RESUMO
Osteoporosis is widely viewed as a major public health concern, but the exact magnitude of the problem is uncertain. MicroRNAs play a key role in maintaining bone development and metabolism. This study aims to investigate the effects that microRNA-874 (miR-874) has on osteoblast proliferation and differentiation in osteoporosis rats by targeting SUFU through the Hedgehog signaling pathway. Twenty Wistar female rats were selected for following experiment, and another 20 rats were served as the normal group. Their osteogenic tissues were obtained and the positive expression of SUFU in tissues was determined. Rat osteoblasts were isolated and. The targeting relationship between SUFU and miR-874 was verified and the expression of miR-874, SUFU, Sonic Hedgehog (Shh), Ptch, Smoothened (Smo), bone morphogenetic protein (BMP2), Runx2, proliferating cell nuclear antigen (PCNA) and Bcl-2 associated X protein (Bax) were identified. Besides, cell viability apoptosis, and differentiation were confirmed respectively. Moreover, calcium nodules were observed. Overexpression of SUFU and Bax but lower expression of miR-874, Shh, Ptch, Smo, BMP2, Runx2, and PCNA were found in osteoporosis mice. Besides, elevated expression of miR-874, Shh, Ptch, Smo, BMP2, Runx2 and PCNA, as well as increased cell viability, ALP activity and calcium nodules but decreased expression of SUFU and Bax, and reduced cell apoptosis were confirmed when treated with miR-874 mimic. And it is reciprocal when miR-874 was inhibited. Our study demonstrated that through targeted inhibition of SUFU and activation of Hedgehog signaling pathway, miR-874 could promote the proliferation and differentiation of osteoblasts in osteoporosis rats.
Assuntos
Proteínas Hedgehog/metabolismo , MicroRNAs/fisiologia , Osteoblastos/citologia , Osteoporose/patologia , Proteínas Repressoras/antagonistas & inibidores , Animais , Apoptose , Diferenciação Celular , Proliferação de Células , Feminino , Osteoporose/metabolismo , Ratos , Ratos Wistar , Proteínas Repressoras/análise , Transdução de SinaisRESUMO
Crosstalk between subchondral bone and articular cartilage is considered a central feature of osteoarthritis (OA) initiation and progression, but its underlying molecular mechanism remains elusive. Meanwhile, specific administration of drugs in subchondral bone is also a great challenge during investigation of the process. We here explore the role of stromal cell-derived factor 1 (SDF-1)/C-X-C chemokine receptor type 4 (CXCR4) axis in the crosstalk between subchondral bone and articular cartilage in OA pathogenesis, using osmotic infusion pumps implanted in tibial subchondral bone directly to ensure quantitative, continuous and steady drug delivery over the entire experiment. We found that increased SDF-1 in subchondral bone firstly induced subchondral bone deterioration by erroneous Mesenchymal Stem Cells (MSCs) recruitment and excessive bone resorption in anterior cruciate ligament transection (ACLT) mice. Deterioration of subchondral bone then led to the traverse of SDF-1 from subchondral bone to overlying cartilage. Finally, SDF-1 from underlying subchondral bone combined with CXCR4 in chondrocytes to induce articular cartilage degradation by promoting the shift of transforming growth factor-ß receptor type I (TßRI) in chondrocytes from activin receptor-like kinase 5 (ALK5) to activin receptor-like kinase 1 (ALK1). More importantly, specific inhibition of SDF-1/CXCR4 axis in ACLT rats attenuated OA by stabilizing subchondral bone microarchitecture, reducing SDF-1 in cartilage and abrogating the shift of TßRI in chondrocytes. Our data demonstrate that the SDF-1/CXCR4 axis may coordinate the crosstalk between subchondral bone and articular cartilage in OA pathogenesis. Therefore, specific inhibition of SDF-1/CXCR4 axis in subchondral bone or intervention in SDF-1 traverse may be therapeutic targets for OA.
