We have recently developed a model of pancreatic islet transplantation into a decellularized pancreatic tail in rats. As the pancreatic skeletons completely lack endothelial cells, we investigated the effect of co-transplantation of mesenchymal stem cells and endothelial cells to promote revascularization. Decellularized matrix of the pancreatic tail was prepared by perfusion with Triton X-100, sodium dodecyl sulfate and DNase solution. Isolated pancreatic islets were infused into the skeletons via the splenic vein either alone, together with adipose tissue-derived mesenchymal stem cells (adMSCs), or with a combination of adMSCs and rat endothelial cells (rat ECs). Repopulated skeletons were transplanted into the subcutaneous tissue and explanted 9 days later for histological examination. Possible immunomodulatory effects of rat adMSCs on the survival of highly immunogenic green protein-expressing human ECs were also tested after their transplantation beneath the renal capsule. The immunomodulatory effects of adMSCs were also tested in vitro using the Invitrogen Click-iT EdU system. In the presence of adMSCs, the proliferation of splenocytes as a response to phytohaemagglutinin A was reduced by 47% (the stimulation index decreased from 1.7 to 0.9, P = 0.008) and the reaction to human ECs was reduced by 58% (the stimulation index decreased from 1.6 to 0.7, P = 0.03). Histological examination of the explanted skeletons seeded only with the islets showed their partial disintegration and only a rare presence of CD31-positive cells. However, skeletons seeded with a combination of islets and adMSCs showed preserved islet morphology and rich vascularity. In contrast, the addition of syngeneic rat ECs resulted in islet-cell necrosis with only few endothelial cells present. Live green fluorescence-positive endothelial cells transplanted either alone or with adMSCs were not detected beneath the renal capsule. Though the adMSCs significantly reduced in vitro proliferation stimulated by either phytohaemagglutinin A or by xenogeneic human ECs, in vivo co-transplanted adMSCs did not suppress the post-transplant immune response to xenogeneic ECs. Even in the syngeneic model, ECs co-transplantation did not lead to sufficient vascularization in the transplant area. In contrast, islet co-transplantation together with adMSCs successfully promoted the revascularization of extracellular matrix in the subcutaneous tissue.

• MeSH
• decelularizovaná extracelulární matrix MeSH
• endoteliální buňky MeSH
• fyziologická neovaskularizace * MeSH
• krysa rodu rattus MeSH
• kultivované buňky MeSH
• Langerhansovy ostrůvky * imunologie   MeSH
• lidé MeSH
• mezenchymální kmenové buňky * MeSH
• pankreas MeSH
• transplantace Langerhansových ostrůvků * metody   MeSH
• transplantace mezenchymálních kmenových buněk * metody   MeSH
• tuková tkáň * cytologie   MeSH
• zvířata MeSH
• Check Tag
• krysa rodu rattus MeSH
• lidé MeSH
• mužské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH

Exercise induced bone response although established, little is known about the molecular components that mediate bone response to mechanical loading (ML). In our recent QTL study, we identified one such possible molecular component responding to ML: cartilage oligomeric matrix protein (COMP). To address the COMP role in mediating ML effects on bone formation, COMP expression was evaluated as a function of duration and age in response to ML in female B6 mice. A 9N load was applied using a four-point bending device at 2Hz frequency for 36 cycles, once per day for 2-, 4- and 12-days on the right tibia. The left tibia was used as an internal control. Loading caused an increase in COMP expression by 1.3-, 2- and 4-fold respectively after 2-, 4- and 12-days of loading. This increase was also seen in 16 and 36-week old mice. Based on these findings, we next used COMP knockout (KO) mice to evaluate the cause and effect relationship. Quantitative analysis revealed 2 weeks of ML induced changes in vBMD and bone size in the KO mice (5.9 % and 21 % vs. unloaded bones) was not significantly different from control mice (7 % and 24 % vs. unloaded bones). Our results imply that COMP is not a key upstream mediator of the anabolic effects of ML on the skeleton.

