Zabel M, Schäfer H
Institut of Pathology, University of Hamburg, Federal Republic of Germany.
J Histochem Cytochem. 1988 May;36(5):543-6. doi: 10.1177/36.5.3258608.
By use of appropriate fragments of CT DNA or a CGRP DNA and SP6 polymerase system, we produced anti-sense RNA probes labeled with biotinylated 11-UTP. The labeling and specificity of the RNA probes were confirmed using dot-blot hybridization. By use of hybridocytochemistry, CT mRNA and CGRP mRNA were localized in all parafollicular cells in control and dihydrotachysterin-pre-treated rats. We concluded that all parafollicular cells simultaneously produce both CT mRNA and CGRP mRNA, either under control conditions or after stimulation by dihydrotachysterin-induced hypercalcemia.
通过使用CT DNA或降钙素基因相关肽(CGRP)DNA的合适片段以及SP6聚合酶系统,我们制备了用生物素化的11-UTP标记的反义RNA探针。使用斑点印迹杂交法确认了RNA探针的标记和特异性。通过杂交细胞化学方法,在对照大鼠和二氢速甾醇预处理的大鼠中,降钙素(CT)mRNA和降钙素基因相关肽(CGRP)mRNA定位于所有滤泡旁细胞中。我们得出结论,无论是在对照条件下还是在二氢速甾醇诱导的高钙血症刺激后,所有滤泡旁细胞都同时产生CT mRNA和CGRP mRNA。