Human melanocytes form a PAX3-expressing melanocyte cluster on Matrigel by the cell migration process

•Normal human melanocytes (NHMs) migrated to form cell clusters on Matrigel.•The melanin synthesis is significantly decreased in melanocyte clusters on Matrigel.•The PAX3 level of melanocyte clusters on Matrigel is upregulated.•The expression profile of PAX3, SOX10, and MITF in the cluster is simila...

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Veröffentlicht in:Journal of dermatological science 2014-10, Vol.76 (1), p.60-66
Hauptverfasser: Choi, Hyunjung, Jin, Sun Hee, Han, Mi Hwa, Lee, Jinyoung, Ahn, Seyeon, Seong, Minjeong, Choi, Hyun, Han, Jiyeon, Cho, Eun-Gyung, Lee, Tae Ryong, Noh, Minsoo
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container_issue 1
container_start_page 60
container_title Journal of dermatological science
container_volume 76
creator Choi, Hyunjung
Jin, Sun Hee
Han, Mi Hwa
Lee, Jinyoung
Ahn, Seyeon
Seong, Minjeong
Choi, Hyun
Han, Jiyeon
Cho, Eun-Gyung
Lee, Tae Ryong
Noh, Minsoo
description •Normal human melanocytes (NHMs) migrated to form cell clusters on Matrigel.•The melanin synthesis is significantly decreased in melanocyte clusters on Matrigel.•The PAX3 level of melanocyte clusters on Matrigel is upregulated.•The expression profile of PAX3, SOX10, and MITF in the cluster is similar to that of melanoblasts. The interactions between human epidermal melanocytes and their cellular microenvironment are important in the regulation of human melanocyte functions or in their malignant transformation into melanoma. Although the basement membrane extracellular matrix (BM-ECM) is one of major melanocyte microenvironments, the effects of BM-ECM on the human melanocyte functions are not fully explained at a molecular level. This study was aimed to characterize the molecular and cellular interactions between normal human melanocytes (NHMs) and BM-ECM. We investigated cell culture models of normal human melanocytes or melanoma cells on three-dimensional (3D) Matrigel to understand the roles of the basement membrane microenvironment in human melanocyte functions. Melanogenesis and melanobast biomarker expression in both primary human melanocytes and melanoma cells on 3D Matrigel were evaluated. We found that NHMs migrated and formed reversible paired box 3 (PAX3) expressing cell clusters on three-dimensional (3D) Matrigel. The melanogenesis was significantly decreased in the PAX3 expressing cell cluster. The expression profile of PAX3, SOX10, and MITF in the melanocyte cluster on 3D Matrigel was similar to that of melanoblasts. Interestingly, PAX3 and SOX10 showed an inverse expression profile in NHMs, whereas the inverse expression pattern of PAX3 and SOX10 was disrupted in melanoma MNT1 and WM266-4 cells. The human melanocyte culture on 3D Matrigel provides an alternative model system to study functions of human melanoblasts. In addition, this system will contribute to the elucidation of PAX3-related tumorigenic mechanisms to understand human melanoma.
