open access

Vol 78, No 1 (2019)
Original article
Submitted: 2018-03-28
Accepted: 2018-05-30
Published online: 2018-07-17
Get Citation

Distribution of epidermal growth factor receptor, bone morphogenetic protein-2, and p53 in kidney of healthy newborn, adult and old highland-plateau yaks

T. Wang1, Y. Cui1, P. Liu1, J. He1, Q. Zhang1
·
Pubmed: 30106465
·
Folia Morphol 2019;78(1):114-123.
Affiliations
  1. Faculty of Veterinary Medicine, Gansu Agricultural University, Lanzhou, China

open access

Vol 78, No 1 (2019)
ORIGINAL ARTICLES
Submitted: 2018-03-28
Accepted: 2018-05-30
Published online: 2018-07-17

Abstract

Background: Kidney has long been thought to be a body’s largest organ of elimination for maintaining acid-base balance. In recent years, the research on kidneys has mainly focused on the structural characteristics of the kidney of single age group animals. In this paper we used histological and immunohistochemical methods to observe and compare the structure characteristics of yak kidney and the expression of epidermal growth factor receptor (EGFR), bone morphogenetic protein-2 (BMP-2) and p53 in the kidney of yaks of three different age groups. The aim of the study was to investigate histological characteristics of age-related chan- ges in the kidney of yak and expression and localisation of kidney-related factors. 

Materials and methods: Fifteen healthy male and female yaks from highland plateaus (three groups: newborn, adult and old yaks, n = 5 per group). Histo- logical methods were used to compare the relevant characteristics of the kidney of yaks. The immunohistochemistry method was used to observe the expression and localisation of EGFR, BMP-2, and p53 of the kidney of different ages, and the optical density value was measured and analysed by using image analysis software.

Results: This is an overall observation of the kidney tissue section, which includes the surface of the renal capsule and the internal parenchyma. In the renal parenchyma, there are renal corpuscles, renal tubules. The internal substance included cortex and medulla, which were bounded by the arched artery. In the cortex, there were renal corpuscles, convoluted part of renal tubules (proximal convoluted tubule and distal convoluted tubule) and collecting tubules. The medulla included straight parts of renal tubules (proximal straight tubule and distal straight tubule), thin segments and collecting tubules. It was observed that the organisational structure of the kidney of yaks did not change with age, but the degree of development of the internal structure (glomeruli, renal tubules and collecting tubules) of the kidney changed with age. Immunohistochemical results demonstrated that EGFR and BMP-2-positive reaction in the newborn group was mainly distributed in the proximal tubule epithelial cells, and widely distributed in the adult and old groups. However, the p53-positive reaction was widely distributed in the newborn, adult and old groups. 

Conclusions: The results revealed that the kidney structure tended to be com- pleted with age, and the function of the kidney gradually improved. EGFR and BMP-2 had the effect of promoting kidney development. However, p53 had been widely distributed in the newborn kidney of the yaks. It is suggested that p53 had been involved in cell migration and metabolic differentiation and self-renewal in the new stage. 

Abstract

Background: Kidney has long been thought to be a body’s largest organ of elimination for maintaining acid-base balance. In recent years, the research on kidneys has mainly focused on the structural characteristics of the kidney of single age group animals. In this paper we used histological and immunohistochemical methods to observe and compare the structure characteristics of yak kidney and the expression of epidermal growth factor receptor (EGFR), bone morphogenetic protein-2 (BMP-2) and p53 in the kidney of yaks of three different age groups. The aim of the study was to investigate histological characteristics of age-related chan- ges in the kidney of yak and expression and localisation of kidney-related factors. 

Materials and methods: Fifteen healthy male and female yaks from highland plateaus (three groups: newborn, adult and old yaks, n = 5 per group). Histo- logical methods were used to compare the relevant characteristics of the kidney of yaks. The immunohistochemistry method was used to observe the expression and localisation of EGFR, BMP-2, and p53 of the kidney of different ages, and the optical density value was measured and analysed by using image analysis software.

Results: This is an overall observation of the kidney tissue section, which includes the surface of the renal capsule and the internal parenchyma. In the renal parenchyma, there are renal corpuscles, renal tubules. The internal substance included cortex and medulla, which were bounded by the arched artery. In the cortex, there were renal corpuscles, convoluted part of renal tubules (proximal convoluted tubule and distal convoluted tubule) and collecting tubules. The medulla included straight parts of renal tubules (proximal straight tubule and distal straight tubule), thin segments and collecting tubules. It was observed that the organisational structure of the kidney of yaks did not change with age, but the degree of development of the internal structure (glomeruli, renal tubules and collecting tubules) of the kidney changed with age. Immunohistochemical results demonstrated that EGFR and BMP-2-positive reaction in the newborn group was mainly distributed in the proximal tubule epithelial cells, and widely distributed in the adult and old groups. However, the p53-positive reaction was widely distributed in the newborn, adult and old groups. 

