Large-Scale Electron Microscopy Maps of Patient Skin and Mucosa Provide Insight into Pathogenesis of Blistering Diseases

被引:64
作者
Sokol, Ena [1 ,2 ]
Kramer, Duco [2 ]
Diercks, Gilles F. H. [2 ]
Kuipers, Jeroen [1 ]
Jonkman, Marcel F. [2 ]
Pas, Hendri H. [2 ]
Giepmans, Ben N. G. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Cell Biol, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Dermatol, Ctr Blistering Dis, Groningen, Netherlands
关键词
PEMPHIGUS-VULGARIS; BULLOUS IMPETIGO; DESMOGLEIN; ACANTHOLYSIS; ULTRASTRUCTURE; KERATINOCYTES; FOLIACEUS; BINDING; CELLS; IGG;
D O I
10.1038/jid.2015.109
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Large-scale electron microscopy ("nanotomy") allows straight forward ultrastructural examination of tissue, cells, organelles, and macromolecules in a single data set. Such data set equals thousands of conventional electron microscopy images and is freely accessible (www.nanotomy.org). The software allows zooming in and out of the image from total overview to nanometer scale resolution in a 'Google Earth' approach. We studied the life-threatening human autoimmune blistering disease pemphigus, using nanotomy. The pathomechanism of cell-cell separation (acantholysis) that underlies the blistering is poorly understood. Ultrastructural examination of pemphigus tissue revealed previously unreported findings: (i) the presence of double-membrane structures between cells in all pemphigus types; (ii) the absence of desmosomes around spontaneous blisters in pemphigus foliaceus (PF); (iii) lower level blistering in PF when force induced; and (iv) intercellular widening at non-acantholytic cell layers. Thus, nanotomy delivers open-source electron microscopic maps of patient tissue, which can be analyzed for additional anomalies from any computer by experts from different fields.
引用
收藏
页码:1763 / 1770
页数:8
相关论文
共 26 条
[1]   Staphylococcal scalded skin syndrome: loss of desmoglein 1 in patient skin [J].
Aalfs, A. Susanne ;
Oktarina, D. A. Mira ;
Diercks, Gilles F. H. ;
Jonkman, Marcel F. ;
Pas, Hendri H. .
EUROPEAN JOURNAL OF DERMATOLOGY, 2010, 20 (04) :451-456
[2]   AUTOANTIBODIES AGAINST THE AMINO-TERMINAL CADHERIN-LIKE BINDING DOMAIN OF PEMPHIGUS-VULGARIS ANTIGEN ARE PATHOGENIC [J].
AMAGAI, M ;
KARPATI, S ;
PRUSSICK, R ;
KLAUSKOVTUN, V ;
STANLEY, JR .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (03) :919-926
[3]   Desmoglein as a Target in Skin Disease and Beyond [J].
Amagai, Masayuki ;
Stanley, John R. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2012, 132 (03) :776-784
[4]   Binding of pemphigus vulgaris IgG to antigens in desmosome core domains excludes immune complexes rather than directly splitting desmosomes [J].
Aoyama, Y. ;
Nagai, M. ;
Kitajima, Y. .
BRITISH JOURNAL OF DERMATOLOGY, 2010, 162 (05) :1049-1055
[5]   Disadhesion of epidermal keratinocytes: A histologic clue to palmoplantar keratodermas caused by DSG1 mutations [J].
Bergman, Reuven ;
Hershkovitz, Dov ;
Fuchs, Dana ;
Indelman, Margarita ;
Gadot, Yael ;
Sprecher, Eli .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2010, 62 (01) :107-113
[6]   A novel explanation for acantholysis in pemphigus vulgaris: The basal cell shrinkage hypothesis [J].
Bystryn, JC ;
Grando, SA .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2006, 54 (03) :513-516
[7]   The Desmosome [J].
Delva, Emmanuella ;
Tucker, Dana K. ;
Kowalczyk, Andrew P. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2009, 1 (02) :a002543
[8]   CONTINUAL ASSEMBLY OF HALF-DESMOSOMAL STRUCTURES IN THE ABSENCE OF CELL CONTACTS AND THEIR FRUSTRATED ENDOCYTOSIS - A COORDINATED SISYPHUS CYCLE [J].
DEMLEHNER, MP ;
SCHAFER, S ;
GRUND, C ;
FRANKE, WW .
JOURNAL OF CELL BIOLOGY, 1995, 131 (03) :745-760
[9]   The ultrastructure of acantholysis in pemphigus vulgaris [J].
Diercks, G. F. H. ;
Pas, H. H. ;
Jonkman, M. F. .
BRITISH JOURNAL OF DERMATOLOGY, 2009, 160 (02) :460-461
[10]   Desmosome structure, composition and function [J].
Garrod, David ;
Chidgey, Martyn .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2008, 1778 (03) :572-587