Thody A J, Graham A
Department of Dermatology, Medical School, University of Newcastle upon Tyne, United Kingdom.
Pigment Cell Res. 1998 Oct;11(5):265-74. doi: 10.1111/j.1600-0749.1998.tb00735.x.
Over the years there has been much debate as to whether alpha-MSH has a role as a pigmentary hormone in humans. There are two main reasons for this. First, despite the observations in the 1960s that alpha-MSH increased skin darkening in humans, there are reports that the peptide has no effect on melanogenesis in cultured human melanocytes. Second, the human pituitary, unlike that of most mammals, secretes very little alpha-MSH and circulatory levels of the peptide in humans are extremely low. However, there is now evidence from several groups that alpha-MSH is capable of stimulating melanogenesis in cultured human melanocytes. Rather than producing an overall increase in melanin production, it appears that the peptide acts specifically to increase the synthesis of eumelanin. Such an action could well explain the previously observed skin darkening effects of alpha-MSH. It is also now known that alpha-MSH is not produced exclusively in the pituitary but has been found at numerous sites, including the skin where it is produced by several cell types. Related Proopiomelanocortin (POMC) peptides such as ACTH are also produced in human skin. The ACTH peptides act at the same receptor (MC-1) as alpha-MSH and certain of these would appear to be more potent than alpha-MSH in stimulating melanogenesis. The ACTH peptides are also present in greater amounts than alpha-MSH in human epidermis and it is likely that they play an important role in regulating pigmentary responses. These POMC peptides are released from keratinocytes in response to ultraviolet radiation (UVR) and it has been proposed that they serve as paracrine factors in mediating UV induced pigmentation. Their production by keratinocytes could therefore be critical in determining pigmentary responses and any changes in the availability of these POMC peptides might explain the variations in tanning ability seen in different individuals. However, the possibility that tanning ability is also dependent upon differences at the level of the MC-1 receptor cannot be ruled out and it has been suggested that an inability to tan may depend upon the presence of non-functional changes at the MC-1 receptor. alpha-MSH does, of course, affect human melanocytes in several ways and its stimulation of melanogenesis could be the consequence of some other fundamental action in the melanocyte. The peptide also has many other target sites in the skin and while it may have a role in regulating skin pigmentation in humans, it should not be viewed solely as a pigmentary peptide. alpha-MSH clearly has many different actions and its primary role in the skin may be to maintain homeostasis.
多年来,关于α-促黑素(α-MSH)在人类中是否作为一种色素生成激素一直存在诸多争议。主要有两个原因。其一,尽管在20世纪60年代观察到α-MSH可使人类皮肤变黑,但有报道称该肽对培养的人类黑素细胞的黑素生成没有影响。其二,与大多数哺乳动物不同,人类垂体分泌的α-MSH极少,且该肽在人体中的循环水平极低。然而,现在有几个研究小组提供的证据表明,α-MSH能够刺激培养的人类黑素细胞的黑素生成。该肽似乎并非导致黑色素生成全面增加,而是特异性地作用于增加真黑素的合成。这样的作用很可能解释了之前观察到的α-MSH对皮肤的变黑效应。现在还知道,α-MSH并非仅在垂体中产生,而是在许多部位都有发现,包括皮肤,在皮肤中它由多种细胞类型产生。相关的阿黑皮素原(POMC)肽,如促肾上腺皮质激素(ACTH)也在人类皮肤中产生。ACTH肽与α-MSH作用于相同的受体(MC-1),并且其中某些肽在刺激黑素生成方面似乎比α-MSH更有效。在人类表皮中,ACTH肽的含量也比α-MSH多,它们很可能在调节色素生成反应中起重要作用。这些POMC肽在角质形成细胞受到紫外线辐射(UVR)时释放,有人提出它们作为旁分泌因子介导紫外线诱导的色素沉着。因此,角质形成细胞产生这些肽对于确定色素生成反应可能至关重要,并且这些POMC肽可用性的任何变化都可能解释不同个体晒黑能力的差异。然而,晒黑能力也取决于MC-1受体水平差异的可能性不能排除,有人认为无法晒黑可能取决于MC-1受体存在无功能变化。当然,α-MSH确实以多种方式影响人类黑素细胞,其对黑素生成的刺激可能是黑素细胞中某些其他基本作用的结果。该肽在皮肤中还有许多其他靶点,虽然它可能在调节人类皮肤色素沉着中起作用,但不应仅将其视为一种色素生成肽。α-MSH显然有许多不同的作用,其在皮肤中的主要作用可能是维持体内平衡。