衰老的角质形成细胞合并黑色素小体导致能量代谢减少导致黑色素积累

IF 3.9 3区 医学 Q2 CELL BIOLOGY
Hiroko Yamazaki, Hideya Ando
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引用次数: 0

摘要

在太阳色素体中,一种典型的与年龄有关的皮肤色素紊乱,大量的黑色素沉积在角质形成细胞的基底层,而不是自发消除。黑色素在角质形成细胞中长期积累的原因尚不完全清楚。因此,我们将重点放在合并黑色素小体(合成黑色素的专门细胞器)的角质形成细胞的能量代谢上,并研究了黑色素在角质形成细胞中积累的机制。通过测量ATP水平、乳酸生成和耗氧量来评估添加黑素体后角质形成细胞的能量代谢。在显微镜下观察添加黑素体后的能量限制。合并黑素体的细胞进行衰老和增殖标记染色。结果表明,黑色素小体掺入后,角质形成细胞的能量代谢上调,能量限制增加了每个细胞的黑色素量。衰老相关β-半乳糖苷酶(细胞衰老标志物)阳性的角质形成细胞积累了大量的黑色素,而增殖标志物5-乙基-2′-脱氧尿苷阳性的角质形成细胞含有很少的黑色素。这些发现表明,衰老的角质形成细胞倾向于积累黑色素,这可能是由于它们的能量代谢受损,因此在黑色素小体结合后无法激活能量代谢。我们的研究结果表明,衰老角质形成细胞的黑色素小体结合导致太阳晶状体中持续的黑色素沉积。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Incorporation of Melanosomes by Senescent Keratinocytes Causes the Accumulation of Melanin due to Decreased Energy Metabolism

The Incorporation of Melanosomes by Senescent Keratinocytes Causes the Accumulation of Melanin due to Decreased Energy Metabolism

In solar lentigo, a typical age-related pigmentary disorder of the skin, abundant melanin is deposited in the basal layer of keratinocytes and not spontaneously eliminated. The reason for the prolonged melanin accumulation in keratinocytes is not fully understood. Therefore, we focused on the energy metabolism of keratinocytes that incorporate melanosomes, specialized organelles where melanin pigment is synthesized, and investigated the mechanism of melanin accumulation in keratinocytes. Energy metabolism in keratinocytes after the addition of melanosomes was assessed by measuring ATP levels, lactate production, and oxygen consumption rate. Energy limitations after melanosome addition were evaluated by microscopy. Cells with incorporated melanosomes were stained for senescence and proliferation markers. The results showed that keratinocytes upregulated their energy metabolism after melanosome incorporation and energy limitations increased the amount of melanin per cell. Keratinocytes positive for senescence-associated β-galactosidase, a cellular senescence marker, accumulated large amounts of melanin, while keratinocytes positive for 5-ethynyl-2′-deoxyuridine, a proliferation marker, contained little melanin. These findings indicate that senescent keratinocytes tend to accumulate melanin, which may be due to their impaired energy metabolism and thus inability to activate energy metabolism after melanosome incorporation. Our results suggest that melanosome incorporation by senescent keratinocytes causes the persistent melanin deposition in solar lentigo.

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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
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