{"id":{"repo_id":"loma-linda","oai_identifier":"oai:scholarsrepository.llu.edu:etd-1039"},"canonical_url":"https://search.dev.ndltd.org/etd/loma-linda/oai:scholarsrepository.llu.edu:etd-1039","repository":{"repo_id":"loma-linda","name":"Loma Linda University","base_url":"https://scholarsrepository.llu.edu/do/oai/"},"display":{"title":"Novel Molecules that Regulate Bone Formation and Bone Resorption","abstract":"Osteoporosis is a disease characterized by decreased bone mass and microarchitectural deterioration of bone. Bone loss occurs when the increased bone resorption that occurs with age is not compensated by a corresponding increase in bone formation. Therefore, understanding the mechanisms which regulate bone formation and bone resorption is important for developing diagnostic and treatment strategies for osteoporosis. In my dissertation, we investigated the role of Glutaredoxin 5 (Grx5), Diabetes and Obesity Related protein (DOR), and Claudin 18 (Cldn-18), novel molecules involved in regulating bone formation and bone resorption. We demonstrated that Grx5 protects osteoblasts from oxidative stress induced apoptosis via a molecular pathway that involves regulation of reactive oxygen species production, cardiolipin oxidation, caspase activity, iron-sulfur cluster formation, and manganese superoxide dismutase activity. We found that DOR is an important regulator of osteoblast differentiation. In addition, a single nucleotide polymorphism (SNP) in the promoter of human DOR gene associated with plasma levels of the bone formation marker, osteocalcin, in men. Targeted disruption of the tight junction protein, Cldn-18, in mice led to significant deficits in peak bone mass due to increased bone resorption with no effect on bone formation. Cldn-18 is a novel negative regulator of osteoclast differentiation that interacts with ZO-2 to modulate RANKL signaling in osteoclasts. Collectively, these findings may provide insight into the molecular mechanisms which regulate bone formation and bone resorption, and may be useful in developing therapeutic strategies to prevent low bone mass.","abstract_html":"Osteoporosis is a disease characterized by decreased bone mass and microarchitectural deterioration of bone. Bone loss occurs when the increased bone resorption that occurs with age is not compensated by a corresponding increase in bone formation. Therefore, understanding the mechanisms which regulate bone formation and bone resorption is important for developing diagnostic and treatment strategies for osteoporosis. In my dissertation, we investigated the role of Glutaredoxin 5 (Grx5), Diabetes and Obesity Related protein (DOR), and Claudin 18 (Cldn-18), novel molecules involved in regulating bone formation and bone resorption. We demonstrated that Grx5 protects osteoblasts from oxidative stress induced apoptosis via a molecular pathway that involves regulation of reactive oxygen species production, cardiolipin oxidation, caspase activity, iron-sulfur cluster formation, and manganese superoxide dismutase activity. We found that DOR is an important regulator of osteoblast differentiation. In addition, a single nucleotide polymorphism (SNP) in the promoter of human DOR gene associated with plasma levels of the bone formation marker, osteocalcin, in men. Targeted disruption of the tight junction protein, Cldn-18, in mice led to significant deficits in peak bone mass due to increased bone resorption with no effect on bone formation. Cldn-18 is a novel negative regulator of osteoclast differentiation that interacts with ZO-2 to modulate RANKL signaling in osteoclasts. Collectively, these findings may provide insight into the molecular mechanisms which regulate bone formation and bone resorption, and may be useful in developing therapeutic strategies to prevent low bone mass.","abstract_has_math":false,"creators":["Linares, Gabriel Robert"],"institution":null,"degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation","degree_discipline":"Basic Sciences","degree_department":null,"school":null,"contributors":["Mohan, Subburaman"],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011-06-01T07:00:00Z","date_published":"2011-06-01T07:00:00Z","updated_at":"2026-07-24T02:52:08Z","subjects":["Medical Physiology","Osteoporosis, Bone resorption; Bone formation","Novel molecules","Diabetes and Obesity Related Protein (DOR)","Glutaredoxin 5 (Grx5)","Claudin 18 (Cldn-18)"],"languages":["English"],"rights":["This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. The author retains all other copyrights."