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Localization of worm antigen in Neodiplostomum seoulense by immuno-electronmicroscopy
J C Lee,1Y Kong,2S U Lee,3 and S Huh*3
1Research and Development Center, Samchundang Pharmatheutical Company, Chunchon 200-060, Korea.
Received February 06, 1997; Accepted March 07, 1997.
Abstract
The localization of worm antigen of Neodiplostomum seoulense was examined by immuno-electronmicroscopic observation. Not only the immunized serum of mice with crude worm extract of N. seoulense but also serum of infected mouse were reacted to the worm section. Using immunized serum as primary antibody, the gold particles were deposited on the rough endoplasmic reticulum of the cell of tribocytic organ, spermatozoa in the seminal vesicle, microvilli of the caecum and vitelline follicle. Using infected serum, gold particles were deposited only on the vitelline follicle prominently. This finding suggested that the tribocytic organ, seminal vesicle, caeca and vitelline follicles may play a role of antigen to immunized serum with crude worm extract of N. seoulense, whereas the vitelline follicle, to the infected serum.
Figures
Figs. 1-2 Fig. 1. Tegument of Neodiplostomum seoulense treated with immunized serum. A few number of gold particles were deposited on the rough endoplasmic reticulum (rER). S: spine, CM: circular muscle, LM: longitudinal muscle, G: granule, M: mitochodria, N: nucleus. Fig. 2. Tegument of N. seoulense treated with infected serum. A very few number of gold particles were deposited on the rER. M: mitochondria, N: nucleus.
Figs. 3-5 Fig. 3. Tribocytic organ of N. seoulense treated with immunized serum. Gold particles (13 ± 2 particles/0.1 µm2) were deposited on the rough endoplasmic reticulum (ER). G: granule. Fig. 4. Ibid. High magnification. Fig. 5. Tribocytic organ of N. seoulense treated with infected serum. Gold particles (2 ± 1 particles/0.1 µm2) were deposited on the rER. G: granule.
Figs. 6-8 Fig. 6. Spermatozoa in the seminal vesicle treated with immunized serum. Gold particles were deposited on the interstitial matrix between spermatozoa. Fig. 7. Spermatozoa in the seminal vesicle treated with infected serum. Gold particles were deposited on the interstitial matrix between spermatozoa. Fig. 8. Head of spermatozoa in the seminal vesicle treated with immunized serum. Gold particles (31 ± 4 particles/0.1 µm2) were deposited on the space surrounding sperm head.
Figs. 9-10 Fig. 9. Microvilli of the caeca treated with immunized serum. Gold particles (28 ± 2 particles/0.1 µm2) were deposited on the microvilli (V) of caeca. Fig. 10. Microvilli of the caeca treated with infected serum. Gold particles (4 ± 2 particles/0.1 µm2) were deposited on the microvilli (V) of caeca.
Figs. 11-12 Fig. 11. Vitelline follicle treated with immunized serum. Gold particles (34 ± 4 particles/0.1 µm2) were deposited on the interstitial area between and surrounding the granules of the vitelline follicle (F). Fig. 12. Vitelline follicle treated with infected serum. Gold particles (16 ± 3 particles/0.1 µm2) were deposited on the interstitial area between and surrounding the granules of the vitelline follicle (F).
Tables
Table 1 Quantitative analysis of immunogold particles in the section of Neodiplostomum seoulense with immunized serum and with infected serum
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