• MeSH
• extracelulární matrix - proteiny genetika   metabolismus   MeSH
• glykoproteiny genetika   metabolismus   MeSH
• kosti a kostní tkáň fyziologie   MeSH
• lokus kvantitativního znaku MeSH
• mechanický stres MeSH
• myši knockoutované MeSH
• myši MeSH
• osteogeneze fyziologie   MeSH
• zatížení muskuloskeletálního systému fyziologie   MeSH
• zvířata MeSH
• Check Tag
• myši MeSH
• ženské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• Research Support, U.S. Gov't, Non-P.H.S. MeSH

• MeSH
• achondroplazie etiologie   MeSH
• extracelulární matrix - proteiny MeSH
• geny MeSH
• molekulární biologie MeSH
• mutace MeSH
• Publikační typ
• kongresy MeSH

Infusing pancreatic islets into the portal vein currently represents the preferred approach for islet transplantation, despite considerable loss of islet mass almost immediately after implantation. Therefore, approaches that obviate direct intravascular placement are urgently needed. A promising candidate for extrahepatic placement is the omentum. We aimed to develop an extracellular matrix skeleton from the native pancreas that could provide a microenvironment for islet survival in an omental flap. To that end, we compared different decellularization approaches, including perfusion through the pancreatic duct, gastric artery, portal vein, and a novel method through the splenic vein. Decellularized skeletons were compared for size, residual DNA content, protein composition, histology, electron microscopy, and MR imaging after repopulation with isolated islets. Compared to the other approaches, pancreatic perfusion via the splenic vein provided smaller extracellular matrix skeletons, which facilitated transplantation into the omentum, without compromising other requirements, such as the complete depletion of cellular components and the preservation of pancreatic extracellular proteins. Repeated MR imaging of iron-oxide-labeled pancreatic islets showed that islets maintained their position in vivo for 49 days. Advanced environmental scanning electron microscopy demonstrated that islets remained integrated with the pancreatic skeleton. This novel approach represents a proof-of-concept for long-term transplantation experiments.

• Publikační typ
• časopisecké články MeSH

Cortical bone plays a vital role in determining overall bone strength. We investigate the structural, compositional, and nanomechanical properties of cortical bone following ovariectomy (OVX) of 12-week-old Sprague Dawley rats, since this animal model is frequently employed to evaluate the performance of implantable biomaterials in compromised bone healing conditions. Morphological parameters and material properties of bone in the geometrical center of the femoral cortex were investigated four and eight weeks post-OVX and in unoperated controls (Ctrl), using X-ray micro-computed tomography, backscattered electron scanning electron microscopy, Raman spectroscopy, and nanoindentation. The OVX animals showed increase in body weight, diminished bone mineral density, increased intracortical porosity, but increased bone mass through periosteal apposition (e.g., increases in periosteal perimeter, cortical cross-sectional thickness, and cross-sectional area). However, osteocyte densities, osteocyte lacunar dimensions, and the nanomechanical behavior on the single mineralized collagen fibril level remained unaffected. Our correlative multiscale investigation provides structural, chemical, and nanomechanical evidence substantiating earlier reports suggesting that rats ovariectomized at 12 weeks undergo simultaneous bone loss and growth, resulting in the effects of OVX being less obvious. Periosteal apposition contradicts the conventional view of bone loss in osteoporosis but appears advantageous for the greater functional demand imposed on the skeleton by increased body weight and fragility induced by increased intracortical porosity. Through a variety of morphological changes, it is likely that 12-week-old rats are able to adapt to OVX-related microstructural and compositional alterations. © 2017 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 106A: 997-1007, 2018.

• MeSH
• biomechanika MeSH
• extracelulární matrix metabolismus   MeSH
• femur patologie   patofyziologie   MeSH
• kortikální kost diagnostické zobrazování   patologie   patofyziologie   MeSH
• lineární modely MeSH
• minerály metabolismus   MeSH
• nanočástice chemie   MeSH
• osteocyty metabolismus   MeSH
• osteoporóza diagnostické zobrazování   patologie   patofyziologie   MeSH
• počet buněk MeSH
• poréznost MeSH
• potkani Sprague-Dawley MeSH
• rentgenová mikrotomografie MeSH
• tělesná hmotnost MeSH
• zvířata MeSH
• Check Tag
• ženské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