doi_str_mv 10.1016/j.jdermsci.2014.07.006
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The interactions between human epidermal melanocytes and their cellular microenvironment are important in the regulation of human melanocyte functions or in their malignant transformation into melanoma. Although the basement membrane extracellular matrix (BM-ECM) is one of major melanocyte microenvironments, the effects of BM-ECM on the human melanocyte functions are not fully explained at a molecular level. This study was aimed to characterize the molecular and cellular interactions between normal human melanocytes (NHMs) and BM-ECM. We investigated cell culture models of normal human melanocytes or melanoma cells on three-dimensional (3D) Matrigel to understand the roles of the basement membrane microenvironment in human melanocyte functions. Melanogenesis and melanobast biomarker expression in both primary human melanocytes and melanoma cells on 3D Matrigel were evaluated. We found that NHMs migrated and formed reversible paired box 3 (PAX3) expressing cell clusters on three-dimensional (3D) Matrigel. The melanogenesis was significantly decreased in the PAX3 expressing cell cluster. The expression profile of PAX3, SOX10, and MITF in the melanocyte cluster on 3D Matrigel was similar to that of melanoblasts. Interestingly, PAX3 and SOX10 showed an inverse expression profile in NHMs, whereas the inverse expression pattern of PAX3 and SOX10 was disrupted in melanoma MNT1 and WM266-4 cells. The human melanocyte culture on 3D Matrigel provides an alternative model system to study functions of human melanoblasts. 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The interactions between human epidermal melanocytes and their cellular microenvironment are important in the regulation of human melanocyte functions or in their malignant transformation into melanoma. Although the basement membrane extracellular matrix (BM-ECM) is one of major melanocyte microenvironments, the effects of BM-ECM on the human melanocyte functions are not fully explained at a molecular level. This study was aimed to characterize the molecular and cellular interactions between normal human melanocytes (NHMs) and BM-ECM. We investigated cell culture models of normal human melanocytes or melanoma cells on three-dimensional (3D) Matrigel to understand the roles of the basement membrane microenvironment in human melanocyte functions. Melanogenesis and melanobast biomarker expression in both primary human melanocytes and melanoma cells on 3D Matrigel were evaluated. 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The interactions between human epidermal melanocytes and their cellular microenvironment are important in the regulation of human melanocyte functions or in their malignant transformation into melanoma. Although the basement membrane extracellular matrix (BM-ECM) is one of major melanocyte microenvironments, the effects of BM-ECM on the human melanocyte functions are not fully explained at a molecular level. This study was aimed to characterize the molecular and cellular interactions between normal human melanocytes (NHMs) and BM-ECM. We investigated cell culture models of normal human melanocytes or melanoma cells on three-dimensional (3D) Matrigel to understand the roles of the basement membrane microenvironment in human melanocyte functions. Melanogenesis and melanobast biomarker expression in both primary human melanocytes and melanoma cells on 3D Matrigel were evaluated. We found that NHMs migrated and formed reversible paired box 3 (PAX3) expressing cell clusters on three-dimensional (3D) Matrigel. The melanogenesis was significantly decreased in the PAX3 expressing cell cluster. The expression profile of PAX3, SOX10, and MITF in the melanocyte cluster on 3D Matrigel was similar to that of melanoblasts. Interestingly, PAX3 and SOX10 showed an inverse expression profile in NHMs, whereas the inverse expression pattern of PAX3 and SOX10 was disrupted in melanoma MNT1 and WM266-4 cells. The human melanocyte culture on 3D Matrigel provides an alternative model system to study functions of human melanoblasts. In addition, this system will contribute to the elucidation of PAX3-related tumorigenic mechanisms to understand human melanoma.</abstract><cop>Netherlands</cop><pub>Elsevier Ireland Ltd</pub><pmid>25128984</pmid><doi>10.1016/j.jdermsci.2014.07.006</doi><tpages>7</tpages></addata></record>
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subjects Basement Membrane - metabolism
Cell Line, Tumor
Cell Movement
Collagen - chemistry
Dermatology
Drug Combinations
Extracellular Matrix - metabolism
Gene Expression Profiling
Human melanocytes
Humans
Laminin - chemistry
Matrigel
Melanins - chemistry
Melanoblast
Melanocyte cluster
Melanocytes - cytology
Melanocytes - metabolism
Melanoma
Melanoma - metabolism
Microphthalmia-Associated Transcription Factor - metabolism
Paired Box Transcription Factors - metabolism
PAX3
PAX3 Transcription Factor
Pigmentation
Proteoglycans - chemistry
SOXE Transcription Factors - metabolism
Up-Regulation
title Human melanocytes form a PAX3-expressing melanocyte cluster on Matrigel by the cell migration process
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