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Animals : an open access journal from MDPI2022; 12(10); 1324; doi: 10.3390/ani12101324

Comparative Histology of C Thyrocytes in Four Domestic Animal Species: Dog, Pig, Horse, and Cattle.

Abstract: The number, morphology, and distribution of C thyrocytes within the thyroid gland vary among species; however, studies in domestic animals are limited. In this study we compared the morphology, distribution pattern, and percentage of C thyrocytes in four domestic species: dogs, pigs, horses, and cattle. Eighty thyroid glands, 20 per species, were examined. C thyrocytes were visualized immunohistochemically with anti-calcitonin rabbit polyclonal antibody alone and combined with the periodic acid Schiff method to simultaneously visualize C thyrocytes with the basement membranes of thyroid follicles. C thyrocyte morphology varied considerably between species, from oval- (dogs) and spindle-shaped (pigs) to polymorphic (cattle and horses). Bovine C thyrocytes demonstrated cytoplasmic protrusion. C thyrocytes were located intrafolliculary (all species), epifollicularly (dogs, horses, cattle), or interfolicularly (cattle). Most porcine and bovine C thyrocytes existed individually whereas canine C thyrocytes usually formed clusters. In horses, they tended to form groups of various shapes and sizes or even rims encompassing whole follicles. In all species, the number of C thyrocyte profiles increased from the periphery to the central area of the thyroid lobe. The mean total fraction of C thyrocytes in the superficial, intermediate, and central areas were as follows: 2.55%, 8.43%, and 12.48% in dogs; 3.81%, 7.66%, and 10.79% in pigs; 1.55%, 7.44%, and 8.87% in horses; and 2.62%, 10.75%, and 12.96% in cattle. No statistical differences in the total number of C thyrocyte profiles were observed among species (8.87% in dogs, 8.58% in cattle, 7.98% in pigs, and 5.83% in horses). Our results indicated that the studied species displayed their own morphological characteristics and distribution pattern of C thyrocytes; however, total numbers of C thyrocyte profiles and their localization within the thyroid lobe are comparable.
Publication Date: 2022-05-23 PubMed ID: 35625170PubMed Central: PMC9137929DOI: 10.3390/ani12101324Google Scholar: Lookup
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Summary

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This research explores the differences in number, shape, and distribution of C thyrocytes (a type of cell in the thyroid gland) among domestic animals: dogs, pigs, horses, and cattle. The study finds distinct variations, yet comparable overall quantities and placement within the thyroid gland; suggesting that these species exhibit unique morphological traits despite having similar C thyrocyte profiles.

Experimental Method

  • Researchers analysed eighty thyroid glands, with 20 samples from each of the four species
  • The visualization of C thyrocytes was carried out using immunohistochemical processes with anti-calcitonin rabbit polyclonal antibody
  • The periodic acid Schiff method was also implemented to concurrently observe C thyrocytes alongside the basement membranes of thyroid follicles

Key Findings

  • Shape of C thyrocytes differed among the studied species: dogs had oval-shaped thyrocytes; pigs had spindle-shaped thyrocytes; while those of cattle and horses were polymorphic
  • C thyrocytes were found in three location categories: intrafollicular (across all species), epifollicular (in dogs, horses, cattle), and interfolicular (only in cattle)
  • Dogs’ C thyrocytes typically formed clusters, while pigs and cows usually exhibited individual thyrocytes. Horses, on the other hand, demonstrated groupings of different shapes and sizes, and sometimes even rims that encompassed entire follicles
  • In every species, the quantity of C thyrocyte profiles increased from the periphery to the center of the thyroid lobe
  • The total fraction of C thyrocytes varied within the superficial, intermediate, and central areas of the thyroid lobe

Implications and Conclusions

  • The study’s results signify that whilst different species exhibit distinct morphological characteristics and C thyrocyte distribution patterns, the overall quantities of C thyrocyte profiles and their placement within the thyroid lobe were comparable
  • This research contributes valuable insights to the limited understanding of C thyrocytes’s histoarchitecture in domestic animals, which can potentially support further investigations into species-specific treatments and interventions regarding thyroid conditions

Cite This Article

APA
Sokołowska J, Cywińska A, Puchalska M. (2022). Comparative Histology of C Thyrocytes in Four Domestic Animal Species: Dog, Pig, Horse, and Cattle. Animals (Basel), 12(10), 1324. https://doi.org/10.3390/ani12101324

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 12
Issue: 10
PII: 1324

Researcher Affiliations

Sokołowska, Justyna
  • Department of Morphological Sciences, Institute of Veterinary Medicine, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland.
Cywińska, Anna
  • Department of Basic and Preclinical Sciences, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University in Toruń, Lwowska 1, 87-100 Toruń, Poland.
Puchalska, Martyna
  • Department of Food Hygiene and Public Health Protection, Institute of Veterinary Medicine, Warsaw University of Life Sciences-SGGW, Nowoursynowska 159, 02-776 Warsaw, Poland.

