Meningeal Melanocytes in the Mouse: Distribution and Dependence on Mitf
Stefán A. H. Gudjohnsen1,2 
Diahann A. M. Atacho1,2 
Franck Gesbert3,4,5 
Graca Raposo6,7 
Ilse Hurbain6,7 
Lionel Larue3,4,5 
Eirikur Steingrimsson2* 
Petur Henry Petersen1- 1Faculty of Medicine, Department of Anatomy, Biomedical Center, University of Iceland, Reykjavik, Iceland
- 2Faculty of Medicine, Department of Biochemistry and Molecular Biology, Biomedical Center, University of Iceland, Reykjavik, Iceland
- 3Institut Curie, PSL Research University, INSERM U1021, Normal and Pathological Development of Melanocytes, Orsay, France
- 4Université Paris-Sud, Université Paris-Saclay, CNRS UMR 3347, Orsay, France
- 5Equipe Labellisée Ligue Contre le Cancer, Orsay, France
- 6Institut Curie, PSL Research University, Paris, France
- 7CNRS UMR144, Structure and Membrane Compartments, and Cell and Tissue Imaging Facility (PICT-IBiSA), Paris, France
Summary: Melanocytes are pigment producing cells derived from the neural crest. They are primarily found in the skin and hair follicles, but can also be found in other tissues including the eye, ear and heart. Here, we describe the distribution of pigmented cells in C57BL/6J mouse meninges, the membranes that envelope the brain. These cells contain melanosomes of all four stages of development and they depend on Microphthalmia associated transcription factor (MITF), the master regulator of melanocyte development, suggesting that they are bona-fide melanocytes. The location of these pigmented cells is consistent with the location of meningeal melanomas in humans and animal models.
Significance: Here, we document and define pigmented cells in the meninges of the mouse brain and confirm that they are melanocytes. This is important for understanding the role of this cell type and for understanding primary meningeal melanoma, a rare disease that likely arises from normal meningeal melanocytes.
Introduction
Melanocytes are neural crest derived cells that are primarily found in the skin and hair follicles in humans and are largely restricted to the hair follicles in mice. Their function in pigmentation and ultra-violet (UV) response has been well characterized. Melanocytes are also present in other organs such as the eye and inner ear (Colombo et al., 2011). In these tissues, the melanocytes are known to depend on the Microphthalmia associated transcription factor (Mitf). Mice which carry a mutation in the Mitf gene have white coat color due to lack of hair follicle melanocytes (Hodgkinson et al., 1993), they exhibit microphthalmia due to defects in the retinal pigment epithelial cells of the eye (Steingrimsson et al., 2004) and they are deaf due to the pivotal role of melanocytes in the inner ear (Ni et al., 2013).
Melanocytes have been shown to exist in other regions of the body including in the mouse heart (Yajima and Larue, 2008). Pigmented cells have also been described in the meninges of the mouse, rat, cat and humans (Barden and Levine, 1983; Goldgeier et al., 1984; Morse and Cova, 1984; Fetissov et al., 1999). The role of melanocytes in the heart and in the meninges is currently unknown. Also, the histological distribution of meningeal melanocytes and their dependence on MITF, the master regulator of melanocyte development, has not been established. Here, we describe the distribution of pigmented cells in the meninges of mice and demonstrate that they have characteristics of melanocytes as they contain melanosomes and depend on Mitf.
Materials and Methods
Mice
C57BL/6J, C57BL/6-Mitfvga9 and C57BL/6-Tyrc−2J mice were bred and housed in an animal facility at the University of Iceland. The use of laboratory animals was approved by the Icelandic Food and Veterinary Authority (permit ID: 2013-03-01) with all maintenance and handling conducted in accordance with Icelandic law on animal welfare. C57BL/6 mice were also housed in pathogen-free conditions at Institut Curie, conforming to French and European Union legislation.
Examination of Pigment Cells
To examine the meningeal pigment cells, the mice were sacrificed and the calvarium carefully removed (Figure 1A). After the removal of the calvarium, the brain and olfactory bulb were exposed at which point pigmented cells could be observed on top of the olfactory bulb and between the cerebellum and cortex. Next, the brain was carefully removed and pigmented cells observed underneath the olfactory bulb and between the olfactory bulb and cortex. Finally the cranial floor was examined. Inner ear melanocytes were examined by sectioning through the skull as indicated in Figure 1.
