Literature DB >> 9226037

Changing patterns of cell adhesion molecules during mouse pelage hair follicle development. 2. Follicle morphogenesis in the hair mutants, Tabby and downy.

U Vielkind1, M H Hardy.   

Abstract

Wild-type mice have three main types of hair in their pelage: tylotrichs, awls and zigzags. Tabby mice have a yellowish coat consisting of awls only, whereas downy mice have a sparse grayish coat consisting of unusually fine hairs. The spatial and temporal distribution of cell adhesion molecules (CAMs) during hair follicle morphogenesis was investigated in the mutants and compared with that in nonmutant mice. In Tabby embryos, awl follicles developed normally and showed normal immunostaining patterns for E-cadherin, P-cadherin and N-CAM. Prior to follicle initiation, however, some deviations from normal skin morphology and staining patterns indicated a delay in the development of the basal epidermal layer. On the other hand, the stratum corneum was formed prematurely. Therefore, the lack of tylotrich and zigzag follicles in Tabby mice might be explained by a general defect in epidermal development rather than by abnormal CAM expression. In downy embryos, tylotrich and awl follicles were initiated within the normal time periods, but elongation and differentiation of most follicles were abnormal. At birth, most follicles were small and/or severely deformed but showed normal CAM expression patterns. Extreme distortion and disorientation of follicles seemed to be associated with disintegration of the dermal papilla and abnormal mesenchymal cell condensations between the follicles. This suggests that abnormal hair development in downy mice might result from a defect in dermal rather than epidermal components of the skin.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9226037     DOI: 10.1159/000147880

Source DB:  PubMed          Journal:  Acta Anat (Basel)        ISSN: 0001-5180


  14 in total

Review 1.  EDA signaling and skin appendage development.

Authors:  Chang-Yi Cui; David Schlessinger
Journal:  Cell Cycle       Date:  2006-09-14       Impact factor: 4.534

Review 2.  Touch sense: functional organization and molecular determinants of mechanosensitive receptors.

Authors:  Yann Roudaut; Aurélie Lonigro; Bertrand Coste; Jizhe Hao; Patrick Delmas; Marcel Crest
Journal:  Channels (Austin)       Date:  2012 Jul-Aug       Impact factor: 2.581

Review 3.  Developing a sense of touch.

Authors:  Blair A Jenkins; Ellen A Lumpkin
Journal:  Development       Date:  2017-11-15       Impact factor: 6.868

4.  X-linked anhidrotic ectodermal dysplasia disruption yields a mouse model for ocular surface disease and resultant blindness.

Authors:  Chang-Yi Cui; Janine A Smith; David Schlessinger; Chi-Chao Chan
Journal:  Am J Pathol       Date:  2005-07       Impact factor: 4.307

5.  Bone morphogenetic protein signaling regulates postnatal hair follicle differentiation and cycling.

Authors:  Udayan Guha; Lars Mecklenburg; Pamela Cowin; Lixin Kan; W Michael O'Guin; Dolores D'Vizio; Richard G Pestell; Ralf Paus; John A Kessler
Journal:  Am J Pathol       Date:  2004-09       Impact factor: 4.307

6.  Dkk4 and Eda regulate distinctive developmental mechanisms for subtypes of mouse hair.

Authors:  Chang-Yi Cui; Makoto Kunisada; Yulan Piao; Victoria Childress; Minoru S H Ko; David Schlessinger
Journal:  PLoS One       Date:  2010-04-01       Impact factor: 3.240

7.  Analysis of the temporal requirement for eda in hair and sweat gland development.

Authors:  Chang-Yi Cui; Makoto Kunisada; Diana Esibizione; Eric G Douglass; David Schlessinger
Journal:  J Invest Dermatol       Date:  2008-10-16       Impact factor: 8.551

8.  TRAF6-deficient mice display hypohidrotic ectodermal dysplasia.

Authors:  Asuka Naito; Hisahiro Yoshida; Eri Nishioka; Mizuho Satoh; Sakura Azuma; Tadashi Yamamoto; Shin-ichi Nishikawa; Jun-ichiro Inoue
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

9.  Morpho-regulation of ectodermal organs: integument pathology and phenotypic variations in K14-Noggin engineered mice through modulation of bone morphogenic protein pathway.

Authors:  Maksim Plikus; Wen Pin Wang; Jian Liu; Xia Wang; Ting-Xin Jiang; Cheng-Ming Chuong
Journal:  Am J Pathol       Date:  2004-03       Impact factor: 4.307

10.  A spontaneous Fatp4/Scl27a4 splice site mutation in a new murine model for congenital ichthyosis.

Authors:  Jianning Tao; Maranke I Koster; Wilbur Harrison; Jennifer L Moran; David R Beier; Dennis R Roop; Paul A Overbeek
Journal:  PLoS One       Date:  2012-11-30       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.