Conflict of Interest Statement

The authors declare no conflict of interest.

References

This article includes 42 references
  1. Fernández-Santos J.M., Morillo-Bernal J., García-Marín R., Utrilla J.C., Martín-Lacave I.. Paracrine regulation of thyroid-hormone synthesis by C cells. In: Agrawal N.K., editor. Thyroid Hormone. IntechOpen; London, UK: 2012. pp. 51–84.
    doi: 10.5772/46178google scholar: lookup
  2. Kameda Y. Cellular and molecular events on the development of mammalian thyroid C cells.. Dev Dyn 2016 Mar;245(3):323-41.
    doi: 10.1002/dvdy.24377pubmed: 26661795google scholar: lookup
  3. Wolfe HJ, Voelkel EF, Tashjian AH Jr. Distribution of calcitonin-containing cells in the normal adult human thyroid gland: a correlation of morphology with peptide content.. J Clin Endocrinol Metab 1974 Apr;38(4):688-94.
    doi: 10.1210/jcem-38-4-688pubmed: 4132222google scholar: lookup
  4. Sawicki B.. Morphology and histochemistry of thyroid gland C cells of young and adult guinea pigs. Acta Theriol 1975;20:281–296.
    doi: 10.4098/AT.arch.75-25google scholar: lookup
  5. Sawicki B., Kuczyński M.. Morphological studies on the C cells of the thyroid of certain rodents. Acta Theriol 1977;22:251–260.
    doi: 10.4098/AT.arch.77-20google scholar: lookup
  6. Zabel M, Schäfer H, Surdyk J, Biela-Jacek I. Immunocytochemical studies on parafollicular cells of various mammals.. Acta Anat (Basel) 1988;131(3):222-6.
    doi: 10.1159/000146518pubmed: 3259783google scholar: lookup
  7. Kameda Y. Immunohistochemical study of c cell follicles in dog thyroid glands.. Anat Rec 1982 Sep;204(1):55-60.
    doi: 10.1002/ar.1092040108pubmed: 6756211google scholar: lookup
  8. Kameda Y, Ikeda A. Immunohistochemical study of the C-cell complex of dog thyroid glands with reference to the reactions of calcitonin, C-thyroglobulin and 19S thyroglobulin.. Cell Tissue Res 1980;208(3):405-15.
    doi: 10.1007/BF00233873pubmed: 6994887google scholar: lookup
  9. Rost MC, Rost FW. Storage granules of thyroid C cells in the dog: a cytochemical and ultrastructural study, in relation to the masked metachromasia reaction.. Histochem J 1975 Jul;7(4):307-20.
    doi: 10.1007/BF01007016pubmed: 50304google scholar: lookup
  10. Tsuchiya T, Shiomura Y, Suzuki K, Nagai H, Tamate H. Immunocytochemical study on the C cells in pig thyroid glands.. Acta Anat (Basel) 1984;120(3):138-41.
    doi: 10.1159/000145907pubmed: 6516770google scholar: lookup
  11. Young BA, Care AD, Duncan T. Some observations on the light cells of the thyroid gland of the pig in relation to thyrocalcitonin production.. J Anat 1968 Jan;102(Pt 2):275-88.
    pmc: PMC1231315pubmed: 5643843
  12. Okada HM, Matsukawa K, Ohgiya N, Yokota H, Taniyama H, Yuasa A. Immunohistochemical demonstration of parafollicular (C) cells in sheep thyroid and parathyroid glands.. Nihon Juigaku Zasshi 1990 Aug;52(4):879-82.
    doi: 10.1292/jvms1939.52.879pubmed: 2202848google scholar: lookup
  13. Sokolowska J, Berczynska J, Poweska A, Rygiel D, Olbrych K, Urbanska K. Immunohistochemical characteristic of C cells in European bison thyroid gland.. Folia Histochem Cytobiol 2018;56(4):222-230.
    doi: 10.5603/FHC.a2018.0024pubmed: 30565206google scholar: lookup
  14. Yanai T, Tateyama S, Nosaka D, Ashizawa H. Some observations on the parafollicular (C) cells in the equine thyroid.. Nihon Juigaku Zasshi 1982 Jun;44(3):511-6.
    doi: 10.1292/jvms1939.44.511pubmed: 7132021google scholar: lookup
