京都大学 / 0048 / 新制・課程博士 / 博士(薬科学) / 甲第21047号 / 薬科博第90号 / 新制||薬科||10(附属図書館) / 京都大学大学院薬学研究科薬科学専攻 / (主査)教授 竹島 浩, 教授 中山 和久, 教授 金子 周司 / 学位規則第4条第1項該当 / Doctor of Pharmaceutical Sciences / Kyoto University / DFAM

published_or_final_version / abstract / Biochemistry / Doctoral / Doctor of Philosophy

Estudo dos efeitos da irradiação ultra-sônica pulsada de baixa intensidade sobre o desenvolvimento de segmentos da coluna vertebral implantados em camundongos isogênicos / The aim of the present research was evaluate the action of low-intensity pulsed ultrasonic irradiation on development and ossification of vertebral column blastemas, through mice new born tail segments implants in adult receptor isogenic mice lineages C57BL/6 and Balb/C. New born tail segments were implanted in subcutaneous tissues of adults isogenics mice C57BL/6 and intramuscularly in adults isogenics mice Balb/C. After 24 hours the implant, the animals in both groups, were stimulated with the low-intensity pulsed ultrasound (LIPUS), 10 minutes per day. After 5 days of stimulus, the receptors animals were death and had the implanted tails removed for histopathology, trhrough Periodic Acid Schiff plus Alcian Blue (PAS/AB), Masson's tricomico and hem lumen-eosin (HE). The group of animals stimulated which received subcutaneous implant presented the implant with accelerated in inter-vertebral diks, faces to chondrocytes organization and chondroblastes findings in cartilaginous matrix, showing maturity in fiber cartilages arrangements. It was observed too, a collagen fibers enlargement in the disks fibro cartilage which show more dense next the pulposo nucleus in the segments implanted and stimulated, compared with the controls segments. The areas of the segments were available by Fisher's test and Student's t. It didn't watch significant differences in the vertebral bodies' areas sizes in the animals which implant was subcutaneous (p'< OU = '0.05). In the intramuscular implants animals group, it was observed a major velocity in the hialuronic acid matrix formation in the intervertebral disks after LIPUS stimulus. Moreover, the fibrous ring fiber cartilages' were better organized with large number of cells inside the cartilaginous matrix compared with the controls segments. With regard to the vertebral bodies in the intramuscular implants, it's not verifies significant increases in the areas (p'< OU =' 0,05). The findings allow conclude that LIPUS should promote the ontogenetic differentation of the structural components of the mice vertebral column more quickly, trhough vertebras endochondral ossification microscopic evaluation and the inter-vertebral disks components differentiation, follow the methodology employed.

Estrogen-receptor-related receptor gamma, ERRγ, is highly expressed in cartilage and upregulates the chondrogenic transcription factor, Sox9, in a chondrocytic cell line. To assess the effect of increasing ERRγ activity on cartilage in vivo, we generated transgenic animals driving ERRγ expression with a chondrocyte-specific promoter. I verified that one transgenic line exhibited 26% increased ERRγ protein at E14.5. No major morphological defects were seen at this stage, but I observed significant reduction in the size of the appendicular skeleton in P7 mice, such that all elements of the appendicular skeleton were significantly reduced by 4 – 10%. I continued the phenotype analysis at the histological level and found that the P7 animals displayed significantly reduced growth plate height, caused by deficiencies in the size of the proliferative and hypertrophic zones of the growth plate. This suggests a previously unknown role for ERRγ in regulating endochondral ossification in growth plate chondrocytes.

Fracture repair is a regenerative event that involves the precise coordination of a variety of cells for successful healing process. Within the microstructure hierarchy of bone repair, the predominant cells involved include the chondrocytes, osteocytes, osteoblasts, and osteoclasts. Although the role of osteoblasts during fracture healing has been previously shown, their role during the initiation phase of endochondral fracture repair remains unclear. In order to study the role of osteoblasts during fracture repair, we used a transgenic mouse model expressing the herpes simplex virus thymidine kinase gene in early differentiating osteoblasts, which allows conditional ablation of cells in osteoblastic lineage upon treatment with the Gancicolvir drug. Results from this study suggest that not only are osteoblasts required in later stages of fracture repair as the medium for bone synthesis, and osteoclast activation during bone remodelling, but could also be required for the initiation and advancement of the endochondral ossification process.

Estrogen-receptor-related receptor gamma, ERRγ, is highly expressed in cartilage and upregulates the chondrogenic transcription factor, Sox9, in a chondrocytic cell line. To assess the effect of increasing ERRγ activity on cartilage in vivo, we generated transgenic animals driving ERRγ expression with a chondrocyte-specific promoter. I verified that one transgenic line exhibited 26% increased ERRγ protein at E14.5. No major morphological defects were seen at this stage, but I observed significant reduction in the size of the appendicular skeleton in P7 mice, such that all elements of the appendicular skeleton were significantly reduced by 4 – 10%. I continued the phenotype analysis at the histological level and found that the P7 animals displayed significantly reduced growth plate height, caused by deficiencies in the size of the proliferative and hypertrophic zones of the growth plate. This suggests a previously unknown role for ERRγ in regulating endochondral ossification in growth plate chondrocytes.

