Literature DB >> 2653200

Epidermal growth factor and the kidney.

D A Fisher1, E C Salido, L Barajas.   

Abstract

Current information indicates that the mammalian kidney is a significant site of EGF synthesis, second only to the salivary gland in the rodent and probably exceeding most other tissues in the human species. The prepro EGF mRNA is localized to the cells of the TALH and the DCT. The EGF mRNA transcript in kidney is similar to that in salivary gland; the molecular mass of the prepro EGF protein in kidney approximates 130,000 kDa. Several EGF peptides are excreted in urine, including 6000-molecular weight peptides (composed of EGF 1-53, 1-52, 1-51, and 1-50) and a 30,000-molecular weight species with an aminoterminus portion corresponding to amino acids 829-848 of the prepro molecule. It has been suggested that prepro EGF could be a membrane protein since it contains an internal hydrophobic domain (amino acids 1039-1058) adjacent to the EGF sequence (amino acids 976-1029). The 30,000-molecular weight urinary product appears to represent a protein derived from amino acids 829 to approximately 1029 of prepro EGF, adjacent (distal) to the hydrophobic domain. Moreover, immunoelectron microscopy localizes the EGF immunoreactivity to the apical plasma membrane of the TALH and DCT cells. The molecular form of this apically localized, EGF immunoreactivity is not yet clear. Proximal, distal, and TALH cells of the renal tubules and renal medullary interstitial cells appear to have EGF receptors and respond to EGF with increased DNA synthesis and mitogenesis. Also, there is a relatively late increase in prepro EGF mRNA levels in TALH and DCT cells during the process of renal hypertrophy. Limited evidence suggests a role of EGF on tubular function mediated via basal EGF receptors. EGF peptides processed intracellularly or by membrane localized peptidases appear to be continuously excreted and secreted into urine from the apical membrane surface of the TALH and DCT cells. This urinary EGF is constantly bathing urinary tract epithelial surfaces and could play a role in maintaining surface integrity. A similar role for salivary gland EGF in saliva has been proposed for the gastrointestinal tract. It also is possible that prepro EGF is anchored in the apical membrane, where it could function as a receptor, and a role for renal tubular EGF in regulation of membrane transport events has been proposed.

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Year:  1989        PMID: 2653200     DOI: 10.1146/annurev.ph.51.030189.000435

Source DB:  PubMed          Journal:  Annu Rev Physiol        ISSN: 0066-4278            Impact factor:   19.318


  36 in total

Review 1.  Polypeptide growth factors and the kidney: a developmental perspective.

Authors:  E D Avner
Journal:  Pediatr Nephrol       Date:  1990-07       Impact factor: 3.714

2.  "Tissue" transglutaminase is specifically expressed in neonatal rat liver cells undergoing apoptosis upon epidermal growth factor-stimulation.

Authors:  M Piacentini; F Autuori; L Dini; M G Farrace; L Ghibelli; L Piredda; L Fesus
Journal:  Cell Tissue Res       Date:  1991-02       Impact factor: 5.249

Review 3.  Function and regulation of TRPP2 at the plasma membrane.

Authors:  Leonidas Tsiokas
Journal:  Am J Physiol Renal Physiol       Date:  2009-02-25

Review 4.  Renal growth in infancy and childhood--experimental studies of regulatory mechanisms.

Authors:  S H Larsson; A Aperia
Journal:  Pediatr Nephrol       Date:  1991-07       Impact factor: 3.714

5.  Blocking EGFR in the liver improves the tumor-to-liver uptake ratio of radiolabeled EGF.

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Journal:  Tumour Biol       Date:  2010-01-30

6.  Analysis of WT1 gene expression during mouse nephrogenesis in organ culture.

Authors:  H Yeger; D Forget; J Alami; B R Williams
Journal:  In Vitro Cell Dev Biol Anim       Date:  1996-09       Impact factor: 2.416

7.  Localization of epidermal growth factor (EGF) binding sites on antiluminal plasma membrane of rat kidney: autoradiographic study using nonfiltering perfused rat kidney.

Authors:  D C Kim; Y Sugiyama; Y Kanai; N Ohnuma; M Hanano
Journal:  Pharm Res       Date:  1992-01       Impact factor: 4.200

8.  The cytoplasmic domain of proEGF negatively regulates motility and elastinolytic activity in thyroid carcinoma cells.

Authors:  Aleksandra Glogowska; Janette Pyka; Astrid Kehlen; Marek Los; Paul Perumal; Ekkehard Weber; Sheue-yann Cheng; Cuong Hoang-Vu; Thomas Klonisch
Journal:  Neoplasia       Date:  2008-10       Impact factor: 5.715

9.  Expression of epidermal growth factor in the rat kidney. An immunocytochemical and in situ hybridization study.

Authors:  E C Salido; J Lakshmanan; D A Fisher; L J Shapiro; L Barajas
Journal:  Histochemistry       Date:  1991

10.  Apical epidermal growth factor receptor signaling: regulation of stretch-dependent exocytosis in bladder umbrella cells.

Authors:  Elena M Balestreire; Gerard Apodaca
Journal:  Mol Biol Cell       Date:  2007-02-07       Impact factor: 4.138

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