Figure 1. Location of meningeal pigment cells as they appear during dissection. (A) Dorsal view of the calvarium after it has been removed, revealing the brain. (B) A dorsal view of the brain after it has been removed from the skull. Melanocytes can be found on top of the olfactory bulb anteriorly (red arrow), between the olfactory bulb and the cortex (blue arrow) and between the cerebellum and cortex posteriorly (green arrow). (C) The ventral aspect of the brain showing pigment cells underneath the olfactory bulb (red arrow). (D) Dorsal view of the cranial floor of the skull after the brain has been removed. Pigmented cells can be seen posteriorly surrounding the pterygopalatine artery where it branches off into the middle meningeal artery lateral to the trigeminal ganglion on either side (green arrow). Anteriorly, pigment cells can be found around the optic and trigeminal nerves where they exit the skull (red arrow). At the bottom of the image are two red lines which indicate where the skull was cut to determine whether inner ear melanocytes were present or not. In all panels, up is anterior and down posterior. Ct, cortex; ob, olfactory bulb; cb, cerebellum; tg, trigeminal ganglion.
Histochemical Staining
For staining of sections of the pterygopalatine artery, whole heads were decalcified, fixed and embedded in paraffin. They were then sectioned and stained either using the standard hematoxylin and eosin stain or the Masson-Hamperl silver stain for melanocytes (Grimelius et al., 1994). A section from a human primary melanoma specimen was used as a positive control for pigmented cells containing melanin.
Electron Microscopy
For transmission electron microscopy (TEM), samples were obtained by careful dissection of the area between the olfactory bulb and the cortex and from the pterygopalatine artery of C57BL/6J mice and fixed overnight in 2.5% (v/v) glutaraldehyde in PBS. The samples were then embedded in resin, trimmed, rough sectioned and stained with toluidine blue. After appropriate sections had been found, thin-sectioned samples of 60–70 nm were post stained with 4% (v/v) aqueous uranyl acetate for 10 min and lead citrate for 1 min. Electron micrographs were acquired on a Tecnai Spirit G2 electron microscope (FEI, Eindhoven, Netherlands) equipped with a 4 k CCD camera (Quemesa, Olympus, Münster, Germany).
RT-PCR
For RT-PCR, C57BL/6J, C57BL/6J-Mitfmi−vga9/Mitfmi−vga9, C57BL/6J-Mitfmi−vga9/+ and C57BL/6J-Tyrc-2J/Tyrc-2J mice were sacrificed and the meninges obtained by carefully removing the brain and subsequently peeling the meninges from the brain around the olfactory bulb. Meninges from three mice per genotype were pooled, and RNA isolated using a phenol-chloroform extraction method (Chomczynski and Sacchi, 1987). Similarly, RNA was isolated from the B16-F1 mouse melanoma cell line after culture in DMEM medium containing 1% Penicillin-streptomycin and 10% Fetal Bovine Serum under standard conditions. cDNA was synthesized using 0.3 ng of total RNA using SuperscriptII RT from Invitrogen (Carlsbad, USA). RT-PCR was performed using HotStart Taq Polymerase from Qiagen (Hilden, Germany). The following primer pairs were used: Mitf-M Forward: 5′-GGAAATGCTAGAATACAGTCACTACC-3′, MITF-M Reverse: 5′-CATGCACGACGCTCGAGAGTGC-3′, Pmel Forward: 5′-ACCTGGGGAAAATACTGGCA-3′, Pmel Reverse: 5′-AGGAAGTGCTTGGTCTCTCC-3′, beta-actin Forward: 5′-CACAGCTGAGAGGGAAATCG-3′, beta-actin Reverse: 5′-GATCTTGATCTTCATGGTGC-3′. Bands were observed at the predicted band size of 337 bp for Mitf-M, 236 bp for Pmel and 382 bp for beta-actin.
