Literature DB >> 12705872

Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris.

Ana Kljuic1, Hisham Bazzi, John P Sundberg, Amalia Martinez-Mir, Ryan O'Shaughnessy, My G Mahoney, Moise Levy, Xavier Montagutelli, Wasim Ahmad, Vincent M Aita, Derek Gordon, Jouni Uitto, David Whiting, Jurg Ott, Stuart Fischer, T Conrad Gilliam, Colin A B Jahoda, Rebecca J Morris, Andrei A Panteleyev, Vu Thuong Nguyen, Angela M Christiano.   

Abstract

Cell adhesion and communication are interdependent aspects of cell behavior that are critical for morphogenesis and tissue architecture. In the skin, epidermal adhesion is mediated in part by specialized cell-cell junctions known as desmosomes, which are characterized by the presence of desmosomal cadherins, known as desmogleins and desmocollins. We identified a cadherin family member, desmoglein 4, which is expressed in the suprabasal epidermis and hair follicle. The essential role of desmoglein 4 in skin was established by identifying mutations in families with inherited hypotrichosis, as well as in the lanceolate hair mouse. We also show that DSG4 is an autoantigen in pemphigus vulgaris. Characterization of the phenotype of naturally occurring mutant mice revealed disruption of desmosomal adhesion and perturbations in keratinocyte behavior. We provide evidence that desmoglein 4 is a key mediator of keratinocyte cell adhesion in the hair follicle, where it coordinates the transition from proliferation to differentiation.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12705872     DOI: 10.1016/s0092-8674(03)00273-3

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  92 in total

1.  Conditional targeting of E-cadherin in skin: insights into hyperproliferative and degenerative responses.

Authors:  Christopher L Tinkle; Terry Lechler; H Amalia Pasolli; Elaine Fuchs
Journal:  Proc Natl Acad Sci U S A       Date:  2004-01-02       Impact factor: 11.205

2.  A recurrent intragenic deletion mutation in DSG4 gene in three Pakistani families with autosomal recessive hypotrichosis.

Authors:  Muhammad Arshad Rafiq; Muhammad Ansar; Saqib Mahmood; Sayedul Haque; Muhammad Faiyaz-ul-Haque; Suzanne M Leal; Wasim Ahmad
Journal:  J Invest Dermatol       Date:  2004-07       Impact factor: 8.551

Review 3.  New approaches to the representation and analysis of phenotype knowledge in human diseases and their animal models.

Authors:  Paul N Schofield; John P Sundberg; Robert Hoehndorf; Georgios V Gkoutos
Journal:  Brief Funct Genomics       Date:  2011-09       Impact factor: 4.241

4.  The nude mutant gene Foxn1 is a HOXC13 regulatory target during hair follicle and nail differentiation.

Authors:  Christopher S Potter; Nathanael D Pruett; Michael J Kern; Mary Ann Baybo; Alan R Godwin; Kathleen A Potter; Ron L Peterson; John P Sundberg; Alexander Awgulewitsch
Journal:  J Invest Dermatol       Date:  2010-12-30       Impact factor: 8.551

5.  Primary follicular dystrophy with scarring dermatitis in C57BL/6 mouse substrains resembles central centrifugal cicatricial alopecia in humans.

Authors:  J P Sundberg; D Taylor; G Lorch; J Miller; K A Silva; B A Sundberg; D Roopenian; L Sperling; D Ong; L E King; H Everts
Journal:  Vet Pathol       Date:  2010-09-22       Impact factor: 2.221

Review 6.  Non-infectious environmental antigens as a trigger for the initiation of an autoimmune skin disease.

Authors:  Ye Qian; Donna A Culton; Joseph S Jeong; Nicole Trupiano; Jesus G Valenzuela; Luis A Diaz
Journal:  Autoimmun Rev       Date:  2016-07-08       Impact factor: 9.754

Review 7.  Pemphigus: a Comprehensive Review on Pathogenesis, Clinical Presentation and Novel Therapeutic Approaches.

Authors:  Robert Pollmann; Thomas Schmidt; Rüdiger Eming; Michael Hertl
Journal:  Clin Rev Allergy Immunol       Date:  2018-02       Impact factor: 8.667

8.  Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families.

Authors:  Naveed Wasif; Syed Kamran ul-Hassan Naqvi; Sulman Basit; Nadir Ali; Muhammad Ansar; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-12-28       Impact factor: 4.132

9.  Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23–22.3.

Authors:  Gul Naz; Ghazanfar Ali; Syed Kamran-ul-Hassan Naqvi; Zahid Azeem; Wasim Ahmad
Journal:  Hum Genet       Date:  2010-04       Impact factor: 4.132

10.  Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.

Authors:  Sandra M Pasternack; Melanie Refke; Elham Paknia; Hans Christian Hennies; Thomas Franz; Niklas Schäfer; Alan Fryer; Maurice van Steensel; Elizabeth Sweeney; Miquel Just; Clemens Grimm; Roland Kruse; Carlos Ferrándiz; Markus M Nöthen; Utz Fischer; Regina C Betz
Journal:  Am J Hum Genet       Date:  2012-12-13       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.