Spooner B S, Bassett K, Stokes B
Dev Biol. 1985 May;109(1):177-83. doi: 10.1016/0012-1606(85)90358-6.
We investigated whether the inhibition of proteoglycan synthesis and salivary branching morphogenesis by beta-D-xyloside was related to the deposition and processing of newly synthesized glycosaminoglycans at the basal epithelial surface that correlates with normal branching activity. Forty eight-hour cultures of control and 0.5 mM beta-xyloside-treated submandibular rudiments were labeled for 2 hr with [35S]sulfate and fixed and processed for autoradiography, immediately or after 2, 4, 6, or 8 hr of postlabeling chase in nonradioactive medium. The data demonstrated that deposition of chondroitin sulfate-rich material at the basal epithelial surface was strikingly reduced in beta-xyloside-treated rudiments, while patterns of label loss during postlabeling chase were not altered.
我们研究了β-D-木糖苷对蛋白聚糖合成和唾液腺分支形态发生的抑制作用是否与新合成的糖胺聚糖在基底上皮表面的沉积和加工有关,而这种沉积和加工与正常的分支活动相关。用[35S]硫酸盐对对照组和经0.5 mM β-木糖苷处理的下颌下原基进行48小时培养,标记2小时,然后立即或在非放射性培养基中进行2、4、6或8小时的标记后追踪,之后固定并进行放射自显影处理。数据表明,在经β-木糖苷处理的原基中,基底上皮表面富含硫酸软骨素的物质沉积显著减少,而标记后追踪期间的标记丢失模式没有改变。