284 research outputs found
Promotion of functional heterotrimeric type I collagen via transfection in osteogenesis imperfecta fibroblasts
Abstract only availableOsteogenesis imperfecta (OI) is a heritable disorder due to mutations in type I collagen. Normal type I collagen forms a heterotrimeric protein comprised of two pro1(I) chains and one pro2(I) chain [1(I)22(I)]. The osteogenesis imperfecta murine (oim) model mouse contains a single nucleotide deletion in the pro2(I) gene (COL1A2) resulting in non-functional pro2(I) chains and production of homotrimeric type I collagen containing three pro1(I) collagen chains, [1(I)3], resulting in small body size, increased bone fragility and altered bone mineralization. The overall goal of this study is to correct the oim defect by introducing normal COL1A2 genes into oim cells. Oim dermal fibroblasts were transfected with a series of COL1A2 gene constructs containing the full-length murine pro2(I) collagen cDNA driven by various lengths of the murine COL1A2 promoter (1.5kb, 3.0kb, and 6.0kb) along with a COL1A2 enhancer. These DNA constructs were cotransfected with pcDNA3 containing a neomycin resistance gene, which allows for selection of stably transfected cell lines. Various assays have been developed to monitor proa2(I) collagen expression at the DNA, RNA and protein levels. A PCR assay was used to confirm genomic incorporation of transgenic COL1A2 gene constructs and an RT-PCR assay used to confirm expression of normal pro2(I) collagen mRNA. Denaturing urea-SDS polyacrylamide gel electrophoresis along with Western blotting analyses using anti-murine 1(I) and 2(I) collagen antibodies were used to confirm normal pro2(I) collagen expression at the protein level as well as its incorporation into normal heterotrimeric type I collagen. All the necessary tools have been established for evaluating the efficacy of transfection. Currently, the first series of stably transfected oim cell lines are being expanded for analyses as described above. Although this study is aimed at 'fixing' the oim mutation via gene therapy, valuable data will also be collected regarding the effectiveness of the variable length promoter regions in enhancing the expression of the normal COL1A2 gene.Life Sciences Undergraduate Research Opportunity Progra
Comparison of the progression of glomerulosclerosis between Oim-C57BL/6 and Oim-B6C3Fe a/a [abstract]
Abstract only availableOsteogenesis Imperfecta (OI), a heritable connective tissue disorder, resulting from mutations in the type I procollagen genes is characterized by bone deformity and fragility. The OI mouse model (oim) is homozygous for a null mutation in the COL1A2 gene of type I collagen, displaying a bone phenotype mimicking type III OI in humans. These mice also have glomerulosclerosis characterized by α1(I) homotrimeric type I collagen deposition within their glomeruli. Previous studies in our laboratory demonstrate that oim-B6C3Fe a/a mice exhibit accumulation of glomerular fibrillar collagen beginning post-natally by one week of age, showing increasing severity with continued development. Heterozygous (het) mice have an intermediate glomerular phenotype between homozygous (oim) and wildtype (wt) mice. Although the oim mutation on the C57BL/6 mouse background shows a more severe bone phenotype than its B6C3Fe a/a counterpart, the impact on the glomerular progression and severity is unknown. Preliminary morphometry mapping and lesion scoring data suggest the oim mutation on C57BL/6 and B6C3Fe a/a backgrounds exhibit similar glomerulosclerotic lesion progression between one and four months of age. Het mice of both backgrounds exhibited mild lesions, and little progression of the glomerulopathy beyond one month (0.3075 ± 0.23 and 0.712 ± 0.29 for C57BL/6 and B6C3Fe a/a, respectively). Within oim mice, glomerulosclerosis varies in severity as reflected by a large standard deviation. However, both oim-C57BL/6 and oim-B6C3Fe a/a mouse strains exhibit similar patterns of glomerulosclerotic development with age. One month oim-C57BL/6 mice have less affected glomeruli (1.65 ± 0.55) as compared to oim-B6C3Fe a/a mice (2.1 ± 1.0) suggesting slower progression of disease in oim-C57BL/6, although they reach the same severity by four months of age (3.04 ± 0.4 and 3.29 ± 0.49, respectively). This suggests that regardless of strain, glomerulosclerotic lesions progress similarly, and C57BL/6 mice are appropriate for further studies.CAFNR On Campus Research Internshi
The use of primary dermal fibroblast cultures to evaluate type I collagen expression in the oim model mouse
