Matrix metabolism and healing in the flexor tendon. Experimental studies on rabbit tendon.

S O Abrahamsson
{"title":"Matrix metabolism and healing in the flexor tendon. Experimental studies on rabbit tendon.","authors":"S O Abrahamsson","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>I. The rabbit flexor tendon within the synovial sheath contains segments with fibrocartilage-like areas. These segments have a higher proteoglycan and a lower collagen and non-collagen protein synthesis compared to the segment with \"true\" tendon tissue. Cell proliferation is also lower within the proximal segment than in the intermediate and distal segments. These regional variations should be considered when interpreting experimental data. They may also be of importance for the variable healing capacity of different flexor tendon regions. II. Recombinant human insulin-like growth factor, insulin and fetal calf serum stimulate matrix synthesis and cell proliferation in a dose dependent manner in flexor tendon explants cultured for three days. rhIGF-I was more potent than insulin in stimulating cell proliferation and matrix synthesis. rhIGF-I also stimulated matrix synthesis to a higher degree than FCS. III. In long-term culture of flexor tendon explants, the addition of rhIGF-I to the culture medium stimulates matrix synthesis, but does not influence turn-over rates. The total hexosamine and collagen contents in tendons cultured in medium with rhIGF-I remain at the same level, while non-collagen protein content decreases. There are no major differences in matrix metabolism between tendons cultured in medium supplemented with FCS or with rhIGF-I only. rhIGF-I may therefore be used as a growth factor supplement in serum-free culture of tendon tissue. IV. Dehydration inhibits in vitro matrix synthesis and cell proliferation in tendon explants. These effects are counteracted by keeping the exposed tendon segments moist with physiological saline solution during preparation. The sensitivity of tendon tissue to dehydration should be considered during tendon surgery. V. Tendon explants, cultured in a diffusion chamber, survive and exhibit an intrinsic capacity for healing. In healing tendon segments incubated for three weeks, protein synthesis remains unchanged and collagen synthesis decreases, whereas the rate of cell proliferation increases as compared with native tendons. VI. Endotenon cells of the rabbit flexor tendon can restore the injured tendon surface and bridge the tendon gap. The rabbit flexor tendon is a morphologically and biochemically heterogeneous tissue with an intrinsic capability for healing. Tendon tissue is susceptible to dehydration and during exposure quickly looses its viability. The metabolic and proliferative capacity of the tendon is stimulated by growth factors and rhIGF-I may be of importance in tendon healing.</p>","PeriodicalId":77378,"journal":{"name":"Scandinavian journal of plastic and reconstructive surgery and hand surgery. Supplementum","volume":"23 ","pages":"1-51"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Scandinavian journal of plastic and reconstructive surgery and hand surgery. Supplementum","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

I. The rabbit flexor tendon within the synovial sheath contains segments with fibrocartilage-like areas. These segments have a higher proteoglycan and a lower collagen and non-collagen protein synthesis compared to the segment with "true" tendon tissue. Cell proliferation is also lower within the proximal segment than in the intermediate and distal segments. These regional variations should be considered when interpreting experimental data. They may also be of importance for the variable healing capacity of different flexor tendon regions. II. Recombinant human insulin-like growth factor, insulin and fetal calf serum stimulate matrix synthesis and cell proliferation in a dose dependent manner in flexor tendon explants cultured for three days. rhIGF-I was more potent than insulin in stimulating cell proliferation and matrix synthesis. rhIGF-I also stimulated matrix synthesis to a higher degree than FCS. III. In long-term culture of flexor tendon explants, the addition of rhIGF-I to the culture medium stimulates matrix synthesis, but does not influence turn-over rates. The total hexosamine and collagen contents in tendons cultured in medium with rhIGF-I remain at the same level, while non-collagen protein content decreases. There are no major differences in matrix metabolism between tendons cultured in medium supplemented with FCS or with rhIGF-I only. rhIGF-I may therefore be used as a growth factor supplement in serum-free culture of tendon tissue. IV. Dehydration inhibits in vitro matrix synthesis and cell proliferation in tendon explants. These effects are counteracted by keeping the exposed tendon segments moist with physiological saline solution during preparation. The sensitivity of tendon tissue to dehydration should be considered during tendon surgery. V. Tendon explants, cultured in a diffusion chamber, survive and exhibit an intrinsic capacity for healing. In healing tendon segments incubated for three weeks, protein synthesis remains unchanged and collagen synthesis decreases, whereas the rate of cell proliferation increases as compared with native tendons. VI. Endotenon cells of the rabbit flexor tendon can restore the injured tendon surface and bridge the tendon gap. The rabbit flexor tendon is a morphologically and biochemically heterogeneous tissue with an intrinsic capability for healing. Tendon tissue is susceptible to dehydration and during exposure quickly looses its viability. The metabolic and proliferative capacity of the tendon is stimulated by growth factors and rhIGF-I may be of importance in tendon healing.

分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
屈肌腱的基质代谢和愈合。兔肌腱的实验研究。
滑膜鞘内的兔屈肌腱包含纤维软骨样区域的节段。与“真正的”肌腱组织相比,这些节段具有较高的蛋白多糖和较低的胶原蛋白和非胶原蛋白合成。细胞增殖在近段内也低于中间和远段。在解释实验数据时应考虑到这些区域差异。它们也可能对不同屈肌腱区域的不同愈合能力很重要。2重组人胰岛素样生长因子、胰岛素和胎牛血清对培养3天的屈肌腱外植体基质合成和细胞增殖具有剂量依赖性。rhigf - 1在刺激细胞增殖和基质合成方面比胰岛素更有效。rhIGF-I对基质合成的刺激程度也高于FCS。3在屈肌腱外植体的长期培养中,在培养基中添加rhigf - 1刺激基质合成,但不影响周转率。在rhigf - 1培养基中培养的肌腱中总己糖胺和胶原蛋白含量保持不变,而非胶原蛋白含量下降。在添加FCS和仅添加rhigf - 1的培养基中培养的肌腱的基质代谢没有明显差异。因此,rhigf - 1可以用作肌腱组织无血清培养中的生长因子补充剂。脱水抑制肌腱外植体的体外基质合成和细胞增殖。这些影响可以通过在准备过程中用生理盐水溶液保持暴露的肌腱段湿润来抵消。在进行肌腱手术时应考虑肌腱组织对脱水的敏感性。在扩散室中培养的肌腱外植体存活并表现出内在的愈合能力。在培养三周的愈合肌腱段中,与天然肌腱相比,蛋白质合成保持不变,胶原合成减少,而细胞增殖率增加。兔屈肌腱内皮细胞可以修复损伤的肌腱表面,桥接肌腱间隙。兔屈肌腱是一种形态和生化异质性的组织,具有内在的愈合能力。肌腱组织容易脱水,暴露后会迅速失去活力。肌腱的代谢和增殖能力受到生长因子的刺激,rhigf - 1可能在肌腱愈合中起重要作用。
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
Craniofacial osteotomies and rigid fixation in the correction of post-traumatic craniofacial deformities. Richard Wilhelm Gottlieb Faltin 1867-1952. Faciocraniosynostosis: from infancy to adulthood. The Göteborg protocol for treatment of craniosynostosis. Personal contributions to craniofacial surgery.
×
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