Results
Distribution of Pigmented Cells in the Meninges
To determine the distribution of pigmented cells in the meninges of mice, 45 wild type C57BL/6J mice of both sexes, ranging in age from 0.5–19 months, were examined. Dendritic, pigmented cells were found in the following locations: (i) Between the olfactory bulb and the cortex, occasionally extending into the anterior interhemispheric area (blue arrow in Figure 1B); (ii) on top of the olfactory bulb (red arrow in Figure 1B); (iii) between the cerebellum and the cortex (green arrow in Figure 1B); (iv) under the olfactory bulb (red arrow in Figure 1C); (v) around the pterygopalatine and middle meningeal artery at their junction lateral to the trigeminal ganglion (green arrow in Figure 1D); and (vi) around the optic and trigeminal nerves anteriorly (red arrow in Figure 1D). The pigmented cells in the cranial floor meninges are mainly localized around the pterygopalatine artery where it branches off into the middle meningeal artery and at the exit points of the optic and trigeminal nerves from the skull (Figures 2A,D). The pigmented cells in the meninges surround the olfactory bulb (Figures 3A,D,G), and are found between the cerebellum and cortex. These pigmented cells were also observed in C57BL/6J mice housed in Orsay, France.
Figure 2. Pigmented cells in the cranial floor. (A–C) The pterygopalatine artery where it branches off into the middle meningeal artery in wild type, Mitfvga9/+ and Mitfvga9/Mitfvga9 mice. (D–F) The trigeminal nerve and the exit point for the optic nerve and the optic nerve in wild type, Mitfvga9/+ and Mitfvga9/Mitfvga9 mice. Arrows point to the pigmented cells. In all panels, left is posterior and right anterior. Tg, trigeminal ganglion; pp, pterygopalatine artery. Scale bar represents 1 mm.
Figure 3. Pigmented cells around the olfactory bulb. (A–C) A dorsal view of the olfactory bulb in wild type, Mitfmi−vga9/+ and Mitfmi−vga9/Mitfmi−vga9 mice. The insert in (A) shows a greater magnification of a portion of the image. Anterior is to the right. (D–F) Dorsal view of the area between the olfactory bulb and cortex in wild type, Mitfmi−vga9/+ and Mitfmi−vga9/Mitfmi−vga9 mice. (G–I) A ventral view of the brain and in particular the olfactory bulb in wild type, Mitfmi−vga9/+ and Mitfmi−vga9/Mitfmi−vga9 mice. Arrows point towards pigment cells. Anterior is up in (D–I). Scale bars represent 1mm.
Pigmented cells were most abundant around the olfactory bulb and surrounding the pterygopalatine artery in the cranial floor (Figures 2, 3). However, we noticed that the presence of pigmented cells in the different regions varied between animals of the isogenic C57BL/6J strain. In order to determine the prevalence of pigmented cells in the different areas, the number of mice containing pigmented cells in the different regions was determined. Table 1 shows the prevalence of pigment containing cells in the cranial floor and inner ear. In wild type mice, the inner ear and left and right optic nerves nearly always contain pigmented cells. They are common but less frequently observed around the left and right blood vessels (Table 1). Table 2 shows the distribution of pigmented cells around the brain. In wild type mice the ventral olfactory bulb and the region between the olfactory bulb and cortex frequently have pigmented cells but they are less frequently observed on the dorsal olfactory bulb and in the region between the cerebellum and cortex (Table 2). The pigmented cells were sometimes present only on the left side of the animal and sometimes only on the right side. In order to quantify this we analyzed their bilateral distribution. Table 3 shows whether the cells are unilaterally distributed, bilaterally distributed or absent from each area. These cells are bilaterally present in the inner ear, optic nerve and ventral olfactory bulb but are either not present or unilaterally present on either the left or right side around the blood vessel, between the cerebellum and cortex and on the dorsal side of the olfactory bulb.
Table 1. Distribution of meningeal pigment cells in the cranial floor and inner ear of mice.
Table 2. The distribution of pigment cells in the meninges around the brain and olfactory bulb.
Table 3. The distribution of pigment cells: unilateral vs. bilateral in wild type.
Distribution of Pigment Cells Varies with Age
To determine whether age had an effect on the distribution of these cells, the wild type C57BL/6J mice were divided into three groups, each with 15 mice: young (under 2 months), adult (between 2 and 8 months) and old (older than 8 months old). The presence and distribution of pigmented cells was determined in each area for each age group (Tables 4, 5). Pigmented cells were nearly always observed in the inner ear. Fewer old mice had pigmented cells in the optic nerve area than were seen in young or adult mice, suggesting that these cells disappear from these areas with age (Table 4). The prevalence of pigmented cells around the meningeal blood vessels did not change with age. Interestingly, we observed that pigmented cells were more common on top of the olfactory bulb in young mice (45.5% of the mice show pigmented cells in this area—average of left and right side) than in older mice (19%). In contrast, pigment cells were more prevalent on the ventral olfactory bulb in old mice (94%) than in young mice (59.5%).