Activating mutations in fibroblast growth factor receptor 3 (FGFR3) account for the most prevalent form of dwarfism in humans, the achondroplasia. Excessive activation of FGFR3 causes premature chondrocyte growth arrest, abnormal extracellular matrix homeostasis, and altered chondrocyte differentiation, resulting in achondroplasia. Although achondroplasia is considered a curable condition, no treatment is available to date. This is mostly due to our ingnorance of the basic mechanisms governing the FGFR3 signal transduction. Prolonged activation of Erk MAP kinase, mediated by Frs2 adapter protein, is a major effector of FGFR3 activation in achondroplasia. The molecular mechanisms underlying this phenotype are not known. The dynamics of the Frs2 interaction with FGFR3, Erk and other associated proteins holds a key to understanding of pathology of achondroplasia, and will be addressed in this proposal. Via systematic mapping of interactions among FGFR3, Frs2, Erk and other proteins, we aim to identify novel treatment opportunities for achondroplasia.

Aktivující mutace v FGFR3 receptorové tyrozinové kináze způsobují nejrozšířenější formu trpasličího vzrůstu u lidí, achondroplázii. Nadměrná aktivace FGFR3 způsobuje předčasné ukončení růstu chondrocytů, abnormální homeostázu extracelulární matrix a abnormální diferenciaci chondrocytů, vedoucí k achondroplázii. I když je achondroplázie považovaná za léčitelné onemocnění, v současnosti žádná léčba neexistuje. To je především dáno naší neznalostí základních mechanismů, kterými se řídí FGFR3 signální transdukce v chrupavce. Nekontrolovatelná aktivace Erk MAP kinázy, zprostředkovaná signálním adaptérovým proteinem Frs2, představuje hlavní mediátor FGFR3 aktivace u achondroplázie. Molekulární mechanizmy tohoto fenotypu nejsou známy. Dynamika interakce Frs2 s FGFR3, Erk a dalších proteinů představují klíč k pochopení patologie achondroplázie a budou řešena v tomto návrhu. Prostřednictvím systematického mapování interakcí mezi FGFR3, Frs2, Erk a ostaních proteinů budou identifikovány nové možnosti léčby achondroplázie.

• MeSH
• achondroplazie terapie   MeSH
• adaptorové proteiny signální transdukční MeSH
• chondrocyty MeSH
• chrupavka MeSH
• extracelulárním signálem regulované MAP kinasy MeSH
• fosfatasy MeSH
• MAP kinasový signální systém MeSH
• receptor fibroblastových růstových faktorů, typ 3 MeSH
• transformující růstové faktory MeSH

• Konspekt
• Patologie. Klinická medicína
• NLK Obory
• osteologie
• genetika, lékařská genetika
• molekulární biologie, molekulární medicína
• NLK Publikační typ
• závěrečné zprávy o řešení grantu AZV MZ ČR

Achondroplasia is the most prevalent genetic form of dwarfism in humans and is caused by activating mutations in FGFR3 tyrosine kinase. The clinical need for a safe and effective inhibitor of FGFR3 is unmet, leaving achondroplasia currently incurable. Here, we evaluated RBM-007, an RNA aptamer previously developed to neutralize the FGFR3 ligand FGF2, for its activity against FGFR3. In cultured rat chondrocytes or mouse embryonal tibia organ culture, RBM-007 rescued the proliferation arrest, degradation of cartilaginous extracellular matrix, premature senescence, and impaired hypertrophic differentiation induced by FGFR3 signaling. In cartilage xenografts derived from induced pluripotent stem cells from individuals with achondroplasia, RBM-007 rescued impaired chondrocyte differentiation and maturation. When delivered by subcutaneous injection, RBM-007 restored defective skeletal growth in a mouse model of achondroplasia. We thus demonstrate a ligand-trap concept of targeting the cartilage FGFR3 and delineate a potential therapeutic approach for achondroplasia and other FGFR3-related skeletal dysplasias.

