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   <subfield code="a">Immunoelectron microscopic studies of glycosaminoglycans in the metaphyseal bone trabeculae of growing rats</subfield>
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   <subfield code="c">[Toshitada Kazama, Minoru Takagi, Teruhiko Ishii, Yoshihisa Toda]</subfield>
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   <subfield code="a">Summary: The types and distribution of glycosaminoglycans (GAGs) were studied immunocytochemically in osteoid, mineralized bone matrix, and cartilage matrix of growing rat metaphyseal bone after aldehyde fixation and EDTA demineralization, using four monoclonal antibodies (mAbs 1-B-5, 2-B-6, 3-B-3 and 5-D-4). These mAbs specifically recognize epitopes in non-sulphated chondroitin (C0-S); chondroitin 4-sulphate (C4-S) and dermatan sulphate (DS); chondroitin 6-sulphate (C6-S) and C0-S; and keratan sulphate (KS) respectively. In osteoid, all mAbs except 1-B-5 weakly stained matrix material on and between collagen fibrils, and moderately stained organic material corresponding to bone nodules, which are known sites of mineralization. However, the staining of osteoid abruptly decreased at the mineralization front; weak staining was confined mostly to the organic material of bone nodules in mineralized bone matrix, with very weak or no staining of the rest of the bone matrix. This staining progressively decreased toward the mineralized cartilage matrix and became negative. The mineralized cartilage matrix and lamina limitans reacted strongly with all mAbs except 5-D-4. These results indicate that osteoid contains sulphated proteoglycans containing C4-S and/or DS, C6-S and KS, and subsequent bone matrix mineralization appears to require accumulation of these macromolecules within bone nodules and eventual loss of these substances for complete mineralization, whereas proteoglycans containing C0-S, C4-S and/or DS, and C6-S, still exist in mineralized cartilage matrix and lamina limitants.</subfield>
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   <subfield code="a">Kazama</subfield>
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   <subfield code="u">Department of Oral Surgery (TK, TI) and Anatomy (MT, YT), Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, 101, Chiyoda-ku, Tokyo, Japan</subfield>
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   <subfield code="a">Takagi</subfield>
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   <subfield code="u">Department of Oral Surgery (TK, TI) and Anatomy (MT, YT), Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, 101, Chiyoda-ku, Tokyo, Japan</subfield>
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   <subfield code="u">Department of Oral Surgery (TK, TI) and Anatomy (MT, YT), Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, 101, Chiyoda-ku, Tokyo, Japan</subfield>
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   <subfield code="u">Department of Oral Surgery (TK, TI) and Anatomy (MT, YT), Nihon University School of Dentistry, 1-8-13 Kanda-Surugadai, 101, Chiyoda-ku, Tokyo, Japan</subfield>
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   <subfield code="t">The Histochemical Journal</subfield>
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   <subfield code="g">24/10(1992-10-01), 747-755</subfield>
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