In situ localization of lectin-binding glycoconjugates in the matrix of growth-plate cartilage.

C E Farnum, N J Wilsman
{"title":"In situ localization of lectin-binding glycoconjugates in the matrix of growth-plate cartilage.","authors":"C E Farnum,&nbsp;N J Wilsman","doi":"10.1002/aja.1001760106","DOIUrl":null,"url":null,"abstract":"<p><p>In the distal hypertrophic zone of growth-plate cartilage, the pericellular matrix surrounding individual chondrocytes and the territorial matrix uniting chondrocytes into columnar groups are invaded by metaphyseal endothelial cells prior to osteogenesis. In the present study, lectin-binding glycoconjugates were analyzed in these two matrix compartments of growth-plate cartilage from Yucatan swine. Nine lectin-fluorescein conjugates were tested by a postembedment method on 1-micron-thick, nondecalcified, Epon-embedded sections. Chondrocytes in all cellular zones were surrounded by a pericellular matrix which showed positive binding for peanut agglutinin (PNA), ricin agglutinin (RCA-I), and soybean agglutinin (SBA). Binding by these lectins was sensitive to digestion with hyaluronidase, chondroitinase, and trypsin. Pericellular glyconconjugtes that bind RCA-I and concanvalin A (CONA) after periodic acid oxidation, and which were sensitive to trypsin but not to chondroitinase or hyaluronidase, were present in the hypertrophic cell zone. Within the territorial matrix, binding of lectins specific for galactose, N-acetylgalactosamine, and fucose showed gradients of intensity which became maximal at the last transverse septum. Lectin-binding histochemistry more precisely differentiated the microheterogeneity of glycoconjugate distribution within these two matrix compartments than has been possible with other histochemical techniques. Lectin-binding affinity is a potentially useful technique by which to isolate cartilage matrix macromolecules unique to specific cellular zones of the growth plate.</p>","PeriodicalId":50815,"journal":{"name":"American Journal of Anatomy","volume":"176 1","pages":"65-82"},"PeriodicalIF":0.0000,"publicationDate":"1986-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/aja.1001760106","citationCount":"19","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Anatomy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/aja.1001760106","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 19

Abstract

In the distal hypertrophic zone of growth-plate cartilage, the pericellular matrix surrounding individual chondrocytes and the territorial matrix uniting chondrocytes into columnar groups are invaded by metaphyseal endothelial cells prior to osteogenesis. In the present study, lectin-binding glycoconjugates were analyzed in these two matrix compartments of growth-plate cartilage from Yucatan swine. Nine lectin-fluorescein conjugates were tested by a postembedment method on 1-micron-thick, nondecalcified, Epon-embedded sections. Chondrocytes in all cellular zones were surrounded by a pericellular matrix which showed positive binding for peanut agglutinin (PNA), ricin agglutinin (RCA-I), and soybean agglutinin (SBA). Binding by these lectins was sensitive to digestion with hyaluronidase, chondroitinase, and trypsin. Pericellular glyconconjugtes that bind RCA-I and concanvalin A (CONA) after periodic acid oxidation, and which were sensitive to trypsin but not to chondroitinase or hyaluronidase, were present in the hypertrophic cell zone. Within the territorial matrix, binding of lectins specific for galactose, N-acetylgalactosamine, and fucose showed gradients of intensity which became maximal at the last transverse septum. Lectin-binding histochemistry more precisely differentiated the microheterogeneity of glycoconjugate distribution within these two matrix compartments than has been possible with other histochemical techniques. Lectin-binding affinity is a potentially useful technique by which to isolate cartilage matrix macromolecules unique to specific cellular zones of the growth plate.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
生长板软骨基质中凝集素结合糖的原位定位。
在生长板软骨的远端肥大带,单个软骨细胞周围的细胞周基质和将软骨细胞联合成柱状群的区域基质在成骨之前被干骺端内皮细胞侵袭。本研究在尤卡坦猪生长板软骨的这两个基质室中分析了凝集素结合糖缀合物。9种凝集素-荧光素偶联物在1微米厚、非脱钙、epon包埋切片上采用包埋后方法进行检测。所有细胞带的软骨细胞都被细胞周基质包围,其与花生凝集素(PNA)、蓖麻毒素凝集素(rca - 1)和大豆凝集素(SBA)结合呈阳性。这些凝集素的结合对透明质酸酶、软骨素酶和胰蛋白酶的消化很敏感。细胞周围糖偶联物在周期性酸氧化后结合rca - 1和CONA (CONA),对胰蛋白酶敏感,但对软骨素酶或透明质酸酶不敏感,存在于肥大细胞区。在区域基质内,半乳糖特异性凝集素、n -乙酰半乳糖胺特异性凝集素与病灶的结合呈现强度梯度,并在最后横隔处达到最大。与其他组织化学技术相比,凝集素结合组织化学更精确地区分了这两个基质室中糖缀合物分布的微观异质性。凝集素结合亲和是一种潜在的有用的技术,通过它分离软骨基质大分子独特的特定细胞区域的生长板。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The Role of Foveal Cortex in Discriminating Peripheral Stimuli: The Sketchpad Hypothesis. Association of Lymphovascular Space Invasion With Locoregional Failure and Survival in Patients With Node-Negative Oral Tongue Cancers. Early Minocycline and Late FK506 Treatment Improves Survival and Alleviates Neuroinflammation, Neurodegeneration, and Behavioral Deficits in Prion-Infected Hamsters. Trimethylamine N-Oxide and Mortality Risk in Patients With Peripheral Artery Disease. Proliferation in the genital tract of the normal mature guinea pig treated with colchicine
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1