TITLE
Enhanced in vitro hair growth at the air-liquid interface: minoxidil preserves the root sheath in cultured whisker follicles.

AUTHOR
Waldon DJ; Kawabe TT; Baker CA; Johnson GA; Buhl AE

ORGANISATION
Upjohn Laboratories, Department of Dermatology Research, Kalamazoo, Michigan 49001.

SOURCE
In Vitro Cell Dev Biol Anim 1993 Jul; 29A (7): 555-61

LANGUAGE OF PUBLICATION
English

ABSTRACT
Inasmuch as hair follicles are difficult to maintain in culture, the study of hair biology using cultured hair follicles has met with only limited success. In our attempts to solve the problem of follicle degeneration, we cultured follicles at the air-surface interface on a modified collagen matrix (Gelfoam). In follicles cultured at the air-surface or submerged, we examined follicular morphology, hair shaft growth, sulfotransferase levels, cysteine incorporation, an expression of a tissue inhibitor of metalloproteinase (TIMP), and ultra-high sulfur keratin (UHSK). Follicles cultured at the air-liquid interface produced a 2.7-fold increase in hair growth and maintained an anagen-like morphology. Substrates such as nylon mesh seeded with fibroblasts, Full Thickness Skin, or 5-microns polycarbonate filter also supported hair growth, whereas Gelfilm, GF-A glass filter, filter paper, or 1-micron polycarbonate filter did not. The UHSK expression was significantly higher in the air-liquid interface cultures compared to the submerged culture. Several potassium channel openers, including minoxidil, a minoxidil analog, and the pinacidil analog (P-1075), all stimulated significant cysteine incorporation in follicles. Minoxidil and its analog specifically preserved the follicular root sheath, in contrast to P-1075 which did not, indicating a difference in the two drug types. The preservation of the root sheath was measured by increased TIMP expression and sulfotransferase activity and indicates that the root sheath is a target tissue for minoxidil. Our results show that follicles cultured at the air-liquid interface maintain a better morphology and produced greater hair growth than follicles cultured on tissue culture plastic. (AUTHOR)

MJTR: Hair GD. Minoxidil PD. Vibrissae CY.

MNTR: Air. Animal. Cells, Cultured. Collagenases AI. Comparative Study. Cysteine ME. Gelatin Sponge, Absorbable. Glycoproteins AN. Glycoproteins ME. Guanidines PD. Hair CH. Hair ME. Keratin AN. Keratin ME. Mice. Pyridines PD. Sulfotransferases AN. Sulfotransferases ME. Vibrissae CH. Vibrissae ME. JOURNAL ARTICLE

RNUM: EC 2.8.2 (Sulfotransferases); EC 3.4.24.- (Collagenases); 0 (Gelatin Sponge, Absorbable); 0 (Glycoproteins); 0 (Guanidines); 0 (Pyridines); 0 (Tissue Inhibitor of Metalloproteinases); 38304-91-5 (Minoxidil); 4371-52-2 (Cysteine); 60559-98-0 (P 1075); 68238-35-7 (Keratin)

GEOT: UNITED STATES

IDEN: ISSN: 1071-2690. JOURNAL-CODE: BZE. ENTRY-DATE: 930917. JOURNAL-SUBSET: M. IM-DATE: 9311. PAGE 2 National Library of Medicine MEDLINE Database

ACCE: 93359432