  15. Yoshikawa H., Ueki H., Muranaka M., Oyamada T., Yoshikawa T.. Distribution of C cells in thyroids and association with age and sex in racing horses. J. Equine Sci. 2001;12:39–45.
    doi: 10.1294/jes.12.39google scholar: lookup
  16. Kameda Y, Shigemoto H, Ikeda A. Development and cytodifferentiation of C cell complexes in dog fetal thyroids. An immunohistochemical study using anti-calcitonin, anti-C-thyroglobulin and anti-19S thyroglobulin antisera.. Cell Tissue Res 1980;206(3):403-15.
    doi: 10.1007/BF00237970pubmed: 6993005google scholar: lookup
  17. Leblanc B, Parodi AL, Lagadic M, Hurtrel M, Jobit C. Immunocytochemistry of canine thyroid tumors.. Vet Pathol 1991 Sep;28(5):370-80.
    doi: 10.1177/030098589102800504pubmed: 1750162google scholar: lookup
  18. Nilsson M, Williams D. On the Origin of Cells and Derivation of Thyroid Cancer: C Cell Story Revisited.. Eur Thyroid J 2016 Jul;5(2):79-93.
    doi: 10.1159/000447333pmc: PMC4949372pubmed: 27493881google scholar: lookup
  19. Fetter AW, Capen CC. Ultrastructural evaluation of thyroid parafollicular cells of pigs with naturally occurring atrophic rhinitis.. Pathol Vet 1970;7(2):170-85.
    doi: 10.1177/030098587000700211pubmed: 5535275google scholar: lookup
  20. Nunez EA, Krook L, Whalen JP. Effect of calcium depletion and subsequent repletion on parathyroids, parafollicular (C) cells and bone in the growing pig.. Cell Tissue Res 1976 May 13;168(3):373-84.
    doi: 10.1007/BF00215314pubmed: 1277274google scholar: lookup
  21. Igbokwe C.O., Ezeasor D.N.. Histological and immunohistochemical changes of the thyroid gland during the foetal and post-natal period of development in indigenous large white crossbred pigs. Bulg. J. Vet. Med. 2015;18:313–324.
    doi: 10.15547/bjvm.859google scholar: lookup
  22. Blähser S. Immunocytochemical demonstration of calcitonin-containing C-cells in the thyroid glands of different mammals.. Cell Tissue Res 1978 Jan 31;186(3):551-8.
    doi: 10.1007/BF00224943pubmed: 342107google scholar: lookup
  23. Tanimura N, Tateyama S, Nosaka D, Moritomo Y, Yamaguchi R. Immunohistochemical and electron microscopical detection of parafollicular (C) cells in equine parathyroid glands.. Nihon Juigaku Zasshi 1986 Feb;48(1):45-52.
    doi: 10.1292/jvms1939.48.45pubmed: 3515007google scholar: lookup
  24. De Cock HE, MacLachlan NJ. Simultaneous occurrence of multiple neoplasms and hyperplasias in the adrenal and thyroid gland of the horse resembling multiple endocrine neoplasia syndrome: case report and retrospective identification of additional cases.. Vet Pathol 1999 Nov;36(6):633-6.
    doi: 10.1354/vp.36-6-633pubmed: 10568452google scholar: lookup
  25. Kuwamura M, Shirota A, Yamate J, Kotani T, Ohashi F, Sakuma S. C-cell adenoma containing variously sized thyroid follicles in a horse.. J Vet Med Sci 1998 Mar;60(3):387-9.
    doi: 10.1292/jvms.60.387pubmed: 9560793google scholar: lookup
  26. Piñeyro P, Vieson MD, Ramos-Vara JA, Moon-Larson M, Saunders G. Histopathological and immunohistochemical findings of primary and metastatic medullary thyroid carcinoma in a young dog.. J Vet Sci 2014;15(3):449-53.
    doi: 10.4142/jvs.2014.15.3.449pmc: PMC4178149pubmed: 24690600google scholar: lookup
  27. Seimiya YM, Takahashi M, Furukawa T, Mizutani K, Kimura K, Haritani M. An aged bull with concurrent thyroid C cell carcinoma, adrenal pheochromocytoma and pituitary chromophobe adenoma.. J Vet Med Sci 2009 Feb;71(2):225-8.