Table 4. The distribution of pigmented cells in the cranial floor and in the inner ear by age group.
Table 5. The distribution of pigmented cells in the meninges surrounding the brain and olfactory bulb.
Pigmented Cells in the Meninges Depend on Mitf
To determine whether the pigmented cells in the meninges depend on Mitf expression, their presence and distribution was determined in C57BL/6-Mitfmi−vga9 homo- and heterozygous mice. Mitfmi−vga9/+ mice contain melanocytes in the inner ear and meningeal pigment cells below the olfactory bulb and between the olfactory bulb and the cortex (Figures 2B,E, 3B,E,H; Tables 1, 2). However, the pigmented cells were missing from all other areas of the brain examined. Importantly, in the homozygous C57BL/6-Mitfmi−vga9/Mitfmi−vga9 mice, no pigmented cells were present, demonstrating that the inner ear and meningeal pigment cells depend on Mitf (Figures 2C,F, 3C,F,I; Tables 1, 2). Pigmented cells were not observed in C57BL/6J-albino mice (C57BL/6J-Tyrc-2J/Tyrc-2J) which do not produce melanin.
To determine whether the M-Mitf (encoding a melanocyte specific isoform of Mitf) and Pmel (encoding a type I transmembrane glycoprotein) genes, two genetic markers for melanocytes, are expressed in mouse meninges, RT-PCR was performed on meninges isolated from C57BL/6J, C57BL/6J-Tyrc-2J/Tyrc-2J and C57BL/6J-Mitfmi−vga9/Mitfmi−vga9 mice, using B16 mouse melanoma cells as a positive control. Since melanin has been shown to inhibit RNA and cDNA preparations (Eckhart et al., 2000), C57BL/6J-Tyrc-2J/Tyrc-2J mice, which have melanocytes but do not make melanin, were used as an additional source of meningeal tissue. All samples were positive for Actin. As expected, the B16 melanoma cell line, as well as the meninges from C57BL/6J and C57BL/6J-Tyrc-2J/Tyrc-2J mice, were positive for Mitf-M and Pmel (Figure 4A). However, RT-PCR performed on C57BL/6J-MITFmi−vga9/Mitfmi−vga9 mice showed absence of both Mitf and Pmel transcripts (Figure 4A). Therefore the presence of melanocyte specific Mitf-M and its downstream target Pmel further suggests the presence of bona fide melanocytes in the meninges isolated from the mouse olfactory bulb.
Figure 4. Location of melanocytes around the pterygopalatine artery. (A) RT-PCR performed on cDNA obtained from B16 mouse melanoma cells as positive control, olfactory bulb meninges from C57Bl/J6, B6Tyrc-2J/Tyrc-2J and Mitfmi−vga9/Mitfmi−vga9 mice and no-cDNA negative control. Primers used were for Mitf-M, Pmel, and Actin. (B) A coronal section of the pterygopalatine artery stained with H&E. (C) An image of an adjoining section stained with Masson-Hamperl silverstain to detect the presence of melanin. Pp, pterygopalatine artery. Scale bars represent 100 μm.
The Pigmented Cells are Melanocytes
The pigment containing cells have stellate morphology, they are dendritic and depend on Mitf, all typical characteristics of melanocytes. The mammalian brain coverings consist of three layers of protective tissue, namely the dense collgenous dura, the arachnoid and the pia, the latter two collectively called the leptomeninges. In order to determine in which cell layer the pigmented cells are located, we utilized classical histochemical staining techniques to stain tissues located between the olfactory bulb and cerebral cortex and around the pterygopalatine artery. Both the hematoxylin-eosin (H&E) and Masson-Hamperl (specific for melanin) stains showed darkly pigmented cells located within the leptomeninges between the olfactory bulb and cerebral cortex and surrounding the pterygopalatine artery (Figures 4B,C). To characterize these cells further, we used TEM to determine whether they contain melanosomes of all stages and had not simply phagocytosed extracellular melanin. Pigment cells from both the olfactory region and the pterygopalatine region were examined. Examination with TEM revealed that in both regions the pigmented cells contained melanosomes of all four stages of development (Figure 5).
