BBP (Bone Morphogenetic Protein Binding Peptide) and Bone Healing

BBP（骨形态发生蛋白结合肽）和骨愈合

• 批准号: 8040794
• 负责人: SAMUEL Scott MURRAY
• 金额: --
• 依托单位: VA GREATER LOS ANGELES HEALTHCARE SYSTEM
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-10-01 至 2014-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8040794
• 关键词: Accounting; Adverse effects; Affect; Affinity; Amino Acid Substitution; Amino Acids; Apatites; Attenuated; Binding; Binding Proteins; Biochemical; Biological; Biological Assay; Bone Growth; Bone Matrix; Bone Morphogenetic Proteins; Bone Transplantation; C-terminal; Cartilage; Cell Proliferation; Cells; Characteristics; Charge; Chemicals; Chondrocytes; Chondrogenesis; Clinical; Collagen; Complex; Cyclic Peptides; Defect; Development; Diffusion; Dose; Embryonic Development; Engineering; Equilibrium; Exhibits; Extracellular Matrix Proteins; Family; Fracture; Fracture Healing; Gene Expression; Gene Expression Regulation; Growth Factor; Healed; Histology; Human; Immobilization; Implant; Individual; Inflammation; Joints; Kinetics; Lead; Length; Ligands; MAP Kinase Gene; MAPK14 gene; MAPK8 gene; Mediating; Mesenchymal; Minerals; Modification; Mutation; Nuclear Translocation; Orthopedic Surgery procedures; Orthopedics; Osteoblasts; Osteocalcin; Osteogenesis; Outcome; Pathway interactions; Peptides; Phospho-Specific Antibodies; Phosphorylation; Phosphotransferases; Play; Proliferating; Property; Protein Binding; Proteins; Proteoglycan; Proteolysis; Receptor Signaling; Recombinants; Regulation; Relative (related person); Reporting; Research; Rodent Model; Role; Scanning; Signal Transduction; Site; Skeleton; Spinal Canal; Spinal Fusion; Stream; Surface Plasmon Resonance; Testing; Therapeutic; Therapeutic Agents; Time; Tissues; Transforming Growth Factor Beta 2; Transforming Growth Factor beta; Transforming Growth Factors; Translating; Trauma; Veterans; Water; attenuation; base; bone; bone growth factor; bone healing; bone metabolism; bone morphogenetic protein 2; bone morphogenetic protein 7; cancer surgery; carcinogenesis; casein kinase II; cathelicidin; cell growth; clinically relevant; combat; cost; cytokine; design; disulfide bond; extracellular; healing; human TGFB1 protein; improved; injured; insight; intramembranous bone formation; long bone; member; neoplastic cell; novel; osteogenic; receptor; receptor binding; reconstruction; release factor; secreted phosphoprotein 24; skeletal; synthetic peptide; theories

DESCRIPTION (provided by applicant): Many TGF-b (transforming growth factor)/BMP (bone morphogenetic protein) cytokines stimulate pluripotent mesenchymal cells to proliferate and differentiate into the chondrocytes and osteoblasts that elaborate cartilage and bone. Recombinant human BMPs (rhBMPs) are used in orthopedic surgery, but they are expensive, water-soluble, and exhibit short retention times. Cortical bone contains the tiny amount of BMP required to initiate fracture healing, but the amount of rhBMP required to induce bone formation is much greater. Wozney, et al., postulated that demineralized bone matrix (DBM) contains something that "contributes slow release/immobilization characteristics to BMP", thus "reducing the amount of BMP needed" to stimulate osteogenesis. DBM contains secreted phosphoprotein-24 kDa (spp24), a proteolytically-labile protein that contains both mineral- and TGF-b/BMP cytokine-binding domains, which may account for slow release. FL (full-length)-spp24 and its degradation products (i.e., spp18.1, spp16, and spp14.5) bind BMP-2 and -7. Only FL-spp24 (but not its truncated derivatives) binds TGF-b2, suggesting that spp24 proteolysis results in products that differentially bind BMP and TGF-b. Differential binding could modulate the relative availability of TGF-bs vs. BMPs and may contribute to the regulation of bone metabolism. FL-spp24 contains 2 BMP-binding domains (the TRH1 or TGF-b receptor II homology-1 domain and a novel C-terminal domain), but spp24 degradation products contain only 1 BMP-binding domain (the TRH1 domain), which may account for the difference in BMP and TGF-b binding. The Cys1-to- Cys19 disulfide-bonded synthetic peptide corresponding to the TRH1 domain of spp24 is called cyclic BMP binding peptide (cBBP). cBBP increases the tissue retention of BMP-2 and stimulates BMP-2 and BMP-7- mediated spinal fusion and BMP-2-mediated long bone healing. In theory, the BMP-binding properties of cBBP make it an ideal candidate for a BMP carrier in SBGS (synthetic bone graft substitutes). The long-term objectives of our research are to: (1) determine the roles of spp24 and its degradation products in the regulation of TGF-b cytokine superfamily activity in bone, and (2) design improved cBBP derivatives for use in SBGS. We will test hypotheses that: (a) FL-spp24 binding to TGF-bs inhibits the interaction between TGF-bs and their receptors and attenuates down-stream, post-receptor Smad- dependent and -independent signaling and gene regulation, and (b) chemical modifications of cBBP that decrease its KD (increase its "affinity") for BMP or increase the negative charge on cBBP to permit it to bind the positively-charged BMPs more effectively will promote BMP retention and enhance cytokine bioactivity in SBGS. In Specific Aim 1, we will determine the effects of C-terminal degradation of spp24 on the kinetics of its binding to TGF-bs by SPR (surface plasmon resonance) and competitive receptor binding assay. In Specific Aim 2, we will determine the effects of spp24 degradation on TGF-b signal transduction mediated by Smad-dependent pathways, assessed as R-Smad phosphorylation and nuclear translocation. In Specific Aim 3, we will determine the effects of spp24 degradation on Smad-independent MAPK, JNK, ERK and p38 kinase pathways in TGF-b-treated cells, based on quantitative analysis of phospho-specific antibody arrays. The results will be validated by qPCR of TGF-b-mediated gene expression. In Specific Aim 4, we will determine the effects of spp24 degradation on TGF-b-induced intramembranous bone formation and chondrogenesis by quantitative histology and immunohistology of types I and II collagen and osteocalcin. In Specific Aim 5, we will synthesize cBBP derivatives with decreased KDs (increased affinities) for BMPs or which are chemically phosphorylated to increase their BMP-binding capacity. Their binding to BMPs will be assessed by SPR, and their effects on BMP-2 and -7 bioactivity will be determined in the ectopic bone forming bioassay, with confirmation in a rodent model of bone healing, such as spinal fusion. PUBLIC HEALTH RELEVANCE: The clinical relevance of this project is direct because the object is to produce materials that can be translated into therapeutics. Complex fractures, non-unions, and large bone defects due to trauma or cancer surgery that require extensive reconstruction are common problems among both veterans and combat injured individuals. Our long-term objective is to develop less expensive, more effective synthetic bone graft substitutes for use in orthopedic applications. We hope to develop a family of bone growth factor or BMP/TGF-b (bone morphogenetic protein/transforming growth factor-beta)-binding materials that can be employed in clinical situations where there is a need to retain the growth factors at the skeletal site where they are implanted in order to enhance their activity and promote bone growth and the successful integration of bone grafts or artificial joints into the skeleton. We will also determine how the native bone protein spp24 (secreted phosphoprotein-24 kDa) inhibits BMP/TGF-b-dependent tumor cell growth.

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