Identification of the fate and regenerative mechanism of zebrafish melanocyte progenitor cells and melanocytes after laser‐induced pigment ablation

Background and Objectives Lasers are known to be the most effective treatment modality for pigmentary skin diseases. However, melanocytes and melanin pigment often recur or leave post‐inflammatory hyperpigmentation after the laser procedure. Studies have reported on the role of progenitor cells in p...

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Veröffentlicht in:Lasers in surgery and medicine 2022-02, Vol.54 (2), p.281-288
Hauptverfasser: Park, Ji Hyun, Koun, Soonil, Kim, Ko Eun, Kim, Il‐Hwan
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creator Park, Ji Hyun
Koun, Soonil
Kim, Ko Eun
Kim, Il‐Hwan
description Background and Objectives Lasers are known to be the most effective treatment modality for pigmentary skin diseases. However, melanocytes and melanin pigment often recur or leave post‐inflammatory hyperpigmentation after the laser procedure. Studies have reported on the role of progenitor cells in pigment cell regeneration, which can be constantly replenished through mitosis. However, the response of unpigmented melanocyte progenitor cells to laser treatment is poorly understood. In this study, we used adult zebrafish skin as the melanocyte regenerative system and examined the response of melanocyte progenitor cells to laser photothermolysis. Materials and Methods The two groups of adult zebrafish were irradiated with 1064 nm wavelength laser system of Q‐switched neodymium:yttrium–aluminum–garnet (Nd:YAG) laser with 0.3 or 0.7 J·cm−2. We compared the regeneration of pigment at different energy levels by measuring new melanocyte counts and pigment area. We traced and quantitatively compared the melanocyte lineage cells by immunohistochemical staining using specific markers such as sox10, mitfa, and dct during the regeneration process. Three repetitive laser ablations were also held to test the postinflammatory hyperpigmentation. Results After the laser ablation of melanocytes, most of the new melanocytes appeared between Days 5 and 10. In high‐energy irradiation of 0.7 J·cm−2, the unpigmented mitfa‐expressing cells showed significant decrease (p 
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However, melanocytes and melanin pigment often recur or leave post‐inflammatory hyperpigmentation after the laser procedure. Studies have reported on the role of progenitor cells in pigment cell regeneration, which can be constantly replenished through mitosis. However, the response of unpigmented melanocyte progenitor cells to laser treatment is poorly understood. In this study, we used adult zebrafish skin as the melanocyte regenerative system and examined the response of melanocyte progenitor cells to laser photothermolysis. Materials and Methods The two groups of adult zebrafish were irradiated with 1064 nm wavelength laser system of Q‐switched neodymium:yttrium–aluminum–garnet (Nd:YAG) laser with 0.3 or 0.7 J·cm−2. We compared the regeneration of pigment at different energy levels by measuring new melanocyte counts and pigment area. We traced and quantitatively compared the melanocyte lineage cells by immunohistochemical staining using specific markers such as sox10, mitfa, and dct during the regeneration process. Three repetitive laser ablations were also held to test the postinflammatory hyperpigmentation. Results After the laser ablation of melanocytes, most of the new melanocytes appeared between Days 5 and 10. In high‐energy irradiation of 0.7 J·cm−2, the unpigmented mitfa‐expressing cells showed significant decrease (p &lt; 0.05) and showed delay in the differentiation process of melanocyte lineage cells. After repeated laser irradiation, hyperpigmentation did not appear and the final recovery ratio of the pigmented area was 87.5% and 75.3% at the 0.3 and 0.7 J·cm−2 energy levels, respectively. Conclusion We suggest that laser treatment overcoming the recurrence should be planned based on the adequate energy level targeting the melanocyte progenitor cells. High‐energy irradiation may induce apoptosis of progenitor cells and delay their process of differentiation. Short‐term repetitive sessions of laser therapy can reduce the pigmentation in the long‐term observation.