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Journal of Anatomy logoLink to Journal of Anatomy
. 1996 Dec;189(Pt 3):623–630.

Distribution of alpha-vascular smooth muscle actin in the smooth muscle cells of the gastrointestinal tract of the chicken.

Y Yamamoto 1, T Kubota 1, Y Atoji 1, Y Suzuki 1
PMCID: PMC1167705  PMID: 8982838

Abstract

Immunoreactivity specific for alpha-vascular smooth muscle actin (ASMA) was examined in the enteric smooth muscle cells along the entire length of the gastrointestinal tract of the chicken. Specificity for gamma-smooth muscle actin (GSMA) and desmin was also examined. All smooth muscle layers, i.e. the muscularis mucosae, and the circular and longitudinal muscle layers, showed immunoreactivity specific for GSMA and desmin throughout the gastrointestinal tract whereas immunoreactivity for ASMA differed between regions and muscle layers. In the oesophagus and crop, immunoreactivity for ASMA was observed in the muscularis mucosae and the inner and outer muscle layers, together with staining for GSMA and desmin. In the proventriculus, immunoreactivity for ASMA was observed in all smooth muscle cells in the inner layer of the muscularis mucosae and the longitudinal muscle layer. In the outer layer of the muscularis mucosae, immunoreactivity for ASMA on smooth muscle cells was observed on the luminal side and decreased in the serosal direction. In the intermediate muscles, immunoreactivity for ASMA was observed in the luminal portion, the intensity of staining decreasing gradually in the serosal direction. In contrast to the intermediate muscles, the latter muscles were negative for ASMA. In the pyloric region, the outer part was weakly immunopositive, while the inner part was intensely positive. In the small and large intestines, the muscularis mucosae and the longitudinal muscle layer were positive for ASMA. The outer part of the circular muscle layer was immunonegative for ASMA whereas the inner part was positive. The complex structure and contractile functions of each organ and muscle layers may be related to the difference patterns of expression of ASMA molecules in the smooth muscle cells.

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Selected References

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  1. Bartlet A. L. Myogenic peristalsis in isolated preparations of chicken oesophagus. Br J Pharmacol. 1973 May;48(1):36–47. doi: 10.1111/j.1476-5381.1973.tb08220.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Chang K. S., Zimmer W. E., Jr, Bergsma D. J., Dodgson J. B., Schwartz R. J. Isolation and characterization of six different chicken actin genes. Mol Cell Biol. 1984 Nov;4(11):2498–2508. doi: 10.1128/mcb.4.11.2498. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Duke G. E. Gastrointestinal motility and its regulation. Poult Sci. 1982 Jul;61(7):1245–1256. doi: 10.3382/ps.0611245. [DOI] [PubMed] [Google Scholar]
  4. Faussone Pellegrini M. S., Cortesini C. Some ultrastructural features of the muscular coat of human small intestine. Acta Anat (Basel) 1983;115(1):47–68. doi: 10.1159/000145676. [DOI] [PubMed] [Google Scholar]
  5. Faussone-Pellegrini M. S., Pantalone D., Cortesini C. Morphological evidence for a cecocolonic junction in man and functional implications. Acta Anat (Basel) 1993;146(1):22–30. doi: 10.1159/000147416. [DOI] [PubMed] [Google Scholar]
  6. Gabbiani G., Schmid E., Winter S., Chaponnier C., de Ckhastonay C., Vandekerckhove J., Weber K., Franke W. W. Vascular smooth muscle cells differ from other smooth muscle cells: predominance of vimentin filaments and a specific alpha-type actin. Proc Natl Acad Sci U S A. 1981 Jan;78(1):298–302. doi: 10.1073/pnas.78.1.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Gabella G. Special muscle cells and their innervation in the mammalian small intestine. Cell Tissue Res. 1974;153(1):63–77. doi: 10.1007/BF00225446. [DOI] [PubMed] [Google Scholar]
  8. Gabella G. Structure of the musculature of the chicken small intestine. Anat Embryol (Berl) 1985;171(2):139–149. doi: 10.1007/BF00341408. [DOI] [PubMed] [Google Scholar]
  9. Hodgkiss J. P. Intrinsic reflexes underlying peristalsis in the small intestine of the domestic fowl. J Physiol. 1986 Nov;380:311–328. doi: 10.1113/jphysiol.1986.sp016287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Hodgkiss J. P. Peristalsis and antiperistalsis in the chicken caecum are myogenic. Q J Exp Physiol. 1984 Jan;69(1):161–170. doi: 10.1113/expphysiol.1984.sp002777. [DOI] [PubMed] [Google Scholar]
  11. Kobayashi S., Torihashi S., Iino S., Pang Y. W., Chowdhury J. U., Tomita T. The inner sublayer of the circular muscle coat in the canine proximal colon: origins of spontaneous electrical and mechanical activity. Arch Histol Cytol. 1995 Mar;58(1):45–63. doi: 10.1679/aohc.58.45. [DOI] [PubMed] [Google Scholar]
  12. Lessard J. L. Two monoclonal antibodies to actin: one muscle selective and one generally reactive. Cell Motil Cytoskeleton. 1988;10(3):349–362. doi: 10.1002/cm.970100302. [DOI] [PubMed] [Google Scholar]
  13. Rubenstein P. A. Differential behavior of gizzard isoactins. Arch Biochem Biophys. 1981 Sep;210(2):598–608. doi: 10.1016/0003-9861(81)90226-5. [DOI] [PubMed] [Google Scholar]
  14. Sawtell N. M., Hartman A. L., Lessard J. L. Unique isoactins in the brush border of rat intestinal epithelial cells. Cell Motil Cytoskeleton. 1988;11(4):318–325. doi: 10.1002/cm.970110409. [DOI] [PubMed] [Google Scholar]
  15. Skalli O., Ropraz P., Trzeciak A., Benzonana G., Gillessen D., Gabbiani G. A monoclonal antibody against alpha-smooth muscle actin: a new probe for smooth muscle differentiation. J Cell Biol. 1986 Dec;103(6 Pt 2):2787–2796. doi: 10.1083/jcb.103.6.2787. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Vandekerckhove J., Weber K. At least six different actins are expressed in a higher mammal: an analysis based on the amino acid sequence of the amino-terminal tryptic peptide. J Mol Biol. 1978 Dec 25;126(4):783–802. doi: 10.1016/0022-2836(78)90020-7. [DOI] [PubMed] [Google Scholar]
  17. Yamamoto Y., Atoji Y., Suzuki Y. Muscular architecture and VIP-like immunoreactive nerves in the gastroduodenal junction of the chicken. Vet Res Commun. 1995;19(2):85–93. doi: 10.1007/BF01839274. [DOI] [PubMed] [Google Scholar]
  18. Yamamoto Y., Kubota T., Atoji Y., Suzuki Y. Structure of the perilobular sheath of the deep proventricular gland of the chicken: presence and possible role of myofibroblasts. Cell Tissue Res. 1996 Jul;285(1):109–117. doi: 10.1007/s004410050626. [DOI] [PubMed] [Google Scholar]

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