Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Dec 18;46(12):14259-14269.
doi: 10.3390/cimb46120854.

Immunolocalization of Na(+)-Dependent Glucose Co-Transporters in Chicken Kidneys in Norm and During T-2 Mycotoxicosis (Primary Study)

Affiliations

Immunolocalization of Na(+)-Dependent Glucose Co-Transporters in Chicken Kidneys in Norm and During T-2 Mycotoxicosis (Primary Study)

Cristin Allmang et al. Curr Issues Mol Biol. .

Abstract

The kidney plays an essential role in the proper homeostasis of glucose. In the kidney, glucose transport is carried out across cell membranes by two families of glucose transporters-facilitated diffusion glucose transporters (GLUTs) and Na(+)-dependent glucose co-transporters (SGLT family). Among the transporters, sodium-dependent glucose co-transporters play a major role in the kidney's ability to reabsorb glucose. Although the localization of glucose transporters has been extensively studied in mammals, there are still knowledge gaps regarding the localization of SGLTs in birds. The aim of this research was to conduct a comparative study of the immunolocalization of the sodium-dependent glucose co-transporters SGLT1 and SGLT2 in the kidneys of healthy and T-2-mycotoxicated chickens. Immunohistochemical staining was carried out using the polyclonal primary antibodies SGLT1 and SGLT2 (Abcam, UK) in kidney tissue derived from seven healthy and seven T-2-mycotoxicated 7-day-old female layer-type Ross chickens (Gallus gallus domesticus). The sections were stained using an immunohistochemistry kit (Abcam, UK). In the kidneys of the healthy birds, strong staining of SGLT1 and SGLT2 was observed in the cytoplasm of the epithelial cells of the proximal straight and convoluted tubules. In the kidneys of the birds of the T-2 toxin group, weak expression of SGLT1 and SGLT2 with morphological changes occurred, indicating reduced glucose transport in the urinary system during T-2 mycotoxicosis.

Keywords: chicken; immunohistochemistry; mycotoxicosis; sodium-dependent glucose co-transporter.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflicts of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

Figures

Figure 1
Figure 1
Na(+)-dependent glucose co-transporter 2 transmembrane transport in bird kidneys. SGLT2 = Na(+)-dependent glucose co-transporter 2; GLUT2 = facilitative glucose transport.
Figure 2
Figure 2
Normal kidney morphology of a 7-day-old chicken: proximal (arrowheads) and distal tubules (arrows) in the cortex of the kidney. Hematoxylin and eosin. Magnification 400×, scale bar 100 µm.
Figure 3
Figure 3
Immunolocalization of the sodium-dependent glucose co-transporter-1 (SGLT1) in kidney tissue (a) in healthy 7-day-old chickens; note the strong expression of SGLT1 in the apical part of the epithelial cells of renal proximal tubules (arrowheads). Magnification 400×, scale bar 50 µm; (b) damaged brush border membranes of proximal tubule’s epithelial cells in intoxicated chicken (arrows). Magnification 400×, scale bar 50 µm.
Figure 4
Figure 4
Immunolocalization of sodium-dependent glucose co-transporter-2 (SGLT2) in (a) strongly stained proximal tubules (arrowheads) of healthy chicken kidney and weakly stained distal tubules (arrows) is observed. Magnification 400×, scale bar 50 µm; (b) the pale staining of proximal renal tubules (arrows) of intoxicated bird group is observed. Magnification 400×, scale bar 50 µm.
Figure 5
Figure 5
SGLT2 in healthy 7-day-old chicken kidneys. Note the unstained collecting ducts (arrows); immunohistochemistry (IHC) magnification 400×, scale bar 50 µm.

Similar articles

References

    1. Hruby V.J. In: Molecular and Cellular Endocrinology. Bittar E., Bittar N., editors. Volume 10. JAI Press Inc.; Greenwhich, CT, USA: 1997. pp. 387–401.
    1. Mota M., Mota E., Dinu I.R. In: Treatment of Type 2 Diabetes. Croniger C., editor. IntechOpen; Rijeka, Crotaia: 2015. pp. 13–17. Chapter 1.
    1. König H.E., Korbel R., Liebich H.G. Avian Anatomy Textbook and Colour Atlas. Volume 2. 5m Publishing; Sheffield, UK: 2016. pp. 131–133.
    1. Vallon V., Thomson S.C. Renal Function in Diabetic Disease Models: The Tubular System in the Pathophysiology of the Diabetic Kidney. Annu. Rev. Physiol. 2012;74:351–375. doi: 10.1146/annurev-physiol-020911-153333. - DOI - PMC - PubMed
    1. Haas B., Eckstein N., Pfeifer V., Mayer P., Hass M.D.S. Efficacy, Safety and Regulatory Status of SGLT2 Inhibitors: Focus on Canagliflozin. Nutr. Diabetes. 2014;4:e143. doi: 10.1038/nutd.2014.40. - DOI - PMC - PubMed

LinkOut - more resources