scholarly journals Variations in the Total Number of Epithelial Cells Isolated from the Mucosa of Small Intestine in Mice under Various Experimental Conditions

1969 ◽  
Vol 81 (5-6) ◽  
pp. 429-434
Author(s):  
Ryoich INABA
Parasitology ◽  
1976 ◽  
Vol 73 (3) ◽  
pp. 371-380 ◽  
Author(s):  
J. P. Dubey ◽  
R. Fayer

The life-cycle of canine Isospora bigemina was studied in dogs, cattle, cats and mice. Under experimental conditions dogs served as both definitive and intermediate hosts. Unsporulated oocysts (11 × 12 μm) were shed in the faeces and sporulated outside the host within 12 h at 30–37 °C and 36 to 48 h at 23 °C. Sporulated oocysts measured 12 × 13 μm and contained 2 sporocysts which in turn contained 4 sporozoites. Sporocysts averaged 6 × 9 μm and sporozoites averaged 2 × 6 μm. Although no stages were found microscopically in tissues or in faeces of 23 dogs orally inoculated with sporulated oocysts, the oocysts were infectious because 5 of 14 dogs that ingested tissues of dogs fed oocysts, shed oocysts. Prepatent periods were 7 to 15 days; patency was 1–3 days. No dogs became ill. In the naturally infected dog and one experimentally infected dog, schizonts were found in epithelial cells, distal to the host cell nucleus at the tips of villi throughout the small intestine. Schizonts were 5–7 μm and contained 3–12 merozoites. In the naturally infected dog, gametes were found in the same location. Male gametocytes were 6–8 μm and contained 6–12 microgametes, and female gametes were 7–8 μm.Sporulated I. bigemina oocysts from a naturally infected dog were not infectious to cattle, cats or mice. Structurally identical oocysts were shed by 2 dogs after ingesting hearts and diaphragm from naturally infected cattle; these oocysts were also not infectious to cattle. Although dogs acted as both intermediate and definitive hosts under experimentation, this is not likely to occur in nature. A canine-bovine-canine cycle would appear to be the natural mode of infection but I. bigemina was not infectious to cattle under experimental conditions.


Author(s):  
A. J. Tousimis

The elemental composition of amino acids is similar to that of the major structural components of the epithelial cells of the small intestine and other tissues. Therefore, their subcellular localization and concentration measurements are not possible by x-ray microanalysis. Radioactive isotope labeling: I131-tyrosine, Se75-methionine and S35-methionine have been successfully employed in numerous absorption and transport studies. The latter two have been utilized both in vitro and vivo, with similar results in the hamster and human small intestine. Non-radioactive Selenomethionine, since its absorption/transport behavior is assumed to be the same as that of Se75- methionine and S75-methionine could serve as a compound tracer for this amino acid.


Author(s):  
D.S. Friend ◽  
N. Ghildyal ◽  
M.F. Gurish ◽  
K.F. Austen ◽  
R.L. Stevens

Trichinella spiralis induces a profound mastocytosis and eosinophilia in the small intestine of the infected mouse. Mouse mast cells (MC) store in their granules various combinations of at least five chymotryptic chymases [designated mouse MC protease (mMCP) 1 to 5], two tryptic proteases designated mMCP-6 and mMCP-7 and an exopeptidase, carboxypeptidase A (mMC-CPA). Using antipeptide, protease -specific antibodies to these MC granule proteases, immunohistochemistry was done to determine the distribution, number and protease phenotype of the MCs in the small intestine and spleen 10 to >60 days after Trichinella infection of BALB/c and C3H mice. TEM was performed to evaluate the granule morphology of the MCs between intestinal epithelial cells and in the lamina propria (mucosal MCs) and in the submucosa, muscle and serosa of the intestine (submucosal MCs).As noted in the table below, the number of submucosal MCs remained constant throughout the study. In contrast, on day 14, the number of MCs in the mucosa increased ~25 fold. Increased numbers of MCs were observed between epithelial cells in the mucosal crypts, in the lamina propria and to a lesser extent, between epithelial cells of the intestinal villi.


2006 ◽  
Vol 50 (2) ◽  
pp. 198-200
Author(s):  
Juliana Fariña ◽  
M. Concepción Millana ◽  
M<sup>a</sup> Jesús Fernández-Aceñero ◽  
Vanessa Campo-Ruiz

1989 ◽  
Vol 109 (3) ◽  
pp. 1057-1069 ◽  
Author(s):  
A Marxer ◽  
B Stieger ◽  
A Quaroni ◽  
M Kashgarian ◽  
H P Hauri

The previously produced monoclonal antibody IEC 1/48 against cultured rat intestinal crypt cells (Quaroni, A., and K. J. Isselbacher. 1981. J. Natl. Cancer Inst. 67:1353-1362) was extensively characterized and found to be directed against the beta subunit of (Na+ + K+)-ATPase as assessed by immunological and enzymatic criteria. Under nondenaturing conditions the antibody precipitated the alpha-beta enzyme complex (98,000 and 48,000 Mr). This probe, together with the monoclonal antibody C 62.4 against the alpha subunit (Kashgarian, M., D. Biemesderfer, M. Caplan, and B. Forbush. 1985. Kidney Int. 28:899-913), was used to localize (Na+ + K+)-ATPase in epithelial cells along the rat intestinal tract by immunofluorescence and immunoelectron microscopy. Both antibodies exclusively labeled the basolateral membrane of small intestine and proximal colon epithelial cells. However, in the distal colon, IEC 1/48, but not C 62.4, also labeled the brush border membrane. The cross-reacting beta-subunit-like antigen on the apical cell pole was tightly associated with isolated brush borders but was apparently devoid of (Na+ + K+)-ATPase activity. Subcellular fractionation of colonocytes in conjunction with limited proteolysis and surface radioiodination of intestinal segments suggested that the cross-reacting antigen in the brush border may be very similar to the beta subunit. The results support the notion that in the small intestine and proximal colon the enzyme subunits are exclusively targeted to the basolateral membrane while in the distal colon nonassembled beta subunit or a beta-subunit-like protein is also transported to the apical cell pole.


1971 ◽  
Vol 8 (5-6) ◽  
pp. 490-505 ◽  
Author(s):  
C. A. Mebus ◽  
E. L. Stair ◽  
N. R. Underdahl ◽  
M. J. Twiehaus

Gross, immunofluorescent, and light microscopic findings in seven gnotobiotic calves inoculated orally with a Reo-like neonatal calf diarrhea virus were compared to findings in three control gnotobiotic calves. Neonatal calf diarrhea virus infected primarily the villous epithelium of the small intestine. Calves examined within 1.5 h after onset of diarrhea had tall columnar immunofluorescent villous epithelial cells in the middle and lower small intestine. Calves examined 2–4.5 h after onset of diarrhea had cuboidal to squamous villous epithelial cells and an increase in reticulum-like cells in the villous lamina propria of the middle and lower small intestine. Viral tilers were 106 and 108 in colonic contents from two calves inoculated with cell-culture-adapted virus and necropsied, respectively, 2 and 6 h after onset of diarrhea.


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