Literature DB >> 9088920

Basement membranes and pulmonary development.

P L Sannes1, J Wang.   

Abstract

Basement membranes (BM) are specialized extracellular matrices (ECM) which serve as complex interfaces between epithelia, peripheral nerves, or muscle cells and their surrounding tissue microenvironments. Their composition is known to include type IV collagen, laminin, entactin, heparan sulfate proteoglycan (HSPG, perlecan), and chondroitin sulfate proteoglycan (CSPG). By immunohistochemistry, collagen IV, laminin, and entactin are detectable from day 14 of gestation on, and become progressively more prominent with time. Perleaan has not been examined in prentatal lungs, but is widely distributed and abundant in all lung MBs from birth throughout development. CSPG has a somewhat discontinuous and lightly reactive appearance in alveolar BMs at birth but the staining becomes continuous and darker in the adult. This contrasts with glycosaminoglycan, chondroitin sulfate, which is prominently expressed in prenatal and early postnatal stages, but progressively diminishes with advancing development. As an interface between cell populations and surrounding ECMs, BMs act as a physical barrier to some cells and molecules, while serving as attachment points and binding sites for others. Basic fibroblast growth factor is an example of the latter, because it localizes with all BM components by immunostaining throughout development and reflects the multifactorial array of potential effectors in the complex processes of proliferation and differentiation.

Entities:  

Mesh:

Year:  1997        PMID: 9088920     DOI: 10.3109/01902149709074023

Source DB:  PubMed          Journal:  Exp Lung Res        ISSN: 0190-2148            Impact factor:   2.459


  7 in total

1.  Identification of glycosaminoglycans in human airway secretions.

Authors:  Maria E Monzon; Susana M Casalino-Matsuda; Rosanna M Forteza
Journal:  Am J Respir Cell Mol Biol       Date:  2005-09-29       Impact factor: 6.914

Review 2.  Basement membranes in the cornea and other organs that commonly develop fibrosis.

Authors:  Paramananda Saikia; Carla S Medeiros; Shanmugapriya Thangavadivel; Steven E Wilson
Journal:  Cell Tissue Res       Date:  2018-10-03       Impact factor: 5.249

3.  Up-regulation of heparan sulfate 6-O-sulfation in idiopathic pulmonary fibrosis.

Authors:  Jingning Lu; Linda Auduong; Eric S White; Xinping Yue
Journal:  Am J Respir Cell Mol Biol       Date:  2014-01       Impact factor: 6.914

4.  The involvement of the laminin-integrin α7β1 signaling pathway in mechanical ventilation-induced pulmonary fibrosis.

Authors:  Han-Di Liao; Yong Mao; You-Guo Ying
Journal:  J Thorac Dis       Date:  2017-10       Impact factor: 2.895

Review 5.  Implications for Extracellular Matrix Interactions With Human Lung Basal Stem Cells in Lung Development, Disease, and Airway Modeling.

Authors:  Shana M Busch; Zareeb Lorenzana; Amy L Ryan
Journal:  Front Pharmacol       Date:  2021-05-12       Impact factor: 5.810

6.  Laminin-332 alters connexin profile, dye coupling and intercellular Ca2+ waves in ciliated tracheal epithelial cells.

Authors:  Brant E Isakson; Colin E Olsen; Scott Boitano
Journal:  Respir Res       Date:  2006-08-02

Review 7.  A pathologic two-way street: how innate immunity impacts lung fibrosis and fibrosis impacts lung immunity.

Authors:  Helen I Warheit-Niemi; Elissa M Hult; Bethany B Moore
Journal:  Clin Transl Immunology       Date:  2019-06-26
  7 in total

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