</description><identifier>ISSN: 0196-8092</identifier><identifier>EISSN: 1096-9101</identifier><identifier>DOI: 10.1002/lsm.23458</identifier><identifier>PMID: 34298588</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Ablation ; Aluminum ; Animals ; Apoptosis ; Cell differentiation ; Cells (biology) ; Danio rerio ; Differentiation ; Energy ; Hyperpigmentation ; Hyperpigmentation - etiology ; Hyperpigmentation - surgery ; Inflammation ; Irradiation ; laser ; Laser ablation ; Lasers ; Lasers, Solid-State - therapeutic use ; Low-Level Light Therapy ; Melanin ; melanocyte ; Melanocytes ; Mitosis ; Neodymium ; Neodymium lasers ; Pigmentation ; postinflammatory hyperpigmentation ; progenitor cell ; Progenitor cells ; Regeneration ; Skin diseases ; Sox10 protein ; Stem Cells ; YAG lasers ; Yttrium ; Zebrafish</subject><ispartof>Lasers in surgery and medicine, 2022-02, Vol.54 (2), p.281-288</ispartof><rights>2021 Wiley Periodicals LLC</rights><rights>2021 Wiley Periodicals LLC.</rights><rights>2022 Wiley Periodicals LLC</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-4ed890cc1dbd402ec6ee8ffaace7fd5eeee997a6ca0c05393ec80e2dfde8094e3</citedby><cites>FETCH-LOGICAL-c3538-4ed890cc1dbd402ec6ee8ffaace7fd5eeee997a6ca0c05393ec80e2dfde8094e3</cites><orcidid>0000-0002-4141-204X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Flsm.23458$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Flsm.23458$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34298588$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Ji Hyun</creatorcontrib><creatorcontrib>Koun, Soonil</creatorcontrib><creatorcontrib>Kim, Ko Eun</creatorcontrib><creatorcontrib>Kim, Il‐Hwan</creatorcontrib><title>Identification of the fate and regenerative mechanism of zebrafish melanocyte progenitor cells and melanocytes after laser‐induced pigment ablation</title><title>Lasers in surgery and medicine</title><addtitle>Lasers Surg Med</addtitle><description>Background and Objectives Lasers are known to be the most effective treatment modality for pigmentary skin diseases. However, melanocytes and melanin pigment often recur or leave post‐inflammatory hyperpigmentation after the laser procedure. Studies have reported on the role of progenitor cells in pigment cell regeneration, which can be constantly replenished through mitosis. However, the response of unpigmented melanocyte progenitor cells to laser treatment is poorly understood. In this study, we used adult zebrafish skin as the melanocyte regenerative system and examined the response of melanocyte progenitor cells to laser photothermolysis. Materials and Methods The two groups of adult zebrafish were irradiated with 1064 nm wavelength laser system of Q‐switched neodymium:yttrium–aluminum–garnet (Nd:YAG) laser with 0.3 or 0.7 J·cm−2. We compared the regeneration of pigment at different energy levels by measuring new melanocyte counts and pigment area. We traced and quantitatively compared the melanocyte lineage cells by immunohistochemical staining using specific markers such as sox10, mitfa, and dct during the regeneration process. Three repetitive laser ablations were also held to test the postinflammatory hyperpigmentation. Results After the laser ablation of melanocytes, most of the new melanocytes appeared between Days 5 and 10. In high‐energy irradiation of 0.7 J·cm−2, the unpigmented mitfa‐expressing cells showed significant decrease (p &lt; 0.05) and showed delay in the differentiation process of melanocyte lineage cells. After repeated laser irradiation, hyperpigmentation did not appear and the final recovery ratio of the pigmented area was 87.5% and 75.3% at the 0.3 and 0.7 J·cm−2 energy levels, respectively. Conclusion We suggest that laser treatment overcoming the recurrence should be planned based on the adequate energy level targeting the melanocyte progenitor cells. High‐energy irradiation may induce apoptosis of progenitor cells and delay their process of differentiation. Short‐term repetitive sessions of laser therapy can reduce the pigmentation in the long‐term observation.