Figure 5. Transmission electron microscopy of pigment cells. Morphology of melanocytes (A,B) and melanosomes (C–E) in olfactory bulb at the electron microscope level. Asterisks in (A) denote melanocytes or dendrites of melanocytes. Stage I (I), stage II (II) and stage III melanosomes (III) can be seen between a large number of stage IV melanosomes (B–E). m: mitochondria. The scale bar represents 5 μm in (A), 2 μm in (B) and 500 nm in (C–E).
Discussion
Here, we describe the location of pigmented, dendritic cells in the brain coverings of the mouse as well as proximal to the optic nerve. These cells are found in six distinct areas of the meninges in C57BL/6J mice, they contain all stages of melanosomes and they express Mitf. They are not visible in albino mice suggesting that their pigment depends on tyrosinase. Also, they are not found in homozygous Mitfmi−vga9 mice, demonstrating that the presence of these cells depends on this master regulator of melanocyte development and differentiation. Interestingly, fewer pigmented cells were observed in Mitfmi−vga9 heterozygotes suggesting that these cells are sensitive to the loss of Mitf activity. These observations strongly suggest that these pigmented cells in the meninges are melanocytes. Only one of the areas we showed to contain melanocytes, the area between the olfactory bulb and the cortex, has previously been described to contain pigment cells in the mouse (Markert and Silvers, 1956; Barden and Levine, 1983). Barden and Levine (1983) reported the distribution of pigmented cells in the rat similar to that illustrated here. Pigmented cells have also been described in the meninges of other mammals (Goldgeier et al., 1984; Morse and Cova, 1984; Fetissov et al., 1999). Their distribution seems to vary between species. However they are always to some extent associated with the meningeal vasculature. This location is consistent with the angiotropism observed for melanoma cells and may suggest that melanocytes can travel along this route (Lugassy et al., 2014). At present, we do not have an explanation for the variation in the presence of these cells in the different areas of the brain. Age appears to be a factor. Local variations in the presence of melanocytes have not been reported for other tissues. In mouse heart valves and septa the number of melanocytes has been shown to be related to that in the skin (Yajima and Larue, 2008). A similar relationship with skin pigmentation has been observed in meningeal melanocytes of Ugandan Africans (Lewis, 1969). More detailed analysis of melanocyte distribution in different tissues may reveal previously undetected variation.
Melanocytes are derived from neural crest cells, known for their multipotency and migration ability during development. Using in situ hybridization analysis, Baxter and Pavan (2003) showed cells expressing Pmel, a melanoblast marker, at the dorsal surface of the midbrain/hindbrain boundary and extending laterally and along the lateral surface of the forebrain/midbrain boundary during development. They showed that these cells depend on Mitf. Similar cranial neural crest cells have been described in chickens (Baker et al., 1997). The meningeal melanocytes described here are likely to arise from the cranial neural crest. Alternatively, they may be derived from neural crest derivatives such as Schwann cell precursors (Adameyko et al., 2012), olfactory ensheathing glia (Barraud et al., 2010) or from multipotent cells in the dura that also are of a neural crest origin (Gagan et al., 2007). Classical lineage tracing and analysis of the temporal distribution of melanocytes in the meninges can be used to establish this.
The role of meningeal melanocytes remains unknown. The anatomical locations of these melanocytes in areas susceptible to infection such as the olfactory bulb via the olfactory epithelium, might suggest a possible role for these cells in the immune response. This is consistent with previous observations that melanocytes produce proinflammatory cytokines such as IL-8 (Miniati et al., 2014) and may modulate inflammation by NO production (reviewed in Tsatmali et al., 2002). NO also plays a key role in headaches, such as migraine, through its vasodilation effect on the meningeal vasculature. In that light it is interesting to note that meningeal pigment cells have recently been linked with aneurysm formation (Schulter et al., 2014) suggesting that these cells may play a role in the vasculature.
