open access

Vol 55, No 1 (2017)
Original paper
Submitted: 2017-03-23
Accepted: 2017-03-29
Published online: 2017-03-31
Get Citation

Ultrastructural characteristics of myenteric plexus in patients with colorectal cancer

Agata Zauszkiewicz-Pawlak, Janusz Godlewski, Przemyslaw Kwiatkowski, Zbigniew Kmiec
·
Pubmed: 28509311
·
Folia Histochem Cytobiol 2017;55(1):6-10.

open access

Vol 55, No 1 (2017)
ORIGINAL PAPERS
Submitted: 2017-03-23
Accepted: 2017-03-29
Published online: 2017-03-31

Abstract

Introduction. It have been found previously that colorectal cancer (CRC) is accompanied by atrophy of myenteric plexuses (MPs) localized close to the tumor. The aim of the study was to compare ultrastructure of MPs localized in the unchanged part of the colon wall distant to CRC tumor with the ultrastructure of MPs in the vicinity of CRC tumor.

Material and methods. The present study was conducted using post-operative material derived from 11 patients with CRC. Samples of colon wall were taken from the margin of cancer invasion and from a macroscopically unchanged segment of the large intestine, immediately fixed and processed according to the standard protocol for transmission electron microscopy studies.

Results. In the MPs localized in the control part of colon wall the presence of numerous unmyelinated axons and cell bodies of neurons, interstitial cells of Cajal and enteroglial cells were observed. As compared to control samples, in the MPs located close to the tumor invasion, expansion of the extracellular matrix and myelin-like structures accompanying some nerve fibers were found. The appearance of mast and plasma cells was observed within MPs in the vicinity of CRC tumor. Sporadically, apoptotic cells were present inside the MPs.

Conclusions. The presence of myelin-like structures and apoptotic cells within MPs located close to tumor invasion suggests that atrophy of MPs may be caused by factors released from CRC tumor.

Abstract

Introduction. It have been found previously that colorectal cancer (CRC) is accompanied by atrophy of myenteric plexuses (MPs) localized close to the tumor. The aim of the study was to compare ultrastructure of MPs localized in the unchanged part of the colon wall distant to CRC tumor with the ultrastructure of MPs in the vicinity of CRC tumor.

Material and methods. The present study was conducted using post-operative material derived from 11 patients with CRC. Samples of colon wall were taken from the margin of cancer invasion and from a macroscopically unchanged segment of the large intestine, immediately fixed and processed according to the standard protocol for transmission electron microscopy studies.

Results. In the MPs localized in the control part of colon wall the presence of numerous unmyelinated axons and cell bodies of neurons, interstitial cells of Cajal and enteroglial cells were observed. As compared to control samples, in the MPs located close to the tumor invasion, expansion of the extracellular matrix and myelin-like structures accompanying some nerve fibers were found. The appearance of mast and plasma cells was observed within MPs in the vicinity of CRC tumor. Sporadically, apoptotic cells were present inside the MPs.

Conclusions. The presence of myelin-like structures and apoptotic cells within MPs located close to tumor invasion suggests that atrophy of MPs may be caused by factors released from CRC tumor.

Get Citation

Keywords

colorectal carcinoma; enteric nervous system; myenteric plexus atrophy; apoptosis; Cajal cells; electron microscopy

About this article
Title

Ultrastructural characteristics of myenteric plexus in patients with colorectal cancer

Journal

Folia Histochemica et Cytobiologica

Issue

Vol 55, No 1 (2017)

Article type

Original paper

Pages

6-10

Published online

2017-03-31

Page views

1742

Article views/downloads

1652

DOI

10.5603/FHC.a2017.0003

Pubmed

28509311

Bibliographic record

Folia Histochem Cytobiol 2017;55(1):6-10.

