Literature DB >> 34004101

[Cystic fibrosis being a polyendocrine disease (Review)].

N B Chagay1, G Ya Khayt1, T M Vdovina2, A A Shaforost2.   

Abstract

The cystic fibrosis transmembrane regulator (CFTR) gene encodes the synthesis of a protein of the same name, which functions as a direct activator of anionic transport. Chloride is the most abundant anion; as an antagonist of Na+ and K+, it provides electroneutrality of cell membranes at rest; together with cations, it serves as an important osmolyte and forms water flow across cell membranes for transepithelial secretion.Glandular cells in CF trap Cl- and Na+, and the prodused secretion is excessively viscous. Subnormal CFTR activity leads to stagnation of mucociliary clearance, inhibition of intestinal transport.In addition to exocrine disorders, CFTR mutations are associated with a decrease in volume, mass, increased apoptosis of β-cells of the pancreas, a significant suppression of insulin exocytosis in response to stimulation with glucose and glucagon-like peptide-1, hyperglucagonemia against the background of a defect in the suppression of α-cell function by insulin, but a decrease in maximum capacity α-cells.Deficiency and progressive decline in bone mineral density is an expected secondary manifestation of CF due to pancreatic exocrine insufficiency with malabsorption of nutrients and fat-soluble vitamins. However, in patients with the F508del mutation, a significant decrease in the synthesis of OPG, COX-2, PGE2 in the osteoblastic formation, and an increase in the activity of the antianabolic NF-kB were found. We are talking about a defect in the canonical signaling pathway (Wnt/β-catenin), which regulates the expression of genes-activators of osteoblastogenesis, dissociation of the stages of physiological bone remodeling.In addition to congenital bilateral or unilateral aplasia of the vas deferens, an increase in the frequency of CFTR mutations is also found in non-obstructive azoospermia, oligo-, astheno- and teratospermia. CFTR is involved in the entry of HCO3- into Sertoli cells to trigger cAMP-dependent transcription and its defects lead to suppression of FSH-dependent gene expression of spermatogenesis, loss of sequence in the Wnt cascade, destruction of the PGE2-dependent transepithelial interaction and, as a consequence, the blood-testicular barrier.CF is characterized, along with classical signs, by endocrine dysfunction of the pancreas, osteoporosis with suppression of osteoblastogenesis, and a defect in spermatogenesis.

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Year:  2021        PMID: 34004101      PMCID: PMC8926149          DOI: 10.14341/probl12694

Source DB:  PubMed          Journal:  Probl Endokrinol (Mosk)        ISSN: 0375-9660


  51 in total

Review 1.  CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease.

Authors:  Thomas J Jentsch; Michael Pusch
Journal:  Physiol Rev       Date:  2018-07-01       Impact factor: 37.312

Review 2.  Insulin and oral agents for managing cystic fibrosis-related diabetes.

Authors:  Gary M Onady; Adrienne Stolfi
Journal:  Cochrane Database Syst Rev       Date:  2016-04-18

3.  CFTR silencing in pancreatic β-cells reveals a functional impact on glucose-stimulated insulin secretion and oxidative stress response.

Authors:  Thierry Ntimbane; Geneviève Mailhot; Schohraya Spahis; Remi Rabasa-Lhoret; Marie-Laure Kleme; Danielle Melloul; Emmanuelle Brochiero; Yves Berthiaume; Emile Levy
Journal:  Am J Physiol Endocrinol Metab       Date:  2015-12-01       Impact factor: 4.310

4.  Regulated Wnt/beta-catenin signaling sustains adult spermatogenesis in mice.

Authors:  Genevieve E Kerr; Julia C Young; Katja Horvay; Helen E Abud; Kate L Loveland
Journal:  Biol Reprod       Date:  2014-01-09       Impact factor: 4.285

5.  Increased NF-κB Activity and Decreased Wnt/β-Catenin Signaling Mediate Reduced Osteoblast Differentiation and Function in ΔF508 Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mice.

Authors:  Carole Le Henaff; Rafik Mansouri; Dominique Modrowski; Mylène Zarka; Valérie Geoffroy; Caroline Marty; Nadine Tarantino; Emmanuel Laplantine; Pierre J Marie
Journal:  J Biol Chem       Date:  2015-06-09       Impact factor: 5.157

Review 6.  Endocrine Disorders in Cystic Fibrosis.

Authors:  Scott M Blackman; Vin Tangpricha
Journal:  Pediatr Clin North Am       Date:  2016-08       Impact factor: 3.278

7.  Identification of the cystic fibrosis gene: chromosome walking and jumping.

Authors:  J M Rommens; M C Iannuzzi; B Kerem; M L Drumm; G Melmer; M Dean; R Rozmahel; J L Cole; D Kennedy; N Hidaka
Journal:  Science       Date:  1989-09-08       Impact factor: 47.728

8.  Cystic fibrosis transmembrane conductance regulator (CFTR) is expressed in human bone.

Authors:  Elizabeth F Shead; Charles S Haworth; Alison M Condliffe; Damian J McKeon; Mike A Scott; Juliet E Compston
Journal:  Thorax       Date:  2007-07       Impact factor: 9.139

9.  Defective CFTR-dependent CREB activation results in impaired spermatogenesis and azoospermia.

Authors:  Wen Ming Xu; Jing Chen; Hui Chen; Rui Ying Diao; Kin Lam Fok; Jian Da Dong; Ting Ting Sun; Wen Ying Chen; Mei Kuen Yu; Xiao Hu Zhang; Lai Ling Tsang; Ann Lau; Qi Xian Shi; Qing Hua Shi; Ping Bo Huang; Hsiao Chang Chan
Journal:  PLoS One       Date:  2011-05-09       Impact factor: 3.240

10.  Glucose-induced electrical activities and insulin secretion in pancreatic islet β-cells are modulated by CFTR.

Authors:  Jing Hui Guo; Hui Chen; Ye Chun Ruan; Xue Lian Zhang; Xiao Hu Zhang; Kin Lam Fok; Lai Ling Tsang; Mei Kuen Yu; Wen Qing Huang; Xiao Sun; Yiu Wa Chung; Xiaohua Jiang; Yoshiro Sohma; Hsiao Chang Chan
Journal:  Nat Commun       Date:  2014-07-15       Impact factor: 14.919

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