Improved method for the isolation and cultivation of human scalp dermal papilla cells.

We present an improved method for the isolation and cultivation of human scalp anagen hair follicle dermal papilla cells. Following treatment of the isolated dermal papilla with collagenase, incubation in Chang's medium mediates accelerated growth of the papilla cells when compared with other media such as DMEM, M199, and EMEM. Upon reaching confluency, the cells cultured in this fashion exhibit a multilayer-forming property that is dependent on normal proteoglycan synthesis. The papilla cells maintain this morphologic behavior for as long as 7 weeks in culture, or after being subcultured six times. During this time, the cells continue to synthesize extracellular matrix components associated with the human anagen follicle in situ. These include chondroitin sulfate, laminin, and type IV collagen. Type III collagen and keratan sulfate are poorly expressed by the papilla both in situ and in vitro. Heparan sulfate proteoglycan, a matrix component of the papilla in situ, is poorly expressed in vitro. Earlier reports suggested that the expression of extracellular matrix components is not maintained in culture. We show that the expression of these molecules is not dependent on the secondary culture medium, but continues in DMEM and M199 after primary culture in Chang's medium. Our results suggest that initial exposure of the dermal papilla to Chang's medium either selectively permits the outgrowth of papilla cells having extracellular matrix components similar to those found in situ, or stabilizes the expression of extracellular matrix components among the entire cultured cell population.

Effect of prostaglandin E2 on cervical compliance in pregnant ewes.

Cervical compliance increases dramatically at parturition in sheep independent of uterine activity. Recently, in vitro production of prostaglandin E2 (PGE2) by the cervix has been shown to increase at parturition. This study investigated the effects of PGE2 on cervical compliance and uterine blood flow in pregnant ewes. Eight animals were chronically instrumented with pressure balloons within the cervical os and amniotic cavity, an electromagnetic flow probe on a uterine artery, and catheters in the maternal cervical os, femoral artery, femoral, uterine, and cervical veins, and fetal hindlimb vein. PGE2 (10 mg) was administered in a water-soluble gel into the cervical os every 4 hours times three doses at least 5 days after surgical preparation (124 to 142 days' gestation). In all eight ewes, cervical compliance increased within 8 to 12 posttreatment hours to levels comparable to that seen at spontaneous parturition. Five of the ewes did not progress into labor; compliance in these ewes returned to baseline 24 to 72 hours after the peak. Uterine blood flow was measured in five ewes during the PGE2 treatment and demonstrated no significant alterations. Maternal cardiovascular and fetal respiratory parameters were monitored throughout the experiment and remained stable. The present data suggest that PGE2 may be an important regulatory of the biochemical and physical changes which occur in the cervix at parturition.