Real-time visualization of melanin granules in normal human skin using combined multiphoton and reflectance confocal microscopy

被引:5
作者
Majdzadeh, Ali [1 ,2 ,3 ]
Lee, Anthony M. D. [1 ,2 ]
Wang, Hequn [1 ]
Lui, Harvey [1 ,4 ,5 ]
McLean, David I. [4 ,5 ]
Crawford, Richard I. [4 ,5 ,6 ]
Zloty, David [3 ,4 ,5 ]
Zeng, Haishan [1 ,2 ,4 ,5 ,6 ]
机构
[1] British Columbia Canc Agcy, Integrat Oncol Dept, Imaging Unit, Res Ctr, Vancouver, BC V5Z 1L3, Canada
[2] Univ British Columbia, Dept Phys & Astron, Vancouver, BC V5Z 1M9, Canada
[3] Univ British Columbia, Fac Med, Vancouver, BC V5Z 1M9, Canada
[4] Univ British Columbia, Dept Dermatol & Skin Sci, Photomed Inst, Vancouver, BC V5Z 1M9, Canada
[5] Vancouver Coastal Hlth Res Inst, Vancouver, BC, Canada
[6] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V5Z 1M9, Canada
基金
加拿大健康研究院;
关键词
melanin granule; multiphoton microscopy; reflectance confocal microscopy; skin; IN-VIVO; LASER TOMOGRAPHY; EX-VIVO; DIAGNOSIS; MELASMA;
D O I
10.1111/phpp.12161
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundRecent advances in biomedical optics have enabled dermal and epidermal components to be visualized at subcellular resolution and assessed noninvasively. Multiphoton microscopy (MPM) and reflectance confocal microscopy (RCM) are noninvasive imaging modalities that have demonstrated promising results in imaging skin micromorphology, and which provide complementary information regarding skin components. This study assesses whether combined MPM/RCM can visualize intracellular and extracellular melanin granules in the epidermis and dermis of normal human skin. MethodsWe perform MPM and RCM imaging of in vivo and ex vivo skin in the infrared domain. The inherent three-dimensional optical sectioning capability of MPM/RCM is used to image high-contrast granular features across skin depths ranging from 50 to 90m. The optical images thus obtained were correlated with conventional histologic examination including melanin-specific staining of ex vivo specimens. ResultsMPM revealed highly fluorescent granular structures below the dermal-epidermal junction (DEJ) region. Histochemical staining also demonstrated melanin-containing granules that correlate well in size and location with the granular fluorescent structures observed in MPM. Furthermore, the MPM fluorescence excitation wavelength and RCM reflectance of cell culture-derived melanin were equivalent to those of the granules. ConclusionThis study suggests that MPM can noninvasively visualize and quantify subepidermal melanin in situ.
引用
收藏
页码:141 / 148
页数:8
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