Conclusions: The results revealed that the kidney structure tended to be com- pleted with age, and the function of the kidney gradually improved. EGFR and BMP-2 had the effect of promoting kidney development. However, p53 had been widely distributed in the newborn kidney of the yaks. It is suggested that p53 had been involved in cell migration and metabolic differentiation and self-renewal in the new stage. 

Get Citation

Keywords

bone morphogenetic protein-2; epidermal growth factor receptor; kidney; tumour suppressive gene p53; yak

About this article
Title

Distribution of epidermal growth factor receptor, bone morphogenetic protein-2, and p53 in kidney of healthy newborn, adult and old highland-plateau yaks

Journal

Folia Morphologica

Issue

Vol 78, No 1 (2019)

Article type

Original article

Pages

114-123

Published online

2018-07-17

Page views

1973

Article views/downloads

1003

DOI

10.5603/FM.a2018.0067

Pubmed

30106465

Bibliographic record

Folia Morphol 2019;78(1):114-123.

Keywords

bone morphogenetic protein-2
epidermal growth factor receptor
kidney
tumour suppressive gene p53
yak

Authors

T. Wang
Y. Cui
P. Liu
J. He
Q. Zhang

References (40)
  1. Attisano L, Wrana JL. Mads and Smads in TGF beta signalling. Curr Opin Cell Biol. 1998; 10(2): 188–194.
  2. Bauchet AL, Masson R, Guffroy M, et al. Immunohistochemical identification of kidney nephron segments in the dog, rat, mouse, and cynomolgus monkey. Toxicol Pathol. 2011; 39(7): 1115–1128.
  3. Baserga M, Hale MA, Ke X, et al. Uteroplacental insufficiency increases p53 phosphorylation without triggering the p53-MDM2 functional circuit response in the IUGR rat kidney. Am J Physiol Regul Integr Comp Physiol. 2006; 291(2): R412–R418.
  4. Ciardiello F, Tortora G. EGFR antagonists in cancer treatment. N Engl J Med. 2008; 358(11): 1160–1174.
  5. El-Dahr S, Hilliard S, Aboudehen K, et al. The MDM2-p53 pathway: multiple roles in kidney development. Pediatr Nephrol. 2014; 29(4): 621–627.
  6. Gattone VH, Sherman DA, Hinton DA, et al. Epidermal growth factor in the neonatal mouse salivary gland and kidney. Biol Neonate. 1992; 61(1): 54–67.
  7. Gekle M. Kidney and aging: a narrative review. Exp Gerontol. 2017; 87(Pt B): 153–155.
  8. Gesualdo L, Di Paolo S, Calabró A, et al. Expression of epidermal growth factor and its receptor in normal and diseased human kidney: an immunohistochemical and in situ hybridization study. Kidney Int. 1996; 49(3): 656–665.
  9. Gottlieb E, Vousden KH. p53 regulation of metabolic pathways. Cold Spring Harb Perspect Biol. 2010; 2(4): a001040.
  10. Gu W, Yang L, Wang S, et al. Generation and application of a novel InsP(3)R(1) mono-antibody from mouse. J Immunoassay Immunochem. 2015; 36(5): 487–495.
  11. Harris RC. Potential physiologic roles for epidermal growth factor in the kidney. Am J Kidney Dis. 1991; 17(6): 627–630.
  12. He X, Xie Z, Dong Q, et al. Dynamic p53 protein expression and phosphorylation in the kidneys of rats that experienced intrauterine growth restriction. Ren Fail. 2015; 37(5): 896–902.
  13. He Y, Yu S, Hu J, et al. Changes in the Anatomic and Microscopic Structure and the Expression of HIF-1α and VEGF of the Yak Heart with Aging and Hypoxia. PLoS One. 2016; 11(2): e0149947.
  14. Heldin CH, Miyazono K, ten Dijke P. TGF-beta signalling from cell membrane to nucleus through SMAD proteins. Nature. 1997; 390(6659): 465–471.
  15. Hilliard S, Aboudehen K, Yao X, et al. Tight regulation of p53 activity by Mdm2 is required for ureteric bud growth and branching. Dev Biol. 2011; 353(2): 354–366.
  16. Hogan BL. Bone morphogenetic proteins: multifunctional regulators of vertebrate development. Genes Dev. 1996; 10(13): 1580–1594.
  17. Hogan BL. Bone morphogenetic proteins in development. Curr Opin Genet Dev. 1996; 6(4): 432–438.
  18. Hommos MS, Glassock RJ, Rule AD. Structural and Functional Changes in Human Kidneys with Healthy Aging. J Am Soc Nephrol. 2017; 28(10): 2838–2844.
  19. Iwasaki S, Tsuruoka N, Hattori A, et al. Distribution and characterization of specific cellular binding proteins for bone morphogenetic protein-2. J Biol Chem. 1995; 270(10): 5476–5482.