Diseases with known connections with melanocytes can roughly be grouped into neoplastic diseases and diseases of possible autoimmune etiology such as Vogt-Koyanagi-Harada syndrome (Greco et al., 2013). The diseases that most clearly involve meningeal melanocytes are the primary meningeal melanocytic neoplasms and their variants. Primary meningeal melanocytic neoplasms are rare potentially lethal forms of cancer in humans. According to the WHO guidelines for classification of tumors of the central nervous system (Louis et al., 2007) they are classified as diffuse meningeal melanocytosis, meningeal melanocytoma, malignant meningeal melanoma and meningeal melanomatosis. The most common is meningeal melanocytoma, occurring in 1 in 10 million individuals (Liubinas et al., 2010). Meningeal melanocytoma is a generally benign neoplasm, which can undergo malignant transformation (Brunsvig et al., 2011; Wang et al., 2011). A common site for a melanocytoma is in Meckels cave (Botticelli et al., 1983; Chen et al., 1997; Leonardi et al., 1998; Kurita et al., 2000; Tregnago et al., 2015) which contains the trigeminal ganglion and lies adjacent to the internal carotid artery (Arslan et al., 2012). This corresponds to the pterygopalatine artery in our observations as it arises from the internal carotid in rodents. This suggests that these neoplasms might originate in resident melanocytes in the meninges. Pedersen et al. (2013) created a mouse model for meningeal melanoma by expressing oncogenic NRASG12D in melanocytes of developing embryos. Although this mutation did not induce cutaneous melanoma, it resulted in early-onset primary melanoma of the CNS. The disease was most commonly located in the leptomeninges surrounding the anterior portion of the CNS, most notably around the olfactory bulb. Based on our results it is likely that these melanomas arise from pre-existing melanocytes in these areas.
Funding
This work was supported by grant 120405021 from the Icelandic Research Fund to ES and PHP. ES and LL were supported by PHC JULES VERNE 2014 (31891VM). LL and FG were supported by Ligue Nationale Contre le Cancer (Equipe labellisée), Cancéropole Ile-de-France, INCa and Pair Mélanome. IH and GR were supported by the French National Research Agency through the “Investments for the Future” program (France-BioImaging, ANR-10-INSB-04). LL, FG, IH and GR acknowledge the PICT-IBiSA, member of the France-BioImaging national research infrastructure, supported by the CelTisPhyBio Labex (N ANR-10-LBX-0038) part of the IDEX PSL (N ANR-10-IDEX-0001-02 PSL).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We thank Olof Sigurdardottir at The Institute for Experimental Pathology, Keldur, Sigrun Kristjansdottir and Sigurros Jonasdottir at the Department of Pathology, Landspitali University Hospital for assistance with paraffin sectioning of samples and with histochemical staining and Johann Arnfinnsson for his help with the preparation of the EM samples.
References
Adameyko, I., Lallemend, F., Furlan, A., Zinin, N., Aranda, S., Kitambi, S. S., et al. (2012). Sox2 and Mitf cross-regulatory interactions consolidate progenitor and melanocyte lineages in the cranial neural crest. Development 139, 397–410. doi: 10.1242/dev.065581
Arslan, M., Deda, H., Avci, E., Elhan, A., Tekdemir, I., Tubbs, R. S., et al. (2012). Anatomy of Meckels cave and the trigeminal ganglion: anatomical landmarks for a safer approach to them. Turk. Neurosurg. 22, 317–323. doi: 10.5137/1019-5149.JTN.5213-11.1
Baker, C. V., Bronner-Fraser, M., Le Douarin, N. M., and Teillet, M. A. (1997). Early- and late-migrating cranial neural crest cell populations have equivalent developmental potential in vivo. Development 124, 3077–3087.
