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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This paper reports that the addition of Y-27632 to TIVA medium can significantly increase the yield of melanocytes from adult skin tissues.

Abstract

The isolation and culture of primary melanocytes from skin tissues is very important for biological research and has been widely used for clinical applications. Isolating primary melanocytes from skin tissues by the conventional method usually takes about 3 to 4 weeks to passage sufficiently. More importantly, the tissues used are usually newborn foreskins and it is still a challenge to efficiently isolate primary melanocytes from adult tissues. We recently developed a new isolation method for melanocytes that adds Y-27632, a Rho kinase inhibitor, to the initial culture medium for 48 h. Compared with the conventional protocol, this new method dramatically increases the yield of melanocytes and shortens the time required to isolate melanocytes from foreskin tissues. We now describe this new method in more detail using adult epidermis to efficiently culture primary melanocytes. Importantly, we show that melanocytes obtained from adult tissues prepared by this new method can function normally. This new protocol will significantly benefit studies of pigmentation defects and melanomas using primary melanocytes prepared from easily accessed adult skin tissues.

Introduction

The goal of this study was to develop a simple and effective protocol to isolate melanocytes from the epidermis of adult skin for biological research and clinical applications. Melanocytes, which are located in the basal epidermis of the skin and in hair follicles, play an important role in pigmentation of the skin and hair by producing melanin1. The resulting skin pigmentation from epidermal melanocytes acts as an ultraviolet radiation filter that reduces/prevents DNA damage to underlying cells in the skin2. The abnormal proliferation of melanocytes in the skin is quite common, such as in the formation of benign n....

Protocol

The use of adult foreskin tissues in this protocol has been approved by the Human Research Ethics Committee (No.2015120401, date: May 12, 2015).

NOTE: Perform all the following procedures in a sterile environment to prevent contaminations of cells and cultures.

1. Preparations

  1. Gather fresh adult foreskin tissues from circumcision surgeries in 15 mL tubes containing 10 mL of phosphate buffer saline (PBS) and store in 4 °C.
    NOTE: Separate the t.......

Representative Results

Figure 1 shows a schematic diagram comparing the conventional and the new methods. The procedure for tissue preparation and digestion with the new method is the same as the procedure for the conventional method, the only difference being that the isolated cells are resuspended in 10 mL of TIVA medium in the presence of 10 µM Y-27632. Two days after seeding, replace the media with normal TIVA medium without Y-27632. The conventional method of isolating primary melanocytes from skin tissu.......

Discussion

The protocol described here was based on a recent publication16. Some attention should be paid to the following critical steps to achieve the best results with the new method. First, successful separation of the epidermis and the dermis is crucial. Cut the adult foreskin tissues into 3-4 mm wide strips using a scalpel blade to make the dispase work more thoroughly and easily to separate the epidermis from the dermis. Second, when separating those two layers, contamination of the dermis should be a.......

Acknowledgements

This work was supported by The National Key Research and Development Program of China (2017YFA0104604), The General Program of National Natural Science Foundation of China (81772093), Military Logistics Research Project (AWS17J005), the Key Program of Shandong Province Natural Science Foundation (ZR2019ZD36) and The Key Research and Development Program of Shandong Province (2019GSF108107) to X.W. Guangdong Basic and Applied Basic Research Foundation (2019A1515110833) and The Fundamental Research Funds of Shandong University (2019GN043) to J.M.

....

Materials

NameCompanyCatalog NumberComments
Alexa fluor-594 donkey anti-mouse IgGThermo Fisher ScientificA21203For Immunofluorescence
Alexa fluor-594 donkey anti-rabbit IgGThermo Fisher ScientificR37119For Immunofluorescence
Cell Culture DishEppendorf30702115For cell culture
Cell StrainerCorning incorporated431792Cell filtration
15 mL Centrifuge TubeKIRGEN171003For cell centrifuge
50 mL Centrifuge TubeKIRGEN171003For cell centrifuge
CO2 IncubatorThermo Scientific51026333For cell incubating
Constant Temperature ShakerShanghai Boxun150036For water bath
DAPIAbcamab104139For Immunofluorescence
DispaseGibco17105-041For melanocyte isolation
DMEMThermo ScientificC11995500Component of neutralization medium
Fetal Bovine SerumBiological Industries04-001-1AC5Component of neutralization medium
Fluorescence microscopeOlympus5E44316For Immunofluorescence
ForskolinMCEHY-15371Induce pigmentation
GlutamineThermo Fisher Scientific25030081melanocyte culture medium
Ham's F12Thermo Scientific11330032melanocyte culture medium
Inverted microscopeOlympus5C42258For cell microscopic observation
3-isobutyl-1-methyl xanthine (IBMX)Sigma17018melanocyte culture medium
mouse anti-human MITFAbcamab12039For Immunofluorescence
Na3VO4SigmaS6508melanocytes culture medium
N6,2'-O-dibutyryladeno-sine 3',5'-cyclic monophosphate (dbcAMP)SigmaD0627melanocyte culture medium
12-O-tetradecanoyl phorbol-13-acetate (TPA)Sigma79346melanocyte culture medium
Penicillin StreptomycinThermo Scientific15140-122Antibiotics
rabbit anti-human Ki-67Abcamab15580For Immunofluorescence
Phosphate buffered solutionSolarbio Life ScienceP1020-500Washing solution
Sorvall ST 16R CentrifugeThermo Scientific75004380Cell centrifugation
TC20TM automated cell counterBio-Rad1450102Automatic cell counting
0.05% TrypsinLife Technologies25300-062For melanocyte dissociation
Y-27632SigmaY0503For melanocyte isolation

References

  1. Costin, G. E., Hearing, V. J. Human skin pigmentation: melanocytes modulate skin color in response to stress. FASEB Journal. 21 (4), 976-994 (2007).
  2. Battyani, Z., Xerri, L., Hassoun, J., Bonerandi, J. J., Grob, J. J. Tyrosinase ge....

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