    doi: 10.1292/jvms.71.225pubmed: 19262038google scholar: lookup
  28. Yoshikawa T, Yoshikawa H, Oyamada T, Suzuki K. A follicular adenoma with C-cell hyperplasia in the equine thyroid.. Nihon Juigaku Zasshi 1984 Oct;46(5):615-23.
    doi: 10.1292/jvms1939.46.615pubmed: 6513233google scholar: lookup
  29. Martín-Lacave I, Conde E, Montero C, Galera-Davidson H. Quantitative changes in the frequency and distribution of the C-cell population in the rat thyroid gland with age.. Cell Tissue Res 1992 Oct;270(1):73-7.
    doi: 10.1007/BF00381881pubmed: 1423525google scholar: lookup
  30. McMillan PJ, Hooker WM, Deptos LJ. Distribution of calcitonin-containing cells in the human thyroid.. Am J Anat 1974 May;140(1):73-9.
    doi: 10.1002/aja.1001400106pubmed: 4824765google scholar: lookup
  31. Bagiński S.. Technika Mikroskopowa; Praktyczny Poradnik Mikroskopowy. PWN; Warsaw, Poland: 1965. p. 367.
  32. Cameselle-Teijeiro J, Varela-Durán J, Sambade C, Villanueva JP, Varela-Núñez R, Sobrinho-Simoes M. Solid cell nests of the thyroid: light microscopy and immunohistochemical profile.. Hum Pathol 1994 Jul;25(7):684-93.
    doi: 10.1016/0046-8177(94)90302-6pubmed: 7517912google scholar: lookup
  33. Mizukami Y, Nonomura A, Michigishi T, Noguchi M, Hashimoto T, Nakamura S, Ishizaki T. Solid cell nests of the thyroid. A histologic and immunohistochemical study.. Am J Clin Pathol 1994 Feb;101(2):186-91.
    doi: 10.1093/ajcp/101.2.186pubmed: 7509563google scholar: lookup
  34. Collins WT, Capen CC, Döbereiner J, Tokarnia CH. Ultrastructural evaluation of parathyroid glands and thyroid C cells of cattle fed Solanum malacoxylon.. Am J Pathol 1977 Jun;87(3):603-14.
    doi: 10.1017/S0424820100090816pmc: PMC2032141pubmed: 869016google scholar: lookup
  35. Ljungberg O, Nilsson PO. Hyperplastic and neoplastic changes in ultimobranchial remnants and in parafollicular (C) cells in bulls: a histologic and immunohistochemical study.. Vet Pathol 1985 Mar;22(2):95-103.
    doi: 10.1177/030098588502200201pubmed: 2858934google scholar: lookup
  36. Sawicki B.. Ultimobranchial follicles and cysts in the European bison thyroid. Acta Theriol 1991;36:349–356.
    doi: 10.4098/AT.arch.91-35google scholar: lookup
  37. Sawicki B., Siuda S., Kasacka I.. Microscopic structure of the thyroid gland in the European bison. Acta Theriol 1992;37:171–179.
    doi: 10.4098/AT.arch.92-17google scholar: lookup
  38. Hazard JB. The C cells (parafollicular cells) of the thyroid gland and medullary thyroid carcinoma. A review.. Am J Pathol 1977 Jul;88(1):213-50.
    pmc: PMC2032150pubmed: 18012
  39. Das SS, Mishra S, Kaul JM. Development of Parafollicular Cells and their Relationship with Developing Thyroid Follicles in Human Foetuses.. J Clin Diagn Res 2017 Jul;11(7):AC01-AC04.
  40. Lin YT. [Immunoperoxidase staining studies on C-cells in fresh human thyroid].. Nihon Naibunpi Gakkai Zasshi 1983 Sep 20;59(9):1244-55.
  41. Wolfe HJ, DeLellis RA, Voelkel EF, Tashjian AH Jr. Distribution of calcitonin-containing cells in the normal neonatal human thyroid gland: a correlation of morphology with peptide content.. J Clin Endocrinol Metab 1975 Dec;41(06):1076-81.
    doi: 10.1210/jcem-41-6-1076pubmed: 1206094google scholar: lookup
  42. Kameda Y. Parafollicular cells of the thyroid as studied with Davenport's silver impregnation.. Arch Histol Jpn 1968 Dec;30(1):83-94.
    doi: 10.1679/aohc1950.30.83pubmed: 4181225google scholar: lookup

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