Barden, H., and Levine, S. (1983). Histochemical observations on rodent brain melanin. Brain Res. Bull. 10, 847–851. doi: 10.1016/0361-9230(83)90218-6
Barraud, P., Seferiadis, A. A., Tyson, L. D., Zwart, M. F., Szabo-Rogers, H. L., Ruhrberg, C., et al. (2010). Neural crest origin of olfactory ensheathing glia. Proc. Natl. Acad. Sci. U S A 107, 21040–21045. doi: 10.1073/pnas.1012248107
Baxter, L. L., and Pavan, W. J. (2003). Pmel17 expression is Mitf-dependent and reveals cranial melanoblast migration during murine development. Gene Expr. Patterns 3, 703–707. doi: 10.1016/s0925-4773(03)00180-1
Botticelli, A. R., Villani, M., Angiari, P., and Peserico, L. (1983). Meningeal melanocytoma of Meckel’s cave associated with ipsilateral Ota’s nevus. Cancer 51, 2304–2310. doi: 10.1002/1097-0142(19830615)51:122304::aid-cncr28205112233.0.co;2-u
Brunsvig, K. L., Zenobi, M., Rilliet, B., El Hassani, Y., de Haller, R., Ansari, M., et al. (2011). Primary leptomeningeal melanocytosis in a 10-year-old girl: a challenging diagnosis with a poor prognosis. J. Child Neurol. 26, 1444–1448. doi: 10.1177/0883073811409749
Chen, C. J., Hsu, Y. I., Ho, Y. S., Hsu, Y. H., Wang, L. J., and Wong, Y. C. (1997). Intracranial meningeal melanocytoma: CT and MRI. Neuroradiology 39, 811–814. doi: 10.1007/s002340050510
Chomczynski, P., and Sacchi, N. (1987). Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162, 156–159. doi: 10.1016/0003-2697(87)90021-2
Colombo, S., Berlin, I., Delmas, V., and Larue, L. (2011). “Classical and nonclassical melanocytes in vertebrates,” in Melanins and Melanosomes: Biosynthesis, Biogenesis, Physiological, and Pathological Functions, eds J. Borovanský and P. A. Riley (Weinheim: Wiley-VCH Verlag GmbH and Co. KGaA), 21–61. doi: 10.1002/9783527636150.ch2
Eckhart, L., Bach, J., Ban, J., and Tschachler, E. (2000). Melanin binds reversibly to thermostable DNA polymerase and inhibits its activity. Biochem. Biophys. Res. Commun. 271, 726–730. doi: 10.1006/bbrc.2000.2716
Fetissov, S. O., Barcza, M. A., Meguid, M. M., and Oler, A. (1999). Hypophysial and meningeal melanocytes in the Zucker rat. Pigment Cell Res. 12, 323–330. doi: 10.1111/j.1600-0749.1999.tb00766.x
Gagan, J. R., Tholpady, S. S., and Ogle, R. C. (2007). Cellular dynamics and tissue interactions of the dura mater during head development. Birth Defects Res. C Embryo Today 81, 297–304. doi: 10.1002/bdrc.20104
Goldgeier, M. H., Klein, L. E., Klein-Angerer, S., Moellmann, G., and Nordlund, J. J. (1984). The distribution of melanocytes in the leptomeninges of the human brain. J. Invest. Dermatol. 82, 235–238. doi: 10.1111/1523-1747.ep12260111
Greco, A., Fusconi, M., Gallo, A., Turchetta, R., Marinelli, C., Macri, G. F., et al. (2013). Vogt-Koyanagi-Harada syndrome. Autoimmun. Rev. 12, 1033–1038. doi: 10.1016/j.autrev.2013.01.004
Grimelius, L., Su, H., and Hacker, G. (1994). “The use of silver stains in the identification of neuroendocrine cell types,” in Modern Methods in Analytical Morphology, eds J. Gu and G. Hacker (New York: Springer), 1–8.
Hodgkinson, C. A., Moore, K. J., Nakayama, A., Steingrimsson, E., Copeland, N. G., Jenkins, N. A., et al. (1993). Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 74, 395–404. doi: 10.1016/0092-8674(93)90429-t
Kurita, H., Segawa, H., Shin, M., Ueki, K., Ichi, S., Sasaki, T., et al. (2000). Radiosurgery of meningeal melanocytoma. J. Neurooncol. 46, 57–61. doi: 10.1023/A:1006335616839
Leonardi, M. A., Lumenta, C. B., Stolzle, A., and Muller-Hocker, J. (1998). Unusual clinical presentation of a meningeal melanocytoma with seizures: case report and review of the literature. Acta Neurochir. (Wien) 140, 621–628. doi: 10.1007/s007010050151
Lewis, M. G. (1969). Melanoma and pigmentation of the leptomeninges in Ugandan Africans. J. Clin. Pathol. 22, 183–186. doi: 10.1136/jcp.22.2.183
Liubinas, S. V., Maartens, N., and Drummond, K. J. (2010). Primary melanocytic neoplasms of the central nervous system. J. Clin. Neurosci. 17, 1227–1232. doi: 10.1016/j.jocn.2010.01.017
Louis, D. N., Ohgaki, H., Wiestler, O. D., Cavenee, W. K., Burger, P. C., Jouvet, A., et al. (2007). The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol. 114, 97–109. doi: 10.1007/s00401-007-0243-4
Lugassy, C., Zadran, S., Bentolila, L. A., Wadehra, M., Prakash, R., Carmichael, S. T., et al. (2014). Angiotropism, pericytic mimicry and extravascular migratory metastasis in melanoma: an alternative to intravascular cancer dissemination. Cancer Microenviron. 7, 139–152. doi: 10.1007/s12307-014-0156-4
Markert, C. L., and Silvers, W. K. (1956). The effects of genotype and cell environment on melanoblast differentiation in the house mouse. Genetics 41, 429–450.
