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Colour dilution alopecia in seven Dachshunds. A clinical study and the hereditary, microscopical and ultrastructural aspect of the disease.七只腊肠犬的毛色稀释性脱毛症。一项关于该疾病的临床研究以及遗传、显微镜和超微结构方面的研究
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Colour Dilution Alopecia (CDA) in Ten yorkshire Terriers.十只约克夏梗犬的毛色稀释性脱毛症
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Polymorphisms within the canine MLPH gene are associated with dilute coat color in dogs.犬类MLPH基因内的多态性与犬的稀释毛色有关。
BMC Genet. 2005 Jun 16;6:34. doi: 10.1186/1471-2156-6-34.
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Genetics of pigmentary disorders.色素沉着紊乱的遗传学
Am J Med Genet C Semin Med Genet. 2004 Nov 15;131C(1):75-81. doi: 10.1002/ajmg.c.30036.
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Rab GTPases and myosin motors in organelle motility.细胞器运动中的Rab GTP酶和肌球蛋白马达
Traffic. 2004 Jun;5(6):393-9. doi: 10.1111/j.1398-9219.2004.00190.x.
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Melanosome transfer to and translocation in the keratinocyte.黑素小体向角质形成细胞的转移及在其中的转运。
Exp Dermatol. 2003;12 Suppl 2:5-12. doi: 10.1034/j.1600-0625.12.s2.1.x.
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Organelle transport: a park-and-ride system for melanosomes.
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8
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).局限于色素减退的格里塞利综合征由黑色素亲和蛋白缺陷(GS3型)或MYO5A基因F外显子缺失(GS1型)引起。
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9
CIOMS International Guiding Principles for Biomedical Research Involving Animals.《国际医学科学组织理事会关于涉及动物的生物医学研究的国际指导原则》
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10
Mutations in Mlph, encoding a member of the Rab effector family, cause the melanosome transport defects observed in leaden mice.编码Rab效应蛋白家族成员的Mlph发生突变,会导致在铅灰小鼠中观察到的黑素小体运输缺陷。
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大型明斯特兰犬的黑色毛囊发育不良:临床、组织学和超微结构特征

Black hair follicular dysplasia in Large Münsterländer dogs: clinical, histological and ultrastructural features.

作者信息

von Bomhard Wolf, Mauldin Elizabeth A, Schmutz Sheila M, Leeb Tosso, Casal Margret L

机构信息

Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, 19104, USA.

出版信息

Vet Dermatol. 2006 Jun;17(3):182-8. doi: 10.1111/j.1365-3164.2006.00517.x.

DOI:10.1111/j.1365-3164.2006.00517.x
PMID:16674733
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3330242/
Abstract

Four Large Münsterländer cross-bred dogs affected with black hair follicular dysplasia (BHFD) and one unaffected control littermate were observed, and skin was sampled weekly over the first 19 weeks of life. Affected dogs were born with silvery grey hair, a consequence of melanin clumping in the hair shafts. Hair bulb melanocytes were densely pigmented, and contained abundant stage IV melanosomes but adjacent matrix keratinocytes lacked melanosomes. Melanin clumping was not prominent in epidermal melanocytes in the haired skin but occurred in the foot pads. Follicular changes progressed from bulbar clumping, clumping in the isthmus/infundibulum and finally to dysplastic hair shafts. Alopecia developed progressively in pigmented areas. Silver-grey hair, melanin clumping, accumulation of stage IV melanosomes within melanocytes and insufficient melanin transfer to adjacent keratinocytes are also classic features of human Griscelli syndrome. The underlying cause in Griscelli syndrome is a defect of melanocytic intracellular transport proteins leading to inadequate and disorganized melanosome transfer to keratinocytes with resultant melanin clumping. In view of the correlation in the phenotype, histology and ultrastructure between both disorders, a defect in intracellular melanosome transport is postulated as the pathogenic mechanism in BHFD.

摘要

观察了4只患有黑色毛囊发育不良(BHFD)的大型明斯特兰德杂交犬和1只未受影响的同窝对照犬,并在其出生后的前19周每周采集皮肤样本。患病犬出生时毛发为银灰色,这是毛干中黑色素聚集的结果。毛球黑素细胞色素沉着浓密,含有丰富的IV期黑素小体,但相邻的基质角质形成细胞缺乏黑素小体。在有毛皮肤的表皮黑素细胞中,黑色素聚集不明显,但在脚垫中出现。毛囊变化从球部聚集、峡部/漏斗部聚集,最终发展为发育异常的毛干。色素沉着区域逐渐出现脱发。银灰色毛发、黑色素聚集、黑素细胞内IV期黑素小体的积累以及黑色素向相邻角质形成细胞的转移不足也是人类格里塞利综合征的典型特征。格里塞利综合征的根本原因是黑素细胞内转运蛋白缺陷,导致黑素小体向角质形成细胞的转运不足且紊乱,从而导致黑色素聚集。鉴于两种疾病在表型、组织学和超微结构上的相关性,推测细胞内黑素小体转运缺陷是BHFD的致病机制。