Fracture repair is a regenerative event that involves the precise coordination of a variety of cells for successful healing process. Within the microstructure hierarchy of bone repair, the predominant cells involved include the chondrocytes, osteocytes, osteoblasts, and osteoclasts. Although the role of osteoblasts during fracture healing has been previously shown, their role during the initiation phase of endochondral fracture repair remains unclear. In order to study the role of osteoblasts during fracture repair, we used a transgenic mouse model expressing the herpes simplex virus thymidine kinase gene in early differentiating osteoblasts, which allows conditional ablation of cells in osteoblastic lineage upon treatment with the Gancicolvir drug. Results from this study suggest that not only are osteoblasts required in later stages of fracture repair as the medium for bone synthesis, and osteoclast activation during bone remodelling, but could also be required for the initiation and advancement of the endochondral ossification process.

Cartilage tissue provides compressive resistance in diarthrodial joints, and has been shown to be regulated by mechanical signals, in particular with regard to production of extracellular matrix proteins. However, less is understood about how chondrocytes in regions not solely purposed to provide compressive resistance may also be affected by mechanical forces. The growth plate is a small layer of cartilage that functions to facilitate longitudinal growth of the long bones from in utero through post-adolescent development. The growth plate maintains distinct regions of chondrocytes at carefully regulated stages of endochondral ossification that are in part characterized by their morphology and differential responsiveness to vitamin D metabolites. Understanding if mechanical cues could be harnessed to accelerate or delay the process of endochondral ossification might be beneficial for optimizing tissue engineering of cartilage or osteochondral interfaces. This study focused on three aims to provide a basis for future work in this area: 1) Develop a cell line culture model useful for studying growth plate chondrocytes, 2) Determine the response of primary growth plate chondrocytes and the cell line model to fluid shear stress, and 3) determine if expression of integrin beta 1 is important for the observed responses to shear stress. The findings of this study suggest that inorganic phosphate can promote differentiation in coordination with the 24,25(OH)2D3 metabolite of vitamin D, and that fluid shear stress generally inhibits differentiation and proliferation of growth plate chondrocytes in part through an integrin beta 1 mediated pathway.

Estudo dos efeitos da irradiação ultra-sônica pulsada de baixa intensidade sobre o desenvolvimento de segmentos da coluna vertebral implantados em camundongos isogênicos / The aim of the present research was evaluate the action of low-intensity pulsed ultrasonic irradiation on development and ossification of vertebral column blastemas, through mice new born tail segments implants in adult receptor isogenic mice lineages C57BL/6 and Balb/C. New born tail segments were implanted in subcutaneous tissues of adults isogenics mice C57BL/6 and intramuscularly in adults isogenics mice Balb/C. After 24 hours the implant, the animals in both groups, were stimulated with the low-intensity pulsed ultrasound (LIPUS), 10 minutes per day. After 5 days of stimulus, the receptors animals were death and had the implanted tails removed for histopathology, trhrough Periodic Acid Schiff plus Alcian Blue (PAS/AB), Masson's tricomico and hem lumen-eosin (HE). The group of animals stimulated which received subcutaneous implant presented the implant with accelerated in inter-vertebral diks, faces to chondrocytes organization and chondroblastes findings in cartilaginous matrix, showing maturity in fiber cartilages arrangements. It was observed too, a collagen fibers enlargement in the disks fibro cartilage which show more dense next the pulposo nucleus in the segments implanted and stimulated, compared with the controls segments. The areas of the segments were available by Fisher's test and Student's t. It didn't watch significant differences in the vertebral bodies' areas sizes in the animals which implant was subcutaneous (p'< OU = '0.05). In the intramuscular implants animals group, it was observed a major velocity in the hialuronic acid matrix formation in the intervertebral disks after LIPUS stimulus. Moreover, the fibrous ring fiber cartilages' were better organized with large number of cells inside the cartilaginous matrix compared with the controls segments. With regard to the vertebral bodies in the intramuscular implants, it's not verifies significant increases in the areas (p'< OU =' 0,05). The findings allow conclude that LIPUS should promote the ontogenetic differentation of the structural components of the mice vertebral column more quickly, trhough vertebras endochondral ossification microscopic evaluation and the inter-vertebral disks components differentiation, follow the methodology employed.

Angiogenesis is required for endochondral ossification during development and fracture healing; however the exact mechanisms and temporal relationship between the two processes remains unclear. In this study, we utilize an in vivo model of endochondral ossification in mice by implanting demineralized bone matrix (DBM) proximal to the femur to induce ectopic bone formation. TNP-470, a drug known to be anti-angiogenic, was used to inhibit vascularization during the time course of de novo bone formation in order to define the role of angiogenesis during the chondrogenic phase of endochondral bone formation. Day 2, day 8, and day 16 post-surgery were selected time points to represent pre-chondrogenic, chondrogenic, and bone mineralization stages, respectively. Plain x-ray and micro-CT analysis showed that inhibition of angiogenesis led to decreased mineralized tissue formation. Inhibited angiogenesis was confirmed with qRT-PCR. Most striking, however, is that while stem cells are recruited and committed to the chondrogenic lineage, subsequent chondrogenesis failed to progress based on the failure of Sox5 and Sox6 expression, which directs chondrocyte commitment. This expands the role for angiogenesis to a much earlier stage than currently thought and places the necessity of angiogenesis very early in the endochondral ossification process.