Literature DB >> 2712351

Ultrastructure of a model basement membrane lacking type IV collagen.

P R Brauer1, J M Keller.   

Abstract

Basement membranes (BMs) are specialized extracellular matrices which have important roles in cell attachment, migration, growth, and differentiation. The major components of these matrices include type IV collagen, laminin, entactin, and heparan sulfate proteoglycan. The framework or scaffold of BMs has been proposed to be type IV collagen (Yurchenco et al., 1986, J. Histochem. Cytochem., 34:93-102). However, a murine teratocarcinoma cell-line, M1536-B3, has been described which produces an extracellular matrix (ECM) composed of some of the known components of BM, e.g., laminin, entactin, and sulfated proteoglycan, but lacking type IV collagen (Chung et al., 1979, Cell, 16:277-287). With the use of morphological techniques, we have found that the ECM assembled by these cells is composed of multiple layers of electron-dense cords arranged in an interweaving meshwork with short 2-4 nm-diameter cylindrical rods embedded throughout. This organization closely resembles that reported for naturally occurring BMs, e.g., Reichert's membrane (Inoué et al., 1983, J. Cell Biol., 97: 1524-1537). The previous identification of known in vivo BM components in M1536-B3 ECM and the correspondence in morphological appearance of M1536-B3 ECM with that present in naturally occurring BMs suggests that a BM-type of ECM can be assembled without a type IV collagen framework, thus indicating that other components of BMs have a critical role in BM organization and assembly.

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Year:  1989        PMID: 2712351     DOI: 10.1002/ar.1092230405

Source DB:  PubMed          Journal:  Anat Rec        ISSN: 0003-276X


  8 in total

1.  Extracellular matrix in the rat spiral limbus.

Authors:  K Ishii; C Schröter-Kermani; D Xu; H J Merker; V Jahnke
Journal:  Eur Arch Otorhinolaryngol       Date:  1992       Impact factor: 2.503

2.  VP23R of infectious spleen and kidney necrosis virus mediates formation of virus-mock basement membrane to provide attaching sites for lymphatic endothelial cells.

Authors:  Xiaopeng Xu; Shaoping Weng; Ting Lin; Junliang Tang; Lichao Huang; Jing Wang; Xiaoqiang Yu; Ling Lu; Zhijian Huang; Jianguo He
Journal:  J Virol       Date:  2010-09-01       Impact factor: 5.103

3.  Ultrastructural localization of lectin-binding sites in different basement membranes.

Authors:  M Salamat; W Götz; J Werner; R Herken
Journal:  Histochem J       Date:  1993-06

4.  A line of rat ovarian surface epithelium provides a continuous source of complex extracellular matrix.

Authors:  P A Kruk; N Auersperg
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-04       Impact factor: 2.416

5.  Laminin forms an independent network in basement membranes.

Authors:  P D Yurchenco; Y S Cheng; H Colognato
Journal:  J Cell Biol       Date:  1992-06       Impact factor: 10.539

6.  Type IV collagen is detectable in most, but not all, basement membranes of Caenorhabditis elegans and assembles on tissues that do not express it.

Authors:  P L Graham; J J Johnson; S Wang; M H Sibley; M C Gupta; J M Kramer
Journal:  J Cell Biol       Date:  1997-06-02       Impact factor: 10.539

7.  Terminal short arm domains of basement membrane laminin are critical for its self-assembly.

Authors:  J C Schittny; P D Yurchenco
Journal:  J Cell Biol       Date:  1990-03       Impact factor: 10.539

8.  Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation.

Authors:  N Smyth; H S Vatansever; P Murray; M Meyer; C Frie; M Paulsson; D Edgar
Journal:  J Cell Biol       Date:  1999-01-11       Impact factor: 10.539

  8 in total

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