Localization of cytoskeletal proteins in Pneumocystis carinii by immuno-electron microscopy.
10.3347/kjp.2001.39.1.13
- Author:
Jae Ran YU
;
Jae Kyong PYON
;
Min SEO
;
Byung Suk JUNG
;
Sang Rock CHO
;
Soon Hyung LEE
;
Sung Tae HONG
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- MeSH:
Actins/analysis;
Animals;
Cytoskeletal Proteins/*analysis;
Fungal Proteins/*analysis;
Histocytochemistry;
Microscopy, Immunoelectron;
Pneumocystis/*chemistry/cytology;
Rats;
Rats, Wistar;
Support, Non-U.S. Gov't;
Tropomyosin/analysis;
Tubulin/analysis
- From:The Korean Journal of Parasitology
2001;39(1):13-21
- CountryRepublic of Korea
- Language:English
-
Abstract:
Pneumocystis carinii causes serious pulmonary infection in immunosuppressed patients. This study was undertaken to observe the cytoskeletal proteins of P. carinii by immuno-electron microscopy. P. carinii infection was experimentally induced by immunosuppression of Sprague-Dawley rats for seven weeks, and their lungs were used for the observations of this study. The gold particles localized actin, tropomyosin, and tubulin. The actin was irregularly scattered in the cytoplasm of the trophic forms but was much more concentrated in the inner space of the cell wall of the cystic forms called the inner electron-lucent layer. No significant amount of tropomyosin was observed in either trophic forms or cystic forms. The tubulin was distributed along the peripheral cytoplasm and filopodia of both the trophic and cystic forms rather than in the inner side of the cytoplasm. Particularly, in the cystic forms, the amount of tubulin was increased and located mainly in the inner electron-lucent layer of the cell wall where the actin was concentrated as well. The results of this study showed that the cell wall of P. carinii cystic forms is a structure whose inner side is rich in actin and tubulin. The location of the actin and tubulin in P. carinii suggests that the main role of these proteins is an involvement in the protection of cystic forms from the outside environment by maintaining rigidity of the cystic forms.