</description><subject>Ablation</subject><subject>Aluminum</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Cell differentiation</subject><subject>Cells (biology)</subject><subject>Danio rerio</subject><subject>Differentiation</subject><subject>Energy</subject><subject>Hyperpigmentation</subject><subject>Hyperpigmentation - etiology</subject><subject>Hyperpigmentation - surgery</subject><subject>Inflammation</subject><subject>Irradiation</subject><subject>laser</subject><subject>Laser ablation</subject><subject>Lasers</subject><subject>Lasers, Solid-State - therapeutic use</subject><subject>Low-Level Light Therapy</subject><subject>Melanin</subject><subject>melanocyte</subject><subject>Melanocytes</subject><subject>Mitosis</subject><subject>Neodymium</subject><subject>Neodymium lasers</subject><subject>Pigmentation</subject><subject>postinflammatory hyperpigmentation</subject><subject>progenitor cell</subject><subject>Progenitor cells</subject><subject>Regeneration</subject><subject>Skin diseases</subject><subject>Sox10 protein</subject><subject>Stem Cells</subject><subject>YAG lasers</subject><subject>Yttrium</subject><subject>Zebrafish</subject><issn>0196-8092</issn><issn>1096-9101</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kcFuEzEQhi0EoqFw4AWQJS5wSDu214l9rCpKKwVxaDlbjj1uXO16g70LSk99hF54QZ4EJ2lBqsRcPPZ8_vVrfkLeMjhiAPy4Ld0RF41Uz8iEgZ5NNQP2nEyA1V6B5gfkVSk3ACA4zF-SA9FwraRSE_LrwmMaYojODrFPtA90WCENdkBqk6cZrzFhrsMfSDt0K5ti6bbYLS6zDbGs6nNrU-829cs695WPQ5-pw7YtO41_83oPA2ba2oL59919TH506Ok6XnfVBrXLdmfjNXkRbFvwzcN5SL6dfbo6PZ8uvn6-OD1ZTJ2QQk0b9EqDc8wvfQMc3QxRhWCtw3nwEmtpPbczZ8GBFFqgU4DcB491Kw2KQ_Jhr1t9fx-xDKaLZWvcJuzHYriUkkEjmaro-yfoTT_mVN0ZPhOgZV2nrNTHPeVyX0rGYNY5djZvDAOzzcrUrMwuq8q-e1Aclx36v-RjOBU43gM_Y4ub_yuZxeWXveQfF-Sj4w</recordid><startdate>202202</startdate><enddate>202202</enddate><creator>Park, Ji Hyun</creator><creator>Koun, Soonil</creator><creator>Kim, Ko Eun</creator><creator>Kim, Il‐Hwan</creator><general>Wiley Subscription Services, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4141-204X</orcidid></search><sort><creationdate>202202</creationdate><title>Identification of the fate and regenerative mechanism of zebrafish melanocyte progenitor cells and melanocytes after laser‐induced pigment ablation</title><author>Park, Ji Hyun ; Koun, Soonil ; Kim, Ko Eun ; Kim, Il‐Hwan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-4ed890cc1dbd402ec6ee8ffaace7fd5eeee997a6ca0c05393ec80e2dfde8094e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Ablation</topic><topic>Aluminum</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Cell differentiation</topic><topic>Cells (biology)</topic><topic>Danio rerio</topic><topic>Differentiation</topic><topic>Energy</topic><topic>Hyperpigmentation</topic><topic>Hyperpigmentation - etiology</topic><topic>Hyperpigmentation - surgery</topic><topic>Inflammation</topic><topic>Irradiation</topic><topic>laser</topic><topic>Laser ablation</topic><topic>Lasers</topic><topic>Lasers, Solid-State - therapeutic use</topic><topic>Low-Level Light Therapy</topic><topic>Melanin</topic><topic>melanocyte</topic><topic>Melanocytes</topic><topic>Mitosis</topic><topic>Neodymium</topic><topic>Neodymium lasers</topic><topic>Pigmentation</topic><topic>postinflammatory hyperpigmentation</topic><topic>progenitor cell</topic><topic>Progenitor cells</topic><topic>Regeneration</topic><topic>Skin diseases</topic><topic>Sox10 protein</topic><topic>Stem Cells</topic><topic>YAG