  20. Jung JY, Song JH, Li C, et al. Expression of epidermal growth factor in the developing rat kidney. Am J Physiol Renal Physiol. 2005; 288(1): F227–F235.
  21. Kozma C. Anatomy, Physiology, and Biochemistry of the Rabbit. The biology of the laboratory rabbit. 1974; 12(1): 55–58.
  22. Kretzschmar M, Doody J, Massagué J. Opposing BMP and EGF signalling pathways converge on the TGF-beta family mediator Smad1. Nature. 1997; 389(6651): 618–622.
  23. Li Y, Wei Qw, Feng Jg, et al. Expression of bone morphogenetic protein 2, 4, and related components of the BMP signaling pathway in the mouse uterus during the estrous cycle. J Zhejiang Univ Sci B. 2014; 15(7): 601–610.
  24. Liebelt A. Unique Features of Anatomy, Histology, and Ultrastructure Kidney, Mouse. Urinary System. Springer Berlin Heidelberg. 1998: 37–57.
  25. Liu P, Yu S, Cui Y, et al. Cloning of HSP90, expression and localization of HSP70/90 in different tissues including lactating/non-lactating yak (Bos grunniens) breast tissue. PLoS One. 2017; 12(7): e0179321.
  26. Lu ZQ, Peng KM, Zhang JB, et al. Histological Study on the African White Rhinoceros Kidney. Proceedings of the 17th Academic Symposium on Animal Anatomy and Tissue Embryology Branch of Chinese Association of Animal Sience and Veterinary Medicine. 2010: 285–288.
  27. Massagué J. TGFbeta signaling: receptors, transducers, and Mad proteins. Cell. 1996; 85(7): 947–950.
  28. McBride J. Embryology, anatomy, and histology of the kidney. The Kidney. 2016: 1–18.
  29. Molchadsky A, Rivlin N, Brosh R, et al. p53 is balancing development, differentiation and de-differentiation to assure cancer prevention. Carcinogenesis. 2010; 31(9): 1501–1508.
  30. Pastore S, Mascia F, Mariani V, et al. The epidermal growth factor receptor system in skin repair and inflammation. J Invest Dermatol. 2008; 128(6): 1365–1374.
  31. Schoppy DW, Ruzankina Y, Brown EJ. Removing all obstacles: a critical role for p53 in promoting tissue renewal. Cell Cycle. 2010; 9(7): 1313–1319.
  32. Seely JC. A brief review of kidney development, maturation, developmental abnormalities, and drug toxicity: juvenile animal relevancy. J Toxicol Pathol. 2017; 30(2): 125–133.
  33. Tang J, Liu Na, Zhuang S. Role of epidermal growth factor receptor in acute and chronic kidney injury. Kidney Int. 2013; 83(5): 804–810.
  34. Tauchi H, Tsuboi K, Okutomi J. Age changes in the human kidney of the different races. Gerontologia. 1971; 17(2): 87–97.
  35. Tumelty KE, Higginson-Scott N, Fan X, et al. Identification of direct negative cross-talk between the SLIT2 and bone morphogenetic protein-Gremlin signaling pathways. J Biol Chem. 2018; 293(9): 3039–3055.
  36. Wang WH, Chen HT. Studies on Comparative Histology of the Kidneys in Bactrian Camels (Camelus bactrianus). Journal of Lanzhou University. 2000; 36(4): 73–78.
  37. Xi Y, Shao F, Bai XY, et al. Changes in the expression of the Toll-like receptor system in the aging rat kidneys. PLoS One. 2014; 9(5): e96351.
  38. Yang B, Yu S, Cui Y, et al. Morphological analysis of the lung of neonatal yak. Anat Histol Embryol. 2010; 39(2): 138–151.
  39. Zhang H, Bradley A. Mice deficient for BMP2 are nonviable and have defects in amnion/chorion and cardiac development. Development. 1996; 122(10): 2977–2986.
  40. Zhang Q, Yang K, Huang Y, et al. Distribution of T-cell markers CD4 and CD8α in lymphoid organs of healthy newborn, juvenile, and adult highland-plateau yaks. Am J Vet Res. 2017; 78(5): 609–617.

Regulations

Important: This website uses cookies. More >>

The cookies allow us to identify your computer and find out details about your last visit. They remembering whether you've visited the site before, so that you remain logged in - or to help us work out how many new website visitors we get each month. Most internet browsers accept cookies automatically, but you can change the settings of your browser to erase cookies or prevent automatic acceptance if you prefer.

By VM Media Group sp. z o.o., Grupa Via Medica, Świętokrzyska 73, 80–180 Gdańsk, Poland

tel.: +48 58 320 94 94, faks: +48 58 320 94 60, e-mail: viamedica@viamedica.pl