Zhuang Y H, Bläuer M, Pelto-Huikko M, Syvälä H, Tuohimaa P
Department of Anatomy, Medical School, University of Tampere, Finland.
Histochem Cell Biol. 1996 Sep;106(3):311-8. doi: 10.1007/BF02473241.
Retinoic acid (RA), through its cognate receptors (retinoic acid receptors, RARs), plays an important role in the ontogenesis and maintenance of the normal function of murine Harderian and submandibular glands. In the present study, autoradiography was used to study RA binding to these glands. Both glands showed high radioactive labelling after [14C]-RA administration in normal and partially vitamin A-deficient (VAD) mice. The peak uptake was at 6 h after [14C]-RA administration in normal mice and at 0.5 h in VAD mice. At 24 h, RA binding remained high in normal mice, while it decreased significantly in VAD mice. In western blots with an antibody recognizing all forms of RARs, a band of molecular weight 51 kDa was seen in homogenates of both glands. Immunohistochemically, RAR staining was found in the nuclei of the glandular cells. The Harderian gland exhibited more intense staining than the submandibular gland. In the latter, the most intense staining was seen in the acinar cells, followed by the intercalated duct cells. The granular convoluted tubule showed weak immunostaining and the striated duct was negative. In the Harderian gland, RAR immunostaining was observed in both type I and II cells, but only part of them stained with RAR antibody. The expression of RAR alpha, beta, and gamma transcripts was studied by in situ hybridization using specific oligonucleotide probes. The cell-specific expression of RAR alpha mRNA in the submandibular gland corresponded to the RAR proteins detected by immunohistochemistry, while the RAR beta transcript was mainly seen in the striated duct. The transcripts of RAR alpha and beta were evenly distributed in type I and II glandular cells of the Harderian gland. RAR gamma labelling was below detectable levels in both glands. This result suggests that RA and RARs regulate the functions of Harderian and submandibular glands in a cell-specific manner.
视黄酸(RA)通过其同源受体(视黄酸受体,RARs)在小鼠哈德氏腺和下颌下腺的个体发生及正常功能维持中发挥重要作用。在本研究中,采用放射自显影术研究RA与这些腺体的结合情况。在正常及部分维生素A缺乏(VAD)小鼠中给予[14C]-RA后,两种腺体均显示出高放射性标记。正常小鼠在给予[14C]-RA后6小时摄取量达到峰值,而VAD小鼠在0.5小时达到峰值。24小时时,正常小鼠的RA结合仍保持高水平,而VAD小鼠则显著下降。在用识别所有形式RARs的抗体进行的蛋白质免疫印迹中,在两种腺体的匀浆中均可见一条分子量为51 kDa的条带。免疫组织化学显示,在腺细胞的细胞核中发现了RAR染色。哈德氏腺的染色比下颌下腺更强烈。在下颌下腺中,腺泡细胞染色最强,其次是闰管细胞。颗粒曲管显示弱阳性,纹状管为阴性。在哈德氏腺中,I型和II型细胞均观察到RAR免疫染色,但只有部分细胞被RAR抗体染色。使用特异性寡核苷酸探针通过原位杂交研究RARα、β和γ转录本的表达。下颌下腺中RARα mRNA的细胞特异性表达与免疫组织化学检测到的RAR蛋白相对应,而RARβ转录本主要见于纹状管。RARα和β的转录本在哈德氏腺的I型和II型腺细胞中均匀分布。两种腺体中RARγ标记均低于可检测水平。这一结果表明,RA和RARs以细胞特异性方式调节哈德氏腺和下颌下腺的功能。