Literature DB >> 11356147

Glycosaminoglycans in the study of mammalian organ development.

J A Davies1, C E Fisher, M W Barnett.   

Abstract

Glycosaminoglycans (GAGs) are linear polymers of amino sugar uronic acid disaccharides, and are generally attached to protein cores to form proteoglycans. GAGs interact with a large number of proteins and can participate in matrix organization, cell adhesion, differentiation, growth and apoptosis. Proteoglycans are expressed in tightly regulated spatio-temporal patterns during organ development, and changes in expression frequently correlate with developmental events. Here we review the evidence that GAGs play important roles in the development of mouse kidneys, which are organs that will undergo organotypic development in simple culture conditions and that are therefore highly accessible to experimentation. Depleting kidneys of GAGs, either biochemically or genetically, blocks the development of the urinary collecting-duct system, probably because critical signalling molecules require GAGs to form stable associations with their receptors. The insensitivity of GAG-deprived organ rudiments to physiological concentrations of growth factors can be used to screen candidate signalling molecules for morphoregulatory activity; candidate growth factors are applied at supraphysiological levels to GAG-deprived kidneys and assessed for their ability to rescue normal development. This approach has assisted the identification of four collecting-duct morphogens: hepatocyte growth factor, glial cell line-derived neurotrophic factor, nerturin and persephin.

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Year:  2001        PMID: 11356147     DOI: 10.1042/0300-5127:0290166

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  4 in total

1.  Structural remodeling of proteoglycans upon retinoic acid-induced differentiation of NCCIT cells.

Authors:  Leyla Gasimli; Hope E Stansfield; Alison V Nairn; Haiying Liu; Janet L Paluh; Bo Yang; Jonathan S Dordick; Kelley W Moremen; Robert J Linhardt
Journal:  Glycoconj J       Date:  2012-10-02       Impact factor: 2.916

2.  Cell surface glycoconjugate abnormalities and corneal epithelial wound healing in the pax6+/- mouse model of aniridia-related keratopathy.

Authors:  Romana Kucerova; Jingxing Ou; Diane Lawson; Lucy J Leiper; J Martin Collinson
Journal:  Invest Ophthalmol Vis Sci       Date:  2006-12       Impact factor: 4.799

3.  Effects of modifiers of glycosaminoglycan biosynthesis on outflow facility in perfusion culture.

Authors:  Kate E Keller; John M Bradley; Mary J Kelley; Ted S Acott
Journal:  Invest Ophthalmol Vis Sci       Date:  2008-06       Impact factor: 4.799

4.  Low molecular weight heparin may benefit nephrotic remission in steroid‑sensitive nephrotic syndrome via inhibiting elastase.

Authors:  Songhui Zhai; Lijuan Hu; Lin Zhong; Yuhong Tao; Zheng Wang
Journal:  Mol Med Rep       Date:  2017-10-03       Impact factor: 2.952

  4 in total

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