• MeSH
• achondroplazie * farmakoterapie   genetika   MeSH
• aptamery nukleotidové * MeSH
• buněčná diferenciace MeSH
• chondrocyty MeSH
• krysa rodu rattus MeSH
• myši MeSH
• receptor fibroblastových růstových faktorů, typ 3 genetika   MeSH
• vývoj kostí MeSH
• zvířata MeSH
• Check Tag
• krysa rodu rattus MeSH
• myši MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH

BACKGROUND: Beyond its structural role in the skeleton, the extracellular matrix (ECM), particularly basement membrane proteins, facilitates communication with intracellular signaling pathways and cell to cell interactions to control differentiation, proliferation, migration and survival. Alterations in extracellular proteins cause a number of skeletal disorders, yet the consequences of an abnormal ECM on cellular communication remains less well understood METHODS: Clinical and radiographic examinations defined the phenotype in this unappreciated bent bone skeletal disorder. Exome analysis identified the genetic alteration, confirmed by Sanger sequencing. Quantitative PCR, western blot analyses, immunohistochemistry, luciferase assay for WNT signaling were employed to determine RNA, proteins levels and localization, and dissect out the underlying cell signaling abnormalities.  Migration and wound healing assays examined cell migration properties. FINDINGS: This bent bone dysplasia resulted from biallelic mutations in LAMA5, the gene encoding the alpha-5 laminin basement membrane protein. This finding uncovered a mechanism of disease driven by ECM-cell interactions between alpha-5-containing laminins, and integrin-mediated focal adhesion signaling, particularly in cartilage. Loss of LAMA5 altered β1 integrin signaling through the non-canonical kinase PYK2 and the skeletal enriched SRC kinase, FYN. Loss of LAMA5 negatively impacted the actin cytoskeleton, vinculin localization, and WNT signaling. INTERPRETATION: This newly described mechanism revealed a LAMA5-β1 Integrin-PYK2-FYN focal adhesion complex that regulates skeletogenesis, impacted WNT signaling and, when dysregulated, produced a distinct skeletal disorder. FUNDING: Supported by NIH awards R01 AR066124, R01 DE019567, R01 HD070394, and U54HG006493, and Czech Republic grants INTER-ACTION LTAUSA19030, V18-08-00567 and GA19-20123S.

• MeSH
• alely * MeSH
• buněčná adheze genetika   MeSH
• chondrocyty metabolismus   MeSH
• fenotyp MeSH
• fokální adhezní kinasa 2 genetika   metabolismus   MeSH
• genetická predispozice k nemoci MeSH
• genetické asociační studie MeSH
• kosti a kostní tkáň abnormality   diagnostické zobrazování   MeSH
• laminin genetika   metabolismus   MeSH
• lidé MeSH
• mutace * MeSH
• mutační analýza DNA MeSH
• signální dráha Wnt MeSH
• signální transdukce * MeSH
• skupina kinas odvozených od src-genu metabolismus   MeSH
• vývojové onemocnění kostí diagnóza   etiologie   metabolismus   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH

Decellularized scaffolds can serve as an excellent three-dimensional environment for cell repopulation. They maintain tissue-specific microarchitecture of extracellular matrix proteins with important spatial cues for cell adhesion, migration, growth, and differentiation. However, criteria for quality assessment of the three-dimensional structure of decellularized scaffolds are rather fragmented, usually study-specific, and mostly semi-quantitative. Thus, we aimed to develop a robust structural assessment system for decellularized porcine liver scaffolds. Five scaffolds of different quality were used to establish the new evaluation system. We combined conventional semi-quantitative scoring criteria with a quantitative scaffold evaluation based on automated image analysis. For the quantitation, we developed a specific open source software tool (ScaffAn) applying algorithms designed for texture analysis, segmentation, and skeletonization. ScaffAn calculates selected parameters characterizing structural features of porcine liver scaffolds such as the sinusoidal network. After evaluating individual scaffolds, the total scores predicted scaffold interaction with cells in terms of cell adhesion. Higher scores corresponded to higher numbers of cells attached to the scaffolds. Moreover, our analysis revealed that the conventional system could not identify fine differences between good quality scaffolds while the additional use of ScaffAn allowed discrimination. This led us to the conclusion that only using the combined score resulted in the best discrimination between different quality scaffolds. Overall, our newly defined evaluation system has the potential to select the liver scaffolds most suitable for recellularization, and can represent a step toward better success in liver tissue engineering.

• Publikační typ
• časopisecké články MeSH