Werkmeister J R, Merryman J I, McCauley L K, Horton J E, Capen C C, Rosol T J
Department of Veterinary Pathobiology, Ohio State University, Columbus 43210.
Exp Cell Res. 1993 Sep;208(1):68-74. doi: 10.1006/excr.1993.1223.
The role of parathyroid hormone-related protein (PTHrP) and its regulation in normal epidermal physiology is not currently known. Recent evidence suggests that PTHrP production may be related to the degree of differentiation of keratinocytes in vitro. This investigation characterized the production of PTHrP by normal human foreskin keratinocytes (NHFK) during both spontaneously occurring and induced differentiation in vitro. PTHrP production in keratinocyte serum-free conditioned medium was determined using an N-terminal radioimmunoassay for human PTHrP (1-36). Agents known to stimulate (calcium, 1,25-dihydroxyvitamin D3) or inhibit (transforming growth factor-beta) keratinocyte differentiation were examined for their ability to alter production of PTHrP. Measurements of cell number and involucrin content of the cultures were made to confirm the effects of these agents on keratinocyte growth and differentiation. The production of PTHrP in control cultures (under low calcium conditions, 0.08 mM) was decreased and involucrin content increased (P < 0.01) after the cells became confluent. The addition of 1 mM calcium to keratinocyte medium increased cell number and involucrin content of the cultures (P < 0.05) but inhibited production of PTHrP (P < 0.01). The 1,25-dihydroxyvitamin D3 (10 nM) had no significant effect on cell number or PTHrP production, but increased involucrin content (P < 0.05). Transforming growth factor-beta (5 ng/ml) decreased both cell number (P < 0.05) and involucrin content (P < 0.01), but significantly stimulated PTHrP production (P < 0.01). These data indicate that the production of PTHrP by NHFK is inhibited with the onset of both spontaneously occurring and calcium-induced differentiation in vitro, while transforming growth factor-beta inhibited differentiation and upregulated PTHrP production in normal human keratinocytes.
甲状旁腺激素相关蛋白(PTHrP)在正常表皮生理中的作用及其调控目前尚不清楚。最近的证据表明,PTHrP的产生可能与体外角质形成细胞的分化程度有关。本研究对正常人包皮角质形成细胞(NHFK)在体外自发分化和诱导分化过程中PTHrP的产生进行了表征。使用针对人PTHrP(1-36)的N端放射免疫测定法测定角质形成细胞无血清条件培养基中PTHrP的产生。研究了已知能刺激(钙、1,25-二羟基维生素D3)或抑制(转化生长因子-β)角质形成细胞分化的试剂改变PTHrP产生的能力。对培养物的细胞数量和内披蛋白含量进行测量,以确认这些试剂对角质形成细胞生长和分化的影响。在细胞汇合后,对照培养物(低钙条件下,0.08 mM)中PTHrP的产生减少,内披蛋白含量增加(P < 0.01)。向角质形成细胞培养基中添加1 mM钙可增加培养物的细胞数量和内披蛋白含量(P < 0.05),但抑制PTHrP产生(P < 0.01)。1,25-二羟基维生素D3(10 nM)对细胞数量或PTHrP产生无显著影响,但增加了内披蛋白含量(P < 0.05)。转化生长因子-β(5 ng/ml)降低了细胞数量(P < 0.05)和内披蛋白含量(P < 0.01),但显著刺激了PTHrP产生(P < 0.01)。这些数据表明,在体外自发分化和钙诱导分化开始时,NHFK产生PTHrP受到抑制,而转化生长因子-β在正常人角质形成细胞中抑制分化并上调PTHrP产生。