Tissue distribution of perlecan domains III and V during embryonic and fetal human development

被引:0
作者
Roediger, Matthias [1 ]
Kruegel, Jenny [1 ]
Miosge, Nicolai [1 ]
Gersdorff, Nikolaus [1 ]
机构
[1] Univ Gottingen, Tissue Regenerat Work Grp, Dept Prosthodont, D-37075 Gottingen, Germany
关键词
Perlecan; Basement membrane; Human embryogenesis; Immunohistochemistry; HEPARAN-SULFATE PROTEOGLYCAN; SCHWARTZ-JAMPEL-SYNDROME; BASEMENT-MEMBRANES; CELL-ADHESION; EXPRESSION; LAMININ; BINDS; FIBULIN-2; NIDOGEN; LOCALIZATION;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A major component of basement membranes (BMs) is perlecan, a five-domain heparan sulphate proteoglycan. During murine embryogenesis, nearly all BMs of mesenchymal origin express perlecan, and it is believed to participate in the supramolecular assembly of BMs. However, the distribution of perlecan in human embryonic and fetal tissues is widely unknown, except for cartilage anlagen of developing extremities and the fetal spine. Clinical syndromes, caused by perlecan-associated mutations or gene-defects, suggest its multifunctional involvement during human development. Here we reveal the immunohistochemistry of perlecan domains III and V during human development from gestational weeks (gw) 6 to 12 in basement membrane zones (BMZs) of the developing brain, nervous system, blood vessels, skin, lung, heart, kidney, liver, intestine and skeletal system. Interestingly, a difference in the distribution of the two perlecan domains was found in the endoneurium of ganglia. Domain III is strongly present from gw 6 onwards, while domain V shows attenuated expression at this stage and has been detected abundantly only from gw 8 onwards, possibly indicating vascularization of the endoneurium during this early stage. We found perlecan to be present particularly at those stages of human development where epithelial-mesenchymal interactions occur.
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页码:859 / 868
页数:10
相关论文
共 53 条
[11]   Perlecan maintains the integrity of cartilage and some basement membranes [J].
Costell, M ;
Gustafsson, E ;
Aszódi, A ;
Mörgelin, M ;
Bloch, W ;
Hunziker, E ;
Addicks, K ;
Timpl, R ;
Fässler, R .
JOURNAL OF CELL BIOLOGY, 1999, 147 (05) :1109-1122
[12]   ANTIBODY MAPPING AND TISSUE LOCALIZATION OF GLOBULAR AND CYSTEINE-RICH REGIONS OF PERLECAN DOMAIN-III [J].
COUCHMAN, JR ;
LJUBIMOV, AV ;
STHANAM, M ;
HORCHAR, T ;
HASSELL, JR .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1995, 43 (09) :955-963
[13]   Expression of the heparan sulfate proteoglycan, perlecan, during mouse embryogenesis and perlecan chondrogenic activity in vitro [J].
French, MM ;
Smith, SE ;
Akanbi, K ;
Sanford, T ;
Hecht, J ;
Farach-Carson, MC ;
Carson, DD .
JOURNAL OF CELL BIOLOGY, 1999, 145 (05) :1103-1115
[14]   Structural basis of glycosaminoglycan modification and of heterotypic interactions of perlecan domain V [J].
Friedrich, MVK ;
Göhring, W ;
Mörgelin, M ;
Brancaccio, A ;
David, G ;
Timpl, R .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 294 (01) :259-270
[15]   Laminin γ3 chain binds to nidogen and is located in murine basement membranes [J].
Gersdorff, N ;
Kohfeldt, E ;
Sasaki, T ;
Timpl, R ;
Miosge, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (23) :22146-22153
[16]   Perlecan controls neurogenesis in the developing telencephalon [J].
Giros, Amparo ;
Morante, Javier ;
Gil-Sanz, Cristina ;
Fairen, Alfonso ;
Costell, Mercedes .
BMC DEVELOPMENTAL BIOLOGY, 2007, 7
[17]   BMP-1/tolloid-like metalloproteases process endorepellin, the angiostatic C-terminal fragment of perlecan [J].
Gonzalez, EM ;
Reed, CC ;
Bix, G ;
Fu, J ;
Zhang, Y ;
Gopalakrishnan, B ;
Greenspan, DS ;
Iozzo, RV .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (08) :7080-7087
[18]   INDUCTIVE TISSUE INTERACTION IN DEVELOPMENT [J].
GROBSTEIN, C .
ADVANCES IN CANCER RESEARCH, 1956, 4 :187-236
[19]  
Handler M, 1997, DEV DYNAM, V210, P130, DOI 10.1002/(SICI)1097-0177(199710)210:2<130::AID-AJA6>3.0.CO
[20]  
2-H