Kippenberger S, Bernd A, Bereiter-Hahn J, Ramirez-Bosca A, Kaufmann R, Holzmann H
Abteilung 1, Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt/Main, Germany.
Pigment Cell Res. 1996 Aug;9(4):179-84. doi: 10.1111/j.1600-0749.1996.tb00107.x.
Eumelanogenesis of human skin melanocytes requires at least three enzymes: tyrosinase, TRP 1, and TRP 2. The regulation of these enzymes on transcriptional level was detected in a semiquantitative attempt. The total RNA of melanocytes was reverse-transcripted and followed by a PCR with degenerated primers for all three enzymes. The amplification products were related to each other densitometrically. We examined five different culture conditions: 1) melanocytes in a popular phorbolester containing F-10-medium, 2) melanocytes in a co-culture medium with EGF, 3) melanocytes in a co-culture medium with high calcium, 4) melanocytes co-cultured with keratinocytes in EGF containing co-culture medium, and 5) melanocytes co-cultured with keratinocytes in co-culture medium with high calcium. Melanocytes cultured in phorbolester containing F-10-medium featured transcripts of tyrosinase, TRP 1, and TRP 2 in the ratio 45:45:10. The same results were obtained for melanocytes co-cultured with keratinocytes under the two different culture conditions. In melanocytes cultured alone in co-culture media only TRP 1-transcripts were present. It is likely that under co-culture conditions a keratinocyte-derived factor supports the transcription of all three enzymes. For melanocytes in the phorbolester-containing melanocyte medium a proteinkinase C dependent regulation of transcription seems possible.
酪氨酸酶、TRP 1和TRP 2。对这些酶在转录水平上的调控进行了半定量检测。黑素细胞的总RNA进行逆转录,然后用针对所有三种酶的简并引物进行PCR。对扩增产物进行光密度分析比较。我们检测了五种不同的培养条件:1)在含有佛波酯的F - 10培养基中的黑素细胞;2)与表皮生长因子共培养的培养基中的黑素细胞;3)高钙共培养培养基中的黑素细胞;4)在含表皮生长因子的共培养培养基中与角质形成细胞共培养的黑素细胞;5)在高钙共培养培养基中与角质形成细胞共培养的黑素细胞。在含有佛波酯的F - 10培养基中培养的黑素细胞,酪氨酸酶、TRP 1和TRP 2的转录本比例为45:45:10。在两种不同培养条件下与角质形成细胞共培养的黑素细胞也得到了相同结果。在共培养培养基中单独培养的黑素细胞仅存在TRP 1转录本。在共培养条件下,角质形成细胞衍生的因子可能支持所有三种酶的转录。对于含佛波酯的黑素细胞培养基中的黑素细胞,转录的蛋白激酶C依赖性调控似乎是可能的。