
21. Trüeb RM. Pharmacologic interventions in aging hair. Clin Interv Aging. 2006; 1:121–129.
Article
22. Waller JM, Maibach HI. Age and skin structure and function, a quantitative approach (II): protein, glycosaminoglycan, water, and lipid content and structure. Skin Res Technol. 2006; 12:145–154.
Article
23. Randall VA, Thornton MJ, Messenger AG. Cultured dermal papilla cells from androgen-dependent human hair follicles (e.g. beard) contain more androgen receptors than those from non-balding areas of scalp. J Endocrinol. 1992; 133:141–147.
Article
24. Thornton MJ, Taylor AH, Mulligan K, Al-Azzawi F, Lyon CC, O'Driscoll J, et al. The distribution of estrogen receptor beta is distinct to that of estrogen receptor alpha and the androgen receptor in human skin and the pilosebaceous unit. J Investig Dermatol Symp Proc. 2003; 8:100–103.
Article
25. Hibberts NA, Howell AE, Randall VA. Balding hair follicle dermal papilla cells contain higher levels of androgen receptors than those from non-balding scalp. J Endocrinol. 1998; 156:59–65.
Article
26. Richeti F, Kochi C, Rocha MN, Sant'Anna Corrêa C, Lazzarini R, Guazzelli RM, et al. Increased androgen receptor messenger RNA in frontal-parietal hair follicles of women with androgenetic alopecia. Genet Mol Res. 2013; 12:1834–1840.
Article
27. Gustafsson JA. An update on estrogen receptors. Semin Perinatol. 2000; 24:66–69.
Article
28. Bornemann DJ, Duncan JE, Staatz W, Selleck S, Warrior R. Abrogation of heparan sulfate synthesis in Drosophila disrupts the Wingless, Hedgehog and Decapentaplegic signaling pathways. Development. 2004; 131:1927–1938.
Article
29. Mou C, Jackson B, Schneider P, Overbeek PA, Headon DJ. Generation of the primary hair follicle pattern. Proc Natl Acad Sci USA. 2006; 103:9075–9080.
Article
30. Pellegrini L. Role of heparan sulfate in fibroblast growth factor signalling: a structural view. Curr Opin Struct Biol. 2001; 11:629–634.
Article
31. Ota Y, Saitoh Y, Suzuki S, Ozawa K, Kawano M, Imamura T. Fibroblast growth factor 5 inhibits hair growth by blocking dermal papilla cell activation. Biochem Biophys Res Commun. 2002; 290:169–176.
Article
32. Cohen T, Gitay-Goren H, Sharon R, Shibuya M, Halaban R, Levi BZ, et al. VEGF121, a vascular endothelial growth factor (VEGF) isoform lacking heparin binding ability, requires cell-surface heparan sulfates for efficient binding to the VEGF receptors of human melanoma cells. J Biol Chem. 1995; 270:11322–11326.
Article
33. Takada T, Katagiri T, Ifuku M, Morimura N, Kobayashi M, Hasegawa K, et al. Sulfated polysaccharides enhance the biological activities of bone morphogenetic proteins. J Biol Chem. 2003; 278:43229–43235.
Article
34. Catlow K, Deakin JA, Delehedde M, Fernig DG, Gallagher JT, Pavão MS, et al. Hepatocyte growth factor/scatter factor and its interaction with heparan sulphate and dermatan sulphate. Biochem Soc Trans. 2003; 31:352–353.
Article
35. Soma T, Tajima M, Kishimoto J. Hair cycle-specific expression of versican in human hair follicles. J Dermatol Sci. 2005; 39:147–154.
Article
36. Westgate GE, Messenger AG, Watson LP, Gibson WT. Distribution of proteoglycans during the hair growth cycle in human skin. J Invest Dermatol. 1991; 96:191–195.
Article
37. Verdier-Sévrain S. Effect of estrogens on skin aging and the potential role of selective estrogen receptor modulators. Climacteric. 2007; 10:289–297.
Article
38. Su LH, Chen TH. Association of androgenetic alopecia with metabolic syndrome in men: a community-based survey. Br J Dermatol. 2010; 163:371–377.
Article
39. González-González JG, Mancillas-Adams LG, Fernández-Reyes M, Gómez-Flores M, Lavalle-González FJ, Ocampo-Candiani J, et al. Androgenetic alopecia and insulin resistance in young men. Clin Endocrinol (Oxf). 2009; 71:494–499.
Article
40. Skalnaya MG, Tkachev VP. Trace elements content and hormonal profiles in women with androgenetic alopecia. J Trace Elem Med Biol. 2011; 25:Suppl 1. S50–S53.
Article
41. Sylven B. The qualitative distribution of metachromatic polysaccharide material during hair growth. Exp Cell Res. 1950; 1:582–589.
Article
42. Moretti G, Cipriani C, Rebora A, Rampini E, Crovato F. Correlation of tissue mucopolysaccharides with the hair cycle. J Invest Dermatol. 1967; 48:498–503.
43. Saitoh M, Uzuka M, Sakamoto M. Human hair cycle. J Invest Dermatol. 1970; 54:65–81.
Article
44. Bouillon C. Shampoos. Clin Dermatol. 1996; 14:113–121.
Article
Full Text Links
  • AD
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr