BACKGROUND. Hair follicle preservation for the purpose of delayed applicati
on would help us to transplant hair follicles more efficiently.
METHODS. Isolated single hair follicles were preserved at 4 degrees C in fo
ur different solutions. Viability of preserved follicles was judged by orga
n culture and cell culture. In addition, a small number of hair follicles w
ere transplanted into athymic mice.
RESULTS. By cell culture, both dermal papilla and outer root sheath cells c
ould be cultivated after 7 days of preservation. Hair follicles preserved f
or 48 hours showed a significant increase of hair shafts in organ culture.
Those preserved for 7 days regrew well when transplanted into athymic mice.
CONCLUSION. Preservation of hair follicles at 4 degrees C could be one opti
on to prepare many follicular units at one time for transplantation.