Expression and quantity dynamics of CK5+-immunopositive thymic epithelial cells of the subcapsular zone in rats of the early postnatal period after prenatal introduction of staphylococcal anatoxin.

Authors

  • N. A. Voloshin Zaporizhzhia State Medical University, Ukraine https://orcid.org/0000-0002-7162-1539
  • O. G. Kushch Zaporizhzhia State Medical University, Ukraine
  • E. O. Aravitskiy Zaporizhzhia State Medical University, Ukraine

DOI:

https://doi.org/10.26641/1997-9665.2018.4.24-30

Keywords:

thymus, CK5 -epithelioreticulocyte, staphylococcal anatoxin

Abstract

Background. Epithelioreticulocytes form the cellular basis of microenvironment in thymus, which regulate the processes of proliferation and differentiation of T-lymphocyte progenitor cells. In the cytoplasm of the epithelial cells cytokeratin-intermediate filaments are synthesized, who affect the mechanical stability and integrity of the epithelium. The influence of staphylococcal anatoxin on the morpho-functional state of the thymus, and particularly on the morphology and receptor composition of the thymic epithelial cells, is ambiguous and requires a more detailed study. Objective. to study the peculiarities of the distribution and expression of cytokeratin 5 by the epithelial cells of the thymus in norm and after prenatal introduction of staphylococcal anatoxin. Methods. The study was conducted on 144 white non-linear rats at 1, 2, 3, 5, 9, 14, 21, 30 days after birth. There were 3 groups of 48 rats: group 1 - intact; group 2 - experimental, who were intrauterine and intrafetally injected with 0,05 ml of staphylococcal anatoxin (1:10) on the 18th day of pregnancy; group 3 - controls, that were injected 0,05 ml of 0.9% NaCl. The standard sets of monoclonal mice antibody produced by Sigma-Aldrich (St. Louis, USA), and visualization system produced by Santa Cruz Biotechnology (California, USA) were used to study the receptor distribution to cytokeratin 5. Results. During the 30 days after birth in a group of rats, who had been introduced staphylococcal antigen, an increase in CK5 receptors expression was detected, with a peak within first three days and on the 14th day of life. The area occupied by CK5+-epithelioreticulocytes is significantly more than 1.5 times in rats of the experimental group from the 1st to the 9th day after birth, with a maximum on 1 day (29865 ± 3623 pix), decreasing further and almost reaching values of intact and control groups of rats up to the 30th day of observation. Conclusion. The revealed changes indicate a higher functional activity of epithelioreticulocytes, as microenvironmental cells, and their influence on the positive selection processes in the early postnatal period of ontogenesis in rats of the experimental group.

References

  1. Voloshin MA, Matveyshina TM. [Intrauterine effect of antigen as a factor contributing to the development of allergic-infectious diseases in newborns]. Bulletin of scientific research. 2012;3:111-4. Ukrainian.
  2. Voloshin NA, Medvedev AE, Vovchenko MB, Grigorieva EA, Popravko MI, Ivanov ME. [Histophysiological changes in organs after intrauterine antigen introduction]. In: [Scientific readings devoted to the 100th anniversary of the birthday of professor B.V.Aloshin; 2001 April; Kharkiv, Ukraine]. Kharkiv; 2001. p.4. Russian.
  3. Bal M, Ranjit M, Achary KG, Satapathy AK. Maternal filarial infection influences the development of regulatory T Cells in children from Infancy to early childhood. PLo S.Negl. Trop. Dis. 2016;10:452-6.
  4. Anderson G, Hare KJ, Jenkinson EJ. Specialisation of Thymic epithelial cells for positive selection of CD4+8+ thymocytes. Cell Mol. Biol. 2001;(1)47:119-27.
  5. Klein L, Hinterberger M, Wirnsberger G, Kyewski B. Antigen presentation in the thymus for positive selection and central tolerance induction. Nat Rev Immunol. 2009;9(12):833-44.
  6. Loginova NP, Chetvertnykh VA, Semchenko VV, Saydakova EV, Chemurzieva NV. [Features of cytokeratin (CK) 5 and 8 expression in thymus epithelial stromal cells and the number of TREC in peripheral T-lymphocytes in children with congenital heart defects]. Immunology. 2014;6:333-7. Russian.
  7. Volkov VP. [Functional immunomorphology of the thymus in the aspect of ontogenesis]. In: [XLVIII International Scientific and Practical Conference "Innovations in Science"; 2015 August 31; Novosibirsk, Russia]. SibAK; 2015. p.91. Russian.
  8. O'Neill KE, Bredenkamp N, Tischner C, Vaidya HJ, Stenhouse FH, Peddie C, Gaskell T. Foxn1 is dynamically regulated in thymic epithelial cells during embryogenesis and at the onset of thymicinvolution. PLoS One. 2016;3:76-9.
  9. Voloshin NA, Grigorieva EA, Kusch OG. [Intrauterine antigenic stimulation as a model for studying the morphogenesis of organs]. Morphological statements. 2006;1(2):57-9. Russian.
  10. Jaïdane H, Halouani A, Chakroun T, Sane F, Mokni M, Geenen V, Hober D. In-utero coxsackievirus B4 infection of the mouse thymus. Clin. Exp. Immunol. 2017;(3)187:399-407.
  11. Gorikov IN, Galigberov AA, Sukhov AN, Berendeeva VM, Tararaeva TV. [The morphological structure of the thymus and adrenal cortex in newborns from mothers who had adenoviral infection during pregnancy]. Actual problems of modern science. 2012;32:34-7. Russian.
  12. Gress RE, Deeks SG. Reduced thymus activity and infection prematurely age the immune system. J. Clin. Invest. 2009;(10)199:2884-7.

How to Cite

Voloshin, N. A., Kushch, O. G., & Aravitskiy, E. O. (2018). Expression and quantity dynamics of CK5+-immunopositive thymic epithelial cells of the subcapsular zone in rats of the early postnatal period after prenatal introduction of staphylococcal anatoxin. Морфологія / Morphologia / Morfologìâ, 12(4), 24–30. https://doi.org/10.26641/1997-9665.2018.4.24-30

Issue

Section

Статті