Keywords

colorectal carcinoma
enteric nervous system
myenteric plexus atrophy
apoptosis
Cajal cells
electron microscopy

Authors

Agata Zauszkiewicz-Pawlak
Janusz Godlewski
Przemyslaw Kwiatkowski
Zbigniew Kmiec

References (21)
  1. Timmermans JP, Adriaensen D, Cornelissen W, et al. Structural organization and neuropeptide distribution in the mammalian enteric nervous system, with special attention to those components involved in mucosal reflexes. Comp Biochem Physiol A Physiol. 1997; 118(2): 331–340.
  2. Timmermans JP, Adriaensen D. Gastrointestinal mechanosensors: analysis of multiple stimuli may require complex sensors. Neurogastroenterol Motil. 2008; 20(1): 4–7.
  3. Wedel T, Roblick U, Gleiss J, et al. Organization of the enteric nervous system in the human colon demonstrated by wholemount immunohistochemistry with special reference to the submucous plexus. Ann Anat. 1999; 181(4): 327–337.
  4. Furness JB, Bornstein JC, Trussell DC. Shapes of nerve cells in the myenteric plexus of the guinea-pig small intestine revealed by the intracellular injection of dye. Cell Tissue Res. 1988; 254(3): 561–571.
  5. Stach W. A revised morphological classification of neurons in the enteric nervous system. Kluwer Academic Publishers, Lancaster, UK 1989.
  6. Furness JB. The enteric nervous system and neurogastroenterology. Nat Rev Gastroenterol Hepatol. 2012; 9(5): 286–294.
  7. Kurahashi M, Zheng H, Dwyer L, et al. A functional role for the 'fibroblast-like cells' in gastrointestinal smooth muscles. J Physiol. 2011; 589(Pt 3): 697–710.
  8. Cobine CA, Hennig GW, Kurahashi M, et al. Relationship between interstitial cells of Cajal, fibroblast-like cells and inhibitory motor nerves in the internal anal sphincter. Cell Tissue Res. 2011; 344(1): 17–30.
  9. Ochoa-Cortes F, Turco F, Linan-Rico A, et al. Enteric glial cells: a new frontier in neurogastroenterology and clinical target for inflammatory bowel diseases. Inflamm Bowel Dis. 2016; 22(2): 433–449.
  10. Rumessen JJ, Vanderwinden JM, Horn T. Crohn's disease: ultrastructure of interstitial cells in colonic myenteric plexus. Cell Tissue Res. 2011; 344(3): 471–479.
  11. Rumessen JJ, Vanderwinden JM, Horn T, et al. Ulcerative colitis: ultrastructure of interstitial cells in myenteric plexus. Ultrastruct Pathol. 2010; 34(5): 279–287.
  12. Godlewski J, Pidsudko Z. Characteristic of galaninergic components of the enteric nervous system in the cancer invasion of human large intestine. Ann Anat. 2012; 194(4): 368–372.
  13. Godlewski J. Morphological changes in the enteric nervous system caused by carcinoma of the human large intestine. Folia Histochem Cytobiol. 2010; 48(1): 157–162.
  14. Lebouvier T, Neunlist M, Bruley des Varannes S, et al. Colonic biopsies to assess the neuropathology of Parkinson's disease and its relationship with symptoms. PLoS One. 2010; 5(9): e12728.
  15. Kwiatkowski P, Godlewski J, Kieżun J, et al. Colorectal cancer patients exhibit increased levels of galanin in serum and colon tissues. Oncol Lett. 2016; 12(5): 3323–3329.
  16. Kozlowska A, Kwiatkowski P, Oponowicz A, et al. Myenteric plexuses atrophy in the vicinity of colorectal cancer tissue is not caused by apoptosis or necrosis. Folia Histochem Cytobiol. 2016; 54(2): 99–107.
  17. Saggu SK, Chotaliya HP, Blumbergs PC, et al. Wallerian-like axonal degeneration in the optic nerve after excitotoxic retinal insult: an ultrastructural study. BMC Neurosci. 2010; 11: 97.
  18. Schuettauf F, Rejdak R, Walski M, et al. Retinal neurodegeneration in the DBA/2J mouse-a model for ocular hypertension. Acta Neuropathol. 2004; 107(4): 352–358.
  19. Skalska J, Frontczak-Baniewicz M, Strużyńska L. Synaptic degeneration in rat brain after prolonged oral exposure to silver nanoparticles. Neurotoxicology. 2015; 46: 145–154.
  20. Murakoshi M, Osamura Y, Watanabe K. Mitochondrial alterations in aged rat adrenal cortical cells. Tokai J Exp Clin Med. 1985; 10(5): 531–536.
  21. Wedel T, Holschneider AM, Krammer HJ. Ultrastructural features of nerve fascicles and basal lamina abnormalities in Hirschsprung's disease. Eur J Pediatr Surg. 1999; 9(2): 75–82.

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., ul. Świętokrzyska 73, 80–180 Gdańsk

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