The viability of isolated secondary anagen hair follicles from Angora
goats was studied in an in vitro tissue culture system. Intact hair fo
llicles were isolated from the dermal layer singly or in groups using
watchmakers' forceps under a dissecting microscope following removal o
f both the epidermis at the basal layer and subcutaneous fat layers us
ing a scalpel blade. The connective tissue sheath surrounding the foll
icle and the dermal papilla in the bulb were left intact. The isolated
follicles were maintained floating in supplemented Williams E medium
and showed significant increases in hair shaft length over 96 h. The v
iability of the cultured hair follicles was verified by the findings t
hat (1) the rate of hair shaft elongation was similar to that occurrin
g in vivo; (2) the pattern of DNA synthesis observed by autoradiograph
y of [methyl-H-3]thymidine uptake was maintained in the isolated folli
cles throughout culture; (3) the ATP content was significantly higher
in growing follicles compared with that observed in freshly isolated f
ollicles; and (4) Feulgen-stained preparations of fresh and maintained
hair follicles confirmed the retention of mitotic activity in the mat
rix cells of the bulb for a maximum of 120 h of maintenance.