Assuntos
Cartilagem Articular/citologia , Cartilagem Articular/metabolismo , Quimiocina CXCL12/metabolismo , Osteoartrite do Joelho/metabolismo , Osteoartrite do Joelho/patologia , Receptores CXCR4/metabolismo , Animais , Western Blotting , Cartilagem Articular/patologia , Quimiocina CXCL12/genética , Imuno-Histoquímica , Hibridização in Situ Fluorescente , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Ratos , Ratos Sprague-Dawley , Receptores CXCR4/genéticaRESUMO
AIM: To study the role of the caudate-putamen (CPu)-hippocampus (HPC)-medial temporal lobe neocortex (MTNC) neural pathway in re-establishment of pathophysiological neural networks related to epileptogenesis. METHODS: Experiments were performed under anaesthesia on 45 SD rats. The right HPC, the right MTNC, bilateral HPC, the right HPC and the right MTNC depth electrographs were recorded with bipolar concentric electrodes. Tetanization (60 Hz, 2 s, 0.4 - 0.6 mA) of the right CPu or of the right HPC trains were used to establish acute rat epilepsy model. These depth electrographs were detected before or after tetani were delivered about 10 times at 10 min intervals. RESULTS: Tetanization of the right CPu induced (1) primary afterdischarges and unilateral or bilateral HPC electrographic afterdischarges and kindling effect or inhibition-rebound-kindling effect were induced by repetitive tetani into the right CPu. (2) After injection of scopolamine (0.05 mg/kg i.p.), 3 Hz slow oscillations in HPC electrographs exhibited long-term potentiation followed by repetitive tetani into the right CPu. (3) After administration of scopolamine (i.p.) electrographic oscillations at 3Hz with synaptic modification in bilateral HPC were induced and epileptiform activities in the RHPC were synchronized with those in the RMTNC. CONCLUSION: Pathophysiological neural networks from the Cpu into the HPC might be reestablished by overactivation of the right CPu, in which two hemispheres are involved while temporal lobe epileptogenesis was facilitated.
Assuntos
Hipocampo/fisiologia , Neocórtex/fisiologia , Vias Neurais , Lobo Temporal/fisiologia , Animais , Núcleo Caudado/fisiologia , Estimulação Elétrica , Masculino , Putamen/fisiologia , Ratos , Ratos Sprague-DawleyRESUMO
AIM: To study the role of epileptic neural networks reestablished in contralateral caudate putamen (CPu)-hippocampus(HPC) by using chronic tetanization of the right corpus callosum (CTRCC). METHODS: Experiments were performed on 50 SD rats under anaesthesia. The left CPu (LCPu) and the left HPC(LHPC) electrographs were synchronously recorded after acute tetanization following CTRCC (60 Hz, 0.4-0.6 mA, 2 s). RESULTS: (1) In contralateralization to the side implanted interconvertible network inhibition between the CPu and the HPC were induced by combinedly using chronic and acute tetanization of the RCC. (2) Electrographic kindling in the LCPu or in the LHPC was recorded after CTRCC. (3) In case the LCPu or the LHPC electrographs were not kindled after CTRCC, hypsarrhythmia in the LCPu and reduced sharp waves in the HPC were induced b y repetitive tetanization of the RCC once again. Primary afterdischarges in the LCPu or in the LHPC electrographs were evoked by combinedly using chronic and acute tetanization of the RCC. CONCLUSION: Pathophysiological neural networks in the CPu and in the HPC might be reestablished in another side of hemispheres by chronic over-activation of the right CC, which is related to epileptogenesis. Abnormal interactions between the two functional neural networks might be involved in formation of secondary epileptic focus.
Assuntos
Núcleo Caudado/fisiopatologia , Corpo Caloso/patologia , Epilepsia/patologia , Hipocampo/fisiopatologia , Rede Nervosa , Animais , Núcleo Caudado/patologia , Corpo Caloso/fisiopatologia , Modelos Animais de Doenças , Estimulação Elétrica , Epilepsia/fisiopatologia , Hipocampo/patologia , Masculino , Putamen/patologia , Putamen/fisiopatologia , Ratos , Ratos Sprague-DawleyRESUMO
AIM: The electrographic and behavioral kindling effects were induced by chronic tetanization of the right caudate-putamen (CPu) to study the target-behavior expression involved in the CPu or hippocampus (HPC) network abnormalities. METHODS: Experiments were performed on 58 SD rats. Tetanization (60Hz,0.4 - 0.6mA, 2s) was delivered into the CPu or the HPC, once a day, for 7-12 days. Animal behaviors were observed every day and depth electrographs were recorded at the beginning or at the end of the experiments. RESULTS: Chronic tetanization of the CPu or of the HPC induced: (1) Rhythmic sharp waves in the CPu and paroxysmal epileptiform events in the HPC electrographs. (2) Primary behavioral seizures, secondary behavioral seizures, and kindling effects, including wet dog shakes (WEDS), rearing, face washing, immobility, chewing and head nodding. (3) Lower rate of primary WEDS (P < 0.01), and higher rate of secondary WEDS (P < 0.01) in the CPu-tetanized rats. (4) Longer silent period of behavioral seizures before kindling appeared in the CPu-tetanized rats. CONCLUSION: Kindling effects in the CPu-tetanized rats resembles those in the HPC-tetanized rats. The CPu might participate in the origin of epileptic focus and be involved in reestablishment of limbic epileptic networks, which may be responsible for the target-behavioral seizures.