File:Melanocyte development cartoon.jpg - Revision history

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	====Copyright====		====Copyright====

	~~Articles published under~~ The Company of ~~Biologists’~~ Open Access ~~model will be made freely available online via The Company’s website immediately following publication, deposited in PMC for immediate release and can be~~ distributed under the terms of the Creative Commons Attribution (~~CC-BY) Licence (the terms of which are set out at~~ http://creativecommons.org/licenses/by/3.0~~/legalcode~~)~~. Authors retain ownership of the copyright for their article~~, ~~but undertake to allow anyone to download, reuse, reprint, modify, distribute~~, and~~/or copy articles, including for commercial purposes,~~ provided that:		© 2014. Published by The Company of Biologists Ltd This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

	~~(1)~~ the original ~~authorship~~ is properly ~~and fully~~ attributed ~~and the journal is attributed as the original place of publication with correct citation details given;~~

	~~(2) if an original work is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this is clearly indicated.~~

	~~No permission is required from the authors or the publishers under the CC-BY licence~~.

	[[Category:Neural Crest]]		[[Category:Neural Crest]]

Z8600021 at 11:18, 3 March 2015

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	No permission is required from the authors or the publishers under the CC-BY licence.		No permission is required from the authors or the publishers under the CC-BY licence.

			[[Category:Neural Crest]]

Z8600021 at 11:17, 3 March 2015

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	==Overview of Melanocyte Development==		==Overview of Melanocyte Development==

	(A) In mammals, melanoblasts are specified from neural crest cells (NCCs) via a SOX10-positive melanoblast/glial bipotent progenitor. SOX10 expression remains switched on in both of these lineages. Melanoblasts subsequently are specified and acquire MITF, DCT and KIT expression. After colonising the developing embryonic hair follicles, some melanoblasts differentiate into melanocytes and produce the pigment (melanin) that colours the first hair cycle. A subset of melanoblasts dedifferentiate (losing MITF and KIT expression but not DCT) to form melanocyte stem cells in the hair follicle bulge that replenish the differentiated melanocytes via a rapidly proliferating transit-amplifying cell in the subsequent hair cycles. The image on the far right is of a transgenic mouse embryo expressing lacZ under control of the melanoblast promoter Dct. X-Gal staining reveals blue-stained melanoblasts, in particular those migrating from the cervical neural crest and in the head. Also stained are the telencephalon, the dorsal root ganglia (DRG) and the retinal pigmented epithelium of the eye. (B) In zebrafish, there are distinct embryonic and adult pigmentation patterns, as illustrated in the images on the far right. The melanoblasts that form both these patterns originate from a SOX10-positive neural crest-derived progenitor. The embryonic pattern is formed by melanocytes that develop directly from this progenitor via an MITF+ melanoblast. The melanoblasts that form the adult pattern are derived from a melanocyte stem cell population that resides at the dorsal route ganglia (DRG) and is specified by an ERB- and KIT-dependent pathway in the embryo.		'''A''' In mammals, melanoblasts are specified from neural crest cells (NCCs) via a SOX10-positive melanoblast/glial bipotent progenitor. SOX10 expression remains switched on in both of these lineages. Melanoblasts subsequently are specified and acquire MITF, DCT and KIT expression. After colonising the developing embryonic hair follicles, some melanoblasts differentiate into melanocytes and produce the pigment (melanin) that colours the first hair cycle. A subset of melanoblasts dedifferentiate (losing MITF and KIT expression but not DCT) to form melanocyte stem cells in the hair follicle bulge that replenish the differentiated melanocytes via a rapidly proliferating transit-amplifying cell in the subsequent hair cycles. The image on the far right is of a transgenic mouse embryo expressing lacZ under control of the melanoblast promoter Dct. X-Gal staining reveals blue-stained melanoblasts, in particular those migrating from the cervical neural crest and in the head. Also stained are the telencephalon, the dorsal root ganglia (DRG) and the retinal pigmented epithelium of the eye.

			'''B''' In zebrafish, there are distinct embryonic and adult pigmentation patterns, as illustrated in the images on the far right. The melanoblasts that form both these patterns originate from a SOX10-positive neural crest-derived progenitor. The embryonic pattern is formed by melanocytes that develop directly from this progenitor via an MITF+ melanoblast. The melanoblasts that form the adult pattern are derived from a melanocyte stem cell population that resides at the dorsal route ganglia (DRG) and is specified by an ERB- and KIT-dependent pathway in the embryo.


			:'''Links:''' [[Neural Crest - Melanocyte Development\|Melanocyte Development]]

	===Reference===		===Reference===

	<pubmed>25670789</pubmed>		<pubmed>25670789</pubmed>\| [http://dev.biologists.org/content/142/4/620.full?sid=9c0c0b67-790f-42a6-8551-73876896a0d6 Development]

	====Copyright====		====Copyright====

Z8600021: ==Overview of Melanocyte Development== (A) In mammals, melanoblasts are specified from neural crest cells (NCCs) via a SOX10-positive melanoblast/glial bipotent progenitor. SOX10 expression remains switched on in both of these lineages. Melanoblasts s...

2015-03-03T11:15:58Z

New page

==Overview of Melanocyte Development==

(A) In mammals, melanoblasts are specified from neural crest cells (NCCs) via a SOX10-positive melanoblast/glial bipotent progenitor. SOX10 expression remains switched on in both of these lineages. Melanoblasts subsequently are specified and acquire MITF, DCT and KIT expression. After colonising the developing embryonic hair follicles, some melanoblasts differentiate into melanocytes and produce the pigment (melanin) that colours the first hair cycle. A subset of melanoblasts dedifferentiate (losing MITF and KIT expression but not DCT) to form melanocyte stem cells in the hair follicle bulge that replenish the differentiated melanocytes via a rapidly proliferating transit-amplifying cell in the subsequent hair cycles. The image on the far right is of a transgenic mouse embryo expressing lacZ under control of the melanoblast promoter Dct. X-Gal staining reveals blue-stained melanoblasts, in particular those migrating from the cervical neural crest and in the head. Also stained are the telencephalon, the dorsal root ganglia (DRG) and the retinal pigmented epithelium of the eye. (B) In zebrafish, there are distinct embryonic and adult pigmentation patterns, as illustrated in the images on the far right. The melanoblasts that form both these patterns originate from a SOX10-positive neural crest-derived progenitor. The embryonic pattern is formed by melanocytes that develop directly from this progenitor via an MITF+ melanoblast. The melanoblasts that form the adult pattern are derived from a melanocyte stem cell population that resides at the dorsal route ganglia (DRG) and is specified by an ERB- and KIT-dependent pathway in the embryo.

===Reference===

<pubmed>25670789</pubmed>

====Copyright====

Articles published under The Company of Biologists’ Open Access model will be made freely available online via The Company’s website immediately following publication, deposited in PMC for immediate release and can be distributed under the terms of the Creative Commons Attribution (CC-BY) Licence (the terms of which are set out at http://creativecommons.org/licenses/by/3.0/legalcode). Authors retain ownership of the copyright for their article, but undertake to allow anyone to download, reuse, reprint, modify, distribute, and/or copy articles, including for commercial purposes, provided that:

(1) the original authorship is properly and fully attributed and the journal is attributed as the original place of publication with correct citation details given;

(2) if an original work is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this is clearly indicated.

No permission is required from the authors or the publishers under the CC-BY licence.