Growth Factors Influencing the Morphology and Growth Rate of Hair Follicles in a Human Hair Organ Culture.
- Author:
Yoon Sung KIM
;
Kyung Hoon KIM
;
Woo Jae LEE
;
Ji Won JUNG
;
Kyae Yong SONG
;
Ki Beom SUHR
;
Jeung Hoon LEE
;
Jang Kyu PARK
- Publication Type:Original Article
- Keywords:
Hair organ culture;
Human hair
- MeSH:
Atmosphere;
Biology;
Epidermal Growth Factor;
Hair Follicle*;
Hair Removal;
Hair*;
Humans*;
Hydrocortisone;
Insulin;
Intercellular Signaling Peptides and Proteins*;
Organ Culture Techniques*;
Pharmacology;
Physiology;
Selenious Acid;
Sheep;
Sodium Selenite;
Toxicology;
Transferrin
- From:Korean Journal of Dermatology
1998;36(2):210-216
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: In order to study hair biology, a hair organ culture system is necessary. However satisfactory hair culture systems have not been established. OBJECTIVE: The purpose of this study was to examine the effectiveness of growth factors and to establish a hair organ culture system for studying hair biology and to evaluate the effectiveness of growth factors. METHOD: After the healthy human anagen hair follicles were collected without any visible damage, they were cultured in William E medium with several combinations of growth factors including insulin, hydrocortisone, sodium selenite, human transfemn, fetal calf serum and epidermal growth factor at 37C in an atmosphere of 5% CO2/air incubation. The culture medium was changed every 3 days. The results were evaluated by measuring hair growth and hair follicle morphology. RESULTS: The results of this study are summarized as follows; 1) In the medium composed of insulin, hydrocortisone,sodium selenite and human transferrin, the human hair follicles continued to grow at an in vivo rate of 0.3mm in a day over 10 days without change of gross and microscopic morphology. 2) In the medium containing insulin and/or hydrocortisone the growing rate of the human hair follicles was similar to that in vivo, but the follicles revealed premature entry into catagen at 2-6 days in the culture macroscopically and microscopically. 3) Adding fetal calf serum to the above medium made the hair follicles retain the freshly isolated hair follicles morphology for 10 days in culture, even though they grew somewhat slower than the in vivo rate from 6 days in culture. 4) The effectiveness of EGF mimics the in vivo depilation of EGF in sheep. CONCLUSION: To supplement insulin, hydrocortisone, sodium selenite, transferrin as growth factors, William E medium was necessary for maintenance of an in vivo growth rate and the morphology the anagen hair follicles. This culture system is not enough, but it might be useful for investigation of the physiology, biology of hair follicles as well as pharmacology and toxicology in hair.