Miniati, A., Weng, Z., Zhang, B., Therianou, A., Vasiadi, M., Nicolaidou, E., et al. (2014). Stimulated human melanocytes express and release interleukin-8, which is inhibited by luteolin: relevance to early vitiligo. Clin. Exp. Dermatol. 39, 54–57. doi: 10.1111/ced.12164
Morse, D. E., and Cova, J. L. (1984). Pigmented cells in the leptomeninges of the cat. Anat. Rec. 210, 125–132. doi: 10.1002/ar.1092100115
Ni, C., Zhang, D., Beyer, L. A., Halsey, K. E., Fukui, H., Raphael, Y., et al. (2013). Hearing dysfunction in heterozygous Mitf(Mi-wh) /+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome. Pigment Cell Melanoma Res. 26, 78–87. doi: 10.1111/pcmr.12030
Pedersen, M., Kusters-Vandevelde, H. V., Viros, A., Groenen, P. J., Sanchez-Laorden, B., Gilhuis, J. H., et al. (2013). Primary melanoma of the CNS in children is driven by congenital expression of oncogenic NRAS in melanocytes. Cancer Discov. 3, 458–469. doi: 10.1158/2159-8290.cd-12-0464
Schulter, G., Leber, K., Kronawetter, E., Rubenbauer, V. R., Konstantiniuk, P., and Papousek, I. (2014). Body pigmentation as a risk factor for the formation of intracranial aneurysms. Biomed Res. Int. 2014:301631. doi: 10.1155/2014/301631
Steingrimsson, E., Copeland, N. G., and Jenkins, N. A. (2004). Melanocytes and the microphthalmia transcription factor network. Annu. Rev. Genet. 38, 365–411. doi: 10.1146/annurev.genet.38.072902.092717
Tregnago, A. C., Furlan, M. V., Bezerra, S. M., Gc, M. P., Mendes, G. G., Henklain, J. V., et al. (2015). Orbital melanocytoma completely resected with conservative surgery in association with ipsilateral nevus of Ota: report of a case and review of the literature. Head Neck 37, E49–E55. doi: 10.1002/hed.23828
Tsatmali, M., Ancans, J., and Thody, A. J. (2002). Melanocyte function and its control by melanocortin peptides. J. Histochem. Cytochem. 50, 125–133. doi: 10.1177/002215540205000201
Wang, F., Qiao, G., Lou, X., Song, X., and Chen, W. (2011). Malignant transformation of intracranial meningeal melanocytoma. Case report and review of the literature. Neuropathology 31, 414–420. doi: 10.1111/j.1440-1789.2010.01160.x
Keywords: melanocytes, meninges, mouse, Mitf, meningeal melanoma
Citation: Gudjohnsen SAH, Atacho DAM, Gesbert F, Raposo G, Hurbain I, Larue L, Steingrimsson E and Petersen PH (2015) Meningeal Melanocytes in the Mouse: Distribution and Dependence on Mitf. Front. Neuroanat. 9:149. doi: 10.3389/fnana.2015.00149
Received: 18 June 2015; Accepted: 06 November 2015;
Published: 25 November 2015.
Edited by:
Luis Puelles, Universidad de Murcia, SpainReviewed by:
Nobuaki Tamamaki, Kumamoto University, JapanSalvador Martinez, University Miguel Hernandez, Spain
Copyright © 2015 Gudjohnsen, Atacho, Gesbert, Raposo, Hurbain, Larue, Steingrimsson and Petersen. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution and reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Eirikur Steingrimsson, eirikurs@hi.is