Analyze Diet
Cells, tissues, organs2002; 172(1); 29-36; doi: 10.1159/000064389

Immunohistochemical localization of chromogranin a in the acinar cells of equine salivary glands contrasts with rodent glands.

Abstract: We investigated the existence of chromogranin A (CgA) in salivary glands of the horse by Western blotting and enzyme immunoassay (EIA) using an antiserum against a peptide sequence of equine CgA. We also compared its cellular distribution between the horse and rat salivary glands with a tyramide signal amplification immunofluorescence technique. Western blotting gave three significant immunoreactive bands (74, 56 and 48 kDa) in adrenal medulla and three major salivary glands of horses. Immunoreactivities for CgA measured by EIA in horses were 154.05 +/- 41.46, 20.32 +/- 5.59 and 4.43 +/- 2.23 pmol/g wet weight in the parotid gland, submandibular gland and sublingual gland, respectively, and 1.03 +/- 0.407 pmol/mg protein in the saliva. Immunohistochemically, the positive reactivity was mainly recognized at acinar cells in equine salivary glands. This exhibits a contrast to the finding in the rat salivary glands that the CgA immunoreactivity is localized at the duct cells of the submandibular gland. These results provide novel evidence that in the horse, CgA is stored in the acinar cells of salivary glands, and secreted into saliva.
Publication Date: 2002-10-05 PubMed ID: 12364826DOI: 10.1159/000064389Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Comparative Study
  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research looks into the presence of a protein called chromogranin A (CgA) in horse salivary glands. Its storage and secretion from the salivary glands are in the acinar cells, unlike in rats where it’s found in the ductal cells.

Methods

  • The researchers used Western blotting and enzyme immunoassay (EIA) to determine if CgA was present in horses’ salivary glands. These techniques used an antiserum against a peptide sequence specific to equine CgA.
  • They compared the distribution of CgA in horse and rat salivary glands through an immunofluorescence technique known as tyramide signal amplification (TSA).

Results

  • The testing revealed three significant immunoreactive bands in both the adrenal medulla – the inner part of the adrenal gland – and the three major salivary glands (parotid, submandibular, and sublingual) of horses. These bands, with weights of 74, 56, and 48 kDa, indicate the presence of CgA.
  • More specifically, they measured the immunoreactivity of CgA in horse by EIA. The values were highest in the parotid gland, followed by the submandibular and sublingual glands, and was lowest in the saliva.
  • Immunohistochemical detection showed positive CgA reactivity mainly in the acinar cells of horse salivary glands. This contrasts the findings in rats where CgA is mostly localized in the duct cells of the submandibular gland.

Conclusion

  • The findings provide evidence indicating that in horses, CgA is stored in the acinar cells of the salivary glands, different from its storage location in rats. From here, it is secreted into the saliva.

Significance

  • The differences in localization of CgA between species highlight the importance of comprehensive interspecies studies before applying findings to other species. This is of particular relevance in areas such as drug development where animal models often serve as the first step.

Cite This Article

APA
Sato F, Kanno T, Nagasawa S, Yanaihara N, Ishida N, Hasegawa T, Iwanaga T. (2002). Immunohistochemical localization of chromogranin a in the acinar cells of equine salivary glands contrasts with rodent glands. Cells Tissues Organs, 172(1), 29-36. https://doi.org/10.1159/000064389

Publication

ISSN: 1422-6405
NlmUniqueID: 100883360
Country: Switzerland
Language: English
Volume: 172
Issue: 1
Pages: 29-36

Researcher Affiliations

Sato, Fumio
  • Laboratory of Molecular and Cellular Biology, Equine Research Institute, Japan Racing Association, Utsunomiya, Japan. fumios@center.equinst.go.jp
Kanno, Tomio
    Nagasawa, Shingo
      Yanaihara, Noboru
        Ishida, Nobushige
          Hasegawa, Telhisa
            Iwanaga, Toshihiko

              MeSH Terms

              • Animals
              • Chromogranin A
              • Chromogranins / metabolism
              • Epithelial Cells / metabolism
              • Epithelial Cells / ultrastructure
              • Female
              • Horses / anatomy & histology
              • Horses / metabolism
              • Immunohistochemistry
              • Male
              • Microscopy, Electron
              • Rats
              • Rats, Wistar / anatomy & histology
              • Rats, Wistar / metabolism
              • Salivary Glands / metabolism
              • Salivary Glands / ultrastructure
              • Secretory Vesicles / metabolism
              • Secretory Vesicles / ultrastructure
              • Stress, Physiological / diagnosis
              • Stress, Physiological / metabolism
              • Sympathetic Fibers, Postganglionic / metabolism

              Citations

              This article has been cited 8 times.
              1. Kaiser M, Jacobsen S, Andersen PH, Bækbo P, Cerón JJ, Dahl J, Escribano D, Theil PK, Jacobson M. Hormonal and metabolic indicators before and after farrowing in sows affected with postpartum dysgalactia syndrome.. BMC Vet Res 2018 Nov 7;14(1):334.
                doi: 10.1186/s12917-018-1649-zpubmed: 30404636google scholar: lookup
              2. Srithunyarat T, Hagman R, Höglund OV, Olsson U, Stridsberg M, Jitpean S, Lagerstedt AS, Pettersson A. Catestatin and vasostatin concentrations in healthy dogs.. Acta Vet Scand 2017 Jan 3;59(1):1.
                doi: 10.1186/s13028-016-0274-8pubmed: 28049540google scholar: lookup
              3. Martínez-Miró S, Tecles F, Ramón M, Escribano D, Hernández F, Madrid J, Orengo J, Martínez-Subiela S, Manteca X, Cerón JJ. Causes, consequences and biomarkers of stress in swine: an update.. BMC Vet Res 2016 Aug 19;12(1):171.
                doi: 10.1186/s12917-016-0791-8pubmed: 27543093google scholar: lookup
              4. Soell M, Feki A, Hannig M, Sano H, Pinget M, Selimovic D. Chromogranin A detection in saliva of type 2 diabetes patients.. Bosn J Basic Med Sci 2010 Feb;10(1):2-8.
                doi: 10.17305/bjbms.2010.2725pubmed: 20192923google scholar: lookup
              5. Kanai K, Hino M, Hori Y, Nakao R, Hoshi F, Itoh N, Higuchi S. Circadian variations in salivary chromogranin a concentrations during a 24-hour period in dogs.. J Vet Sci 2008 Dec;9(4):421-3.
                doi: 10.4142/jvs.2008.9.4.421pubmed: 19052500google scholar: lookup
              6. Hamaguchi T, Fukudo S, Kanazawa M, Tomiie T, Shimizu K, Oyama M, Sakurai K. Changes in salivary physiological stress markers induced by muscle stretching in patients with irritable bowel syndrome.. Biopsychosoc Med 2008 Nov 4;2:20.
                doi: 10.1186/1751-0759-2-20pubmed: 18983682google scholar: lookup
              7. Gorr SU, Venkatesh SG, Darling DS. Parotid secretory granules: crossroads of secretory pathways and protein storage.. J Dent Res 2005 Jun;84(6):500-9.
                doi: 10.1177/154405910508400604pubmed: 15914585google scholar: lookup
              8. Feldman SA, Eiden LE. The chromogranins: their roles in secretion from neuroendocrine cells and as markers for neuroendocrine neoplasia.. Endocr Pathol 2003 Spring;14(1):3-23.
                doi: 10.1385/ep:14:1:3pubmed: 12746559google scholar: lookup