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://scholarsrepository.llu.edu/etd/40","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor","label":"Contributor","values":["Mohan, Subburaman"]},{"key":"dc:creator","label":"Author","values":["Linares, Gabriel Robert"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_discipline","label":"Discipline","values":["Basic Sciences"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy (PhD)"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Medical Physiology","Osteoporosis, Bone resorption; Bone formation","Novel molecules","Diabetes and Obesity Related Protein (DOR)","Glutaredoxin 5 (Grx5)","Claudin 18 (Cldn-18)"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["English"]},{"key":"dc:rights","label":"Dc Rights","values":["This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. 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We demonstrated that Grx5 protects osteoblasts from oxidative stress induced apoptosis via a molecular pathway that involves regulation of reactive oxygen species production, cardiolipin oxidation, caspase activity, iron-sulfur cluster formation, and manganese superoxide dismutase activity. We found that DOR is an important regulator of osteoblast differentiation. In addition, a single nucleotide polymorphism (SNP) in the promoter of human DOR gene associated with plasma levels of the bone formation marker, osteocalcin, in men. Targeted disruption of the tight junction protein, Cldn-18, in mice led to significant deficits in peak bone mass due to increased bone resorption with no effect on bone formation. Cldn-18 is a novel negative regulator of osteoclast differentiation that interacts with ZO-2 to modulate RANKL signaling in osteoclasts. Collectively, these findings may provide insight into the molecular mechanisms which regulate bone formation and bone resorption, and may be useful in developing therapeutic strategies to prevent low bone mass."]},{"key":"dc:title","label":"Title","values":["Novel Molecules that Regulate Bone Formation and Bone Resorption"]}]}],"canonical_facts":{"dc:contributor":["Mohan, Subburaman"],"dc:creator":["Linares, Gabriel Robert"],"dc:description.abstract":["Osteoporosis is a disease characterized by decreased bone mass and microarchitectural deterioration of bone. Bone loss occurs when the increased bone resorption that occurs with age is not compensated by a corresponding increase in bone formation. Therefore, understanding the mechanisms which regulate bone formation and bone resorption is important for developing diagnostic and treatment strategies for osteoporosis. In my dissertation, we investigated the role of Glutaredoxin 5 (Grx5), Diabetes and Obesity Related protein (DOR), and Claudin 18 (Cldn-18), novel molecules involved in regulating bone formation and bone resorption. We demonstrated that Grx5 protects osteoblasts from oxidative stress induced apoptosis via a molecular pathway that involves regulation of reactive oxygen species production, cardiolipin oxidation, caspase activity, iron-sulfur cluster formation, and manganese superoxide dismutase activity. We found that DOR is an important regulator of osteoblast differentiation. In addition, a single nucleotide polymorphism (SNP) in the promoter of human DOR gene associated with plasma levels of the bone formation marker, osteocalcin, in men. Targeted disruption of the tight junction protein, Cldn-18, in mice led to significant deficits in peak bone mass due to increased bone resorption with no effect on bone formation. Cldn-18 is a novel negative regulator of osteoclast differentiation that interacts with ZO-2 to modulate RANKL signaling in osteoclasts. Collectively, these findings may provide insight into the molecular mechanisms which regulate bone formation and bone resorption, and may be useful in developing therapeutic strategies to prevent low bone mass."],"dc:identifier":["https://scholarsrepository.llu.edu/etd/40"],"dc:language":["English"],"dc:rights":["This title appears here courtesy of the author, who has granted Loma Linda University a limited, non-exclusive right to make this publication available to the public. The author retains all other copyrights."],"dc:subject":["Medical Physiology","Osteoporosis, Bone resorption; Bone formation","Novel molecules","Diabetes and Obesity Related Protein (DOR)","Glutaredoxin 5 (Grx5)","Claudin 18 (Cldn-18)"],"dc:title":["Novel Molecules that Regulate Bone Formation and Bone Resorption"],"thesis:degree_discipline":["Basic Sciences"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy (PhD)"]},"updated_at":"2026-07-24T02:52:08Z"}