Histogenetic Stereological Reconstruction of Rat Basophilic, Clear, and Oncocytic Neoplastic Renal Cell Lesions Using Carbonic Anhydrase Type II-PAS Double-Stained Sections

Author:

Tsuda Hiroyuki1,Iwase Teruhiko2,Matsumoto Kazuyuki2,Ito Mitsuya2,Hirono Iwao2,Nishida Yoshihisa3,Takasuka Nobuo4,Iwahori Yoshio4,Ota Tomonori4,Dae Joong Kim 4,Kadenbach Bernhard5

Affiliation:

1. Experimental Pathology and Chemotherapy Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104, Japan,

2. Second Department of Pathology, Fujita Health University School of Medicine, Kutsukake-cho, Toyoake, Aichi, Japan

3. Department of Pediatric Surgery, Fujita Health University School of Medicine, Kutsukake-cho, Toyoake, Aichi, Japan

4. Experimental Pathology and Chemotherapy Division, National Cancer Center Research Institute, 5-1-1 Tsukiji, Chuo-ku, Tokyo 104, Japan

5. Fachbereich Chemie der Philips-Universitšt, Hans-Meerwein-Stra§e, Lahnberge, D-3550 Marburg, Germany

Abstract

The histogenesis of 3 types of rat renal cell tumors (basophilic cell, clear cell, and oncocytic) was stereologically analyzed, with particular attention paid to transitions from normal tubules. Early nitrosamine-induced preneoplastic lesions, including dysplastic tubules (altered tubules), epithelial hyperplasias, and small adenomas, were reconstructed using serially sectioned specimens processed for carbonic anhydrase type II (CA) and periodic acid-Schiff (PAS) (CA-PAS) double staining to allow easier distinction of the nephron segments: Proximal tubules had a PAS-positive brush border and were weakly positive for CA in the cytoplasm; distal tubules were PAS negative and weakly positive for CA; collecting ducts were PAS negative and strongly positive for CA. Similarly, cytochrome c oxidase (CytOx) and CytOx-PAS double staining was also applied to confirm the character of oncocytic lesions. All basophilic lesions (7 of 7) showed transition to proximal tubules. Clear cell lesions positive for CA, on the other hand, showed transition to distal tubules in 4 of 9 (44.4%) lesions and to collecting ducts in 4 of 9 (44.4%) lesions, but in only 1 of 9 (11%) to a proximal tubule. All oncocytic lesions (16 of 16), characterized by positivity for both CA and CytOx, showed transition to collecting ducts. The results indicate that the origins of renal cell neoplasia are proximal tubules for the basophilic cell lesions, either proximal or distal tubules for their clear cell counterparts, and collecting ducts for oncocytic lesions.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

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