lasers</topic><topic>Yttrium</topic><topic>Zebrafish</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Ji Hyun</creatorcontrib><creatorcontrib>Koun, Soonil</creatorcontrib><creatorcontrib>Kim, Ko Eun</creatorcontrib><creatorcontrib>Kim, Il‐Hwan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Lasers in surgery and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Ji Hyun</au><au>Koun, Soonil</au><au>Kim, Ko Eun</au><au>Kim, Il‐Hwan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of the fate and regenerative mechanism of zebrafish melanocyte progenitor cells and melanocytes after laser‐induced pigment ablation</atitle><jtitle>Lasers in surgery and medicine</jtitle><addtitle>Lasers Surg Med</addtitle><date>2022-02</date><risdate>2022</risdate><volume>54</volume><issue>2</issue><spage>281</spage><epage>288</epage><pages>281-288</pages><issn>0196-8092</issn><eissn>1096-9101</eissn><abstract>Background and Objectives Lasers are known to be the most effective treatment modality for pigmentary skin diseases. However, melanocytes and melanin pigment often recur or leave post‐inflammatory hyperpigmentation after the laser procedure. Studies have reported on the role of progenitor cells in pigment cell regeneration, which can be constantly replenished through mitosis. However, the response of unpigmented melanocyte progenitor cells to laser treatment is poorly understood. In this study, we used adult zebrafish skin as the melanocyte regenerative system and examined the response of melanocyte progenitor cells to laser photothermolysis. Materials and Methods The two groups of adult zebrafish were irradiated with 1064 nm wavelength laser system of Q‐switched neodymium:yttrium–aluminum–garnet (Nd:YAG) laser with 0.3 or 0.7 J·cm−2. We compared the regeneration of pigment at different energy levels by measuring new melanocyte counts and pigment area. We traced and quantitatively compared the melanocyte lineage cells by immunohistochemical staining using specific markers such as sox10, mitfa, and dct during the regeneration process. Three repetitive laser ablations were also held to test the postinflammatory hyperpigmentation. Results After the laser ablation of melanocytes, most of the new melanocytes appeared between Days 5 and 10. In high‐energy irradiation of 0.7 J·cm−2, the unpigmented mitfa‐expressing cells showed significant decrease (p &lt; 0.05) and showed delay in the differentiation process of melanocyte lineage cells. After repeated laser irradiation, hyperpigmentation did not appear and the final recovery ratio of the pigmented area was 87.5% and 75.3% at the 0.3 and 0.7 J·cm−2 energy levels, respectively. Conclusion We suggest that laser treatment overcoming the recurrence should be planned based on the adequate energy level targeting the melanocyte progenitor cells. High‐energy irradiation may induce apoptosis of progenitor cells and delay their process of differentiation. Short‐term repetitive sessions of laser therapy can reduce the pigmentation in the long‐term observation.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>34298588</pmid><doi>10.1002/lsm.23458</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-4141-204X</orcidid></addata></record>
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subjects Ablation
Aluminum
Animals
Apoptosis
Cell differentiation
Cells (biology)
Danio rerio
Differentiation
Energy
Hyperpigmentation
Hyperpigmentation - etiology
Hyperpigmentation - surgery
Inflammation
Irradiation
laser
Laser ablation
Lasers
Lasers, Solid-State - therapeutic use
Low-Level Light Therapy
Melanin
melanocyte
Melanocytes
Mitosis
Neodymium
Neodymium lasers
Pigmentation
postinflammatory hyperpigmentation
progenitor cell
Progenitor cells
Regeneration
Skin diseases
Sox10 protein
Stem Cells
YAG lasers
Yttrium
Zebrafish
title Identification of the fate and regenerative mechanism of zebrafish melanocyte progenitor cells and melanocytes after laser‐induced pigment ablation
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