Photo of Herb