Abstract only availableOsteogenesis imperfecta type III is a heritable disorder leading to impaired connective tissue function in type I collagen containing tissues including bone fragility, blue-grey sclera, short stature, and hearing loss. Normal type I collagen is a heterotrimeric molecule containing two pro1(I) collagen chains and a similar but genetically distinct pro2(I) collagen chain. The osteogenesis imperfecta murine (oim) model mouse produces only homotrimeric type I collagen due to a single nucleotide deletion in the COL1A2 gene resulting in a non-functional pro2(I) collagen chain. The result is expression of an abnormal type I collagen molecule which leads to the above phenotype. This study is aimed at developing a methodology whereby dermal fibroblast cultures can be utilized for a variety of assays, including type I collagen RNA and protein quantification. For genotype identification, primers flanking the site of the single nucleotide deletion allow for differentiation of wild type, heterozygous and homozygous animals at the genomic level. Upon confirmation, skin was removed from both oim and wildtype mice and the dermal layer harvested. Fibroblasts originating from the dermal layer of each genotype were then cultured and grown to confluence as separate cultures and the RNA and/or protein harvested from both cell types. Total RNA was harvested using the Qiagen RNeasy kit and used to make cDNA, which was then used in conjunction with specific PCR primers to differentiate between wildtype and oim transcripts. For protein studies, the cells were treated with ascorbic acid to maximize the production of collagen prior to harvesting. Type I collagen expression was then confirmed via a western blot using a type I collagen-specific antibody. Initial results indicate the presence of both pro1(I) and pro2(I) collagen chains from harvested wildtype dermal fibroblasts, while media harvested from oim dermal fibroblasts indicated the presence of only the pro1(I) collagen chains. These results confirm the in vivo protein expression profile seen in skin of both oim and wildtype mice is exhibited in vitro in the respective dermal fibroblast cultures. These results will allow us to quantitate pro1(I) and pro2(I) collagen mRNA and protein expression levels. Future experiments will include the quantitation of type I collagen mRNA levels using RT-PCR, as well as the use of densitometry to quantitate type I collagen protein levels by western blot analysis. This in turn promises to provide insight into the mechanism of formation of abnormal type I collagen in the oim model mouse.Life Sciences Undergraduate Research Opportunity Progra
Investigation of type I collagen deposition in the glomeruli of COL1A2 deficient mice
Abstract only availableType I collagen is the most abundant structural protein in the body, playing a major role in the strength and integrity of connective tissues. Alterations in the synthesis and structure of type I collagen result in a number of connective tissue disorders, such as osteogenesis imperfecta and Ehlers-Danlos syndrome. Type I collagen is normally a heterotrimeric type I collagen molecule composed of three pro 1(I) collagen chains and one pro2(I) collagen chain. The COL1A2 deficient mouse produces only homotrimeric molecules, composed of three pro1(I) collagen chains resulting from a functional null mutation in the COL1A2 gene. Recently our lab discovered a novel type I collagen glomerulopathy in the COL1A2 mouse. The novel glomerulopathy demonstrated increased collagen deposition in the renal glomerular mesangium. The collagen accumulation is similar to what is observed in the secondary progression of renal damage, caused by a variety of kidney disorders. This project entails the measurement of COL1A2 and COL1A1 mRNA levels discerning whether increased collagen deposition in the glomeruli mesangium in COL1A2 deficient mice is related to increased type I collagen mRNA expression (pretranslational mechanism). These studies required harvesting kidneys from the COL1A2 deficient, heterozygous, and wildtype mice at one week, two weeks, and one month of age. Total RNA was isolated from harvested kidneys using the Qiagen RNAeasy RNA isolation kit, post mortar and pestle homogenization. The isolated total RNA was then analyzed for amount and quality via spectrophotometer at 260nm and 280nm, and 80ng of total RNA was used for cDNA generation via reverse transcriptase polymerase chain reaction using Promega ImpromII reagents. PCR products were generated for mouse COL1A2 transcripts using primers optimized for Real Time PCR analysis (RT-PCR). Quantitation of the COL1A1 and COL1A2 transcripts was obtained on the Roche LightCycler, with SYBR green monitoring after each amplification cycle. Previous in situ hybridization data suggests that there may not be an increase in mRNA. The study will attempt to gain a greater understanding of the molecular mechanism leading to type I collagen accumulation in the renal mesangium, with future application to understanding the role of extracellular matrix deposition in renal pathology and disease.Life Sciences Undergraduate Research Opportunity Progra
Live Imaging of Type I Collagen Assembly Dynamics in Osteoblasts Stably Expressing GFP and mCherry-Tagged Collagen Constructs
Type I collagen is the most abundant extracellular matrix protein in bone and other connective tissues and plays key roles in normal and pathological bone formation as well as in connective tissue disorders and fibrosis. Although much is known about the collagen biosynthetic pathway and its regulatory steps, the mechanisms by which it is assembled extracellularly are less clear. We have generated GFPtpz and mCherry-tagged collagen fusion constructs for live imaging of type I collagen assembly by replacing the α2(I)-procollagen N-terminal propeptide with GFPtpz or mCherry. These novel imaging probes were stably transfected into MLO-A5 osteoblast-like cells and fibronectin-null mouse embryonic fibroblasts (FN-null-MEFs) and used for imaging type I collagen assembly dynamics and its dependence on fibronectin. Both fusion proteins co-precipitated with α1(I)-collagen and remained intracellular without ascorbate but were assembled into α1(I) collagen-containing extracellular fibrils in the presence of ascorbate. Immunogold-EM confirmed their ultrastuctural localization in banded collagen fibrils. Live cell imaging in stably transfected MLO-A5 cells revealed the highly dynamic nature of collagen assembly and showed that during assembly the fibril networks are continually stretched and contracted due to the underlying cell motion. We also observed that cell-generated forces can physically reshape the collagen fibrils. Using co-cultures of mCherry- and GFPtpz-collagen expressing cells, we show that multiple cells contribute collagen to form collagen fiber bundles. Immuno-EM further showed that individual collagen fibrils can receive contributions of collagen from more than one cell. Live cell imaging in FN-null-MEFs expressing GFPtpz-collagen showed that collagen assembly was both dependent upon and dynamically integrated with fibronectin assembly. These GFP-collagen fusion constructs provide a powerful tool for imaging collagen in living cells and have revealed novel and fundamental insights into the dynamic mechanisms for the extracellular assembly of collagen
Multi-scale Investigation of Weight-bearing Exercise on Bone Biomechanical Integrity in the Osteogenesis Imperfecta Model (oim) Mouse
Comparative Medicine - OneHealth and Comparative Medicine Poster SessionOsteogenesis imperfecta (OI), a heritable connective tissue disorder generally due to type I collagen defects, is characterized by small stature, reduced bone mineral density, and frequent fractures. Bone is inherently mechanosensitive, responding and adapting to its mechanical environment. Bone formation occurs in response to high mechanical loads; often changing its geometry to strengthen the skeleton. In humans, during the normal 2 year prepubertal/pubertal growth period normal children attain 26% of their peak bone mass, and children which are physically active accrue 10-40% more bone (region specific) than inactive children. This suggests that sedentary lifestyle choices of children with OI are particularly detrimental to their bone health. We postulate that even though the OI bone material is biomechanically weaker, the OI bone will respond to exercise (muscle loading and/or gravitational ground force), especially during pubertal growth by altering bone geometry, architecture, and/or mineral:matrix physiochemistry to generate an inherently stronger bone. The potential benefits of therapeutic exercise to OI patients are significant, but the risks are real. It is critical that we first demonstrate the feasibility and potential success of an exercise therapy in a mouse model of OI for it to be considered a viable therapy for patients. To address this need we combined the unique strengths of two University of Missouri Campuses (Columbia and Kansas City) to create a collaborative research team from the Departments of Biochemistry (UMC) and Veterinary Pathobiology (UMC) and Oral Biology (UMKC School of Dentistry) to determine if weight bearing exercise will improve bone biomechanical integrity in a mouse model of osteogenesis imperfecta (oim), and to investigate the molecular, biochemical, physiochemical, structural and biomechanical impact of exercise on bone at the macro-, ultra- and nano-structural levels. The relationship of whole bone biomechanical integrity and geometry to the mineral:matrix composition, architecture, crystal geometry, and the matrix:mineral interactions of bone is poorly understood. Therefore, we examined femurs of wildtype and oim mice by multi-scale analyses characterizing geometry (muCT) and biomechanics (torsional loading to failure) in relation to the bone mineral and matrix, physicochemical and mechanical properties (FTIR, Raman and scanning acoustic microscopy). By muCT and torsional loading to failure we defined the geometric structural properties and the whole bone biomechanical properties (torsional ultimate strength, torsional stiffness, and strain energy until failure), which are a function of both the geometry and bone biomechanical material properties (tensile strength and shear modulus of elasticity). We used FTIR and Raman microscopy in conjunction with scanning acoustic microscopy to correlate the chemical structure and composition with mechanical integrity. We then performed the same analyses on femoral bones from wildtype and oim mice that underwent moderate weight bearing exercise (running on a treadmill) to determine if weight bearing exercise could alter the molecular structure of bone mineral:matrix and improve bone physicochemical and biomechanical properties. Our preliminary findings support the hypothesis that weight bearing exercise induces an adaptive response in oim mouse bone to alter its matrix/mineral composition, physiochemical structure/ property, and geometry to increase bone quality and biomechanical strength
Development of a protocol for the maintenance and mineralization of osteoblasts from oim mice [abstract]
Abstract only availableOsteogenesis imperfecta (OI) is a disease of type I collagen whose hallmark is extreme bone fragility manifested by numerous fractures throughout life. OI is usually caused by decreased amounts of type I collagen and/or the production of abnormal collagen, leading to biomechanically impaired extracellular matrix. Osteoblasts are cells that build the matrix constituents of bone by secreting collagen, which, along with hydroxyapatite crystals, forms the composite structure of bone. It is unclear how osteoblasts respond to a structurally compromised matrix at a cellular level. This project is a pilot study to explore how osteoblasts from the osteogenesis imperfecta mouse (oim) model differ from wildtype osteoblasts, and how these differences contribute to the structurally inferior bone matrix of oim mice. Because there is no established protocol for growing and mineralizing oim osteoblasts in tissue culture, the main focus of my summer research has been developing such a protocol. Osteoblasts were harvested from calvaria taken from oim and wildtype mice at three to four days of age using a trypsin-collagenase solution. The cells were then grown in -MEM in 12-well plates and encouraged to mineralize using -glycerol phosphate and ascorbic acid. Because the outcome measures are protein quantification, fibroblast cultures have been used to help develop the protocols for measuring hydroxyproline, an amino acid unique to collagen, as well as western blotting of type I collagen. While the protocol for growing and mineralizing osteoblasts is still in development, we have finalized our harvesting and plating procedures, allowing to us effectively grow both wildtype and oim osteoblasts in culture
Characterization of muscle in OI Model mice
Abstract only availableOsteogenesis imperfecta (OI) is a congenital connective tissue disorder characterized by decreased bone mineral density and increased bone fragility and susceptibility to fracture. In addition to skeletal fragility, patients with OI reportedly have muscle weakness although currently no systematic evaluation of muscle function or morphology in humans or animal models of the disease has been performed. Normal type I collagen is coded for two genes located on different chromosomes: COL1A1 and COL1A2. The oim/oim mouse is homozygous for a null mutation in the COL1A2 gene and is a phenocopy of human type III OI (severe disease phenotype). Heterozygous mice (oim/+) harbor the null mutation in only one allele of the COL1A2 gene and model human patients with type I OI (mild disease phenotype). We wanted to determine whether the reported muscle weakness in OI patients is due to a muscle pathology. We analyzed the muscle mass, fiber morphology, and cross-sectional area of muscles fibers of the hind limb muscles (quadriceps, gastrocnemius, plantaris, tibialis anterior and soleus), as well as the fiber type composition of the soleus muscle of wildtype (wt), heterozygous (oim/+), and homozygous (oim/oim) mice. Our results demonstrate that the muscle mass/body mass, fiber morphology, cross-sectional area of hindlimb muscles, as well as fiber type composition of the soleus muscle of oim, oim/+ relative to wt (+/+) mouse muscles were not significantly different between the genotypes. We correlated our morphologic findings with a functional contractile assay and determined that muscle tension-force generation and nerve conduction are not impaired in oim/oim or oim/+ mice. These findings suggest that oim and oim/+ mice do not have inherent muscle pathology. This knowledge is important in our ultimate understanding of skeletal muscle in OI model mice and ultimately, humans with this disease.Life Sciences Undergraduate Research Opportunity Progra
Theoretical investigation of a genetic switch for metabolic adaptation
Membrane transporters carry key metabolites across the cell membrane and, from a resource standpoint, are hypothesized to be produced when necessary. The expression of membrane transporters in metabolic pathways is often upregulated by the transporter substrate. In E. coli, such systems include for example the lacY, araFGH, and xylFGH genes, which encode for lactose, arabinose, and xylose transporters, respectively. As a case study of a minimal system, we build a generalizable physical model of the xapABR genetic circuit, which features a regulatory feedback loop via membrane transport (positive feedback) and enzymatic degradation (negative feedback) of an inducer. Dynamical systems analysis and stochastic simulations show that the membrane transport makes the model system bistable in certain parameter regimes. Thus, it serves as a genetic “on-off” switch, enabling the cell to only produce a set of metabolic enzymes when the corresponding metabolite is present in large amounts. We find that the negative feedback from the degradation enzyme does not significantly disturb the positive feedback from the membrane transporter. We investigate hysteresis in the switching and discuss the role of cooperativity and multiple binding sites in the model circuit. Fundamentally, this work explores how a stable genetic switch for a set of enzymes is obtained from transcriptional auto-activation of a membrane transporter through its substrate
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