Immunolocalization of Enzymes/Membrane Transporters Related to Bone Mineralization in the Metaphyses of the Long Bones of Parathyroid-Hormone-Administered Mice

التفاصيل البيبلوغرافية
العنوان: Immunolocalization of Enzymes/Membrane Transporters Related to Bone Mineralization in the Metaphyses of the Long Bones of Parathyroid-Hormone-Administered Mice
المؤلفون: Amizuka, Takahito Mae, Tomoka Hasegawa, Hiromi Hongo, Tomomaya Yamamoto, Shen Zhao, Minqi Li, Yutaka Yamazaki, Norio
المصدر: Medicina; Volume 59; Issue 6; Pages: 1179
بيانات النشر: Multidisciplinary Digital Publishing Institute, 2023.
سنة النشر: 2023
مصطلحات موضوعية: mineralization, parathyroid hormone, ENPP1, TNALP, PHEX, MEPE
الوصف: The present study aimed to demonstrate the immunolocalization and/or gene expressions of the enzymes and membrane transporters involved in bone mineralization after the intermittent administration of parathyroid hormone (PTH). The study especially focused on TNALP, ENPP1, and PHOSPHO1, which are involved in matrix vesicle-mediated mineralization, as well as PHEX and the SIBLING family, which regulate mineralization deep inside bone. Six-week-old male mice were subcutaneously injected with 20 μg/kg/day of human PTH (1–34) two times per day (n = 6) or four times per day (n = 6) for two weeks. Additionally, control mice (n = 6) received a vehicle. Consistently with an increase in the volume of the femoral trabeculae, the mineral appositional rate increased after PTH administration. The areas positive for PHOSPHO1, TNALP, and ENPP1 in the femoral metaphyses expanded, and the gene expressions assessed by real-time PCR were elevated in PTH-administered specimens when compared with the findings in control specimens. The immunoreactivity and/or gene expressions of PHEX and the SIBLING family (MEPE, osteopontin, and DMP1) significantly increased after PTH administration. For example, MEPE immunoreactivity was evident in some osteocytes in PTH-administered specimens but was hardly observed in control specimens. In contrast, mRNA encoding cathepsin B was significantly reduced. Therefore, the bone matrix deep inside might be further mineralized by PHEX/SIBLING family after PTH administration. In summary, it is likely that PTH accelerates mineralization to maintain a balance with elevated matrix synthesis, presumably by mediating TNALP/ENPP1 cooperation and stimulating PHEX/SIBLING family expression.
وصف الملف: application/pdf
اللغة: English
تدمد: 1648-9144
DOI: 10.3390/medicina59061179
URL الوصول: https://explore.openaire.eu/search/publication?articleId=multidiscipl::34da4a53ae9c1f3f3a3b27fbc863b307
حقوق: OPEN
رقم الأكسشن: edsair.multidiscipl..34da4a53ae9c1f3f3a3b27fbc863b307
قاعدة البيانات: OpenAIRE
الوصف
تدمد:16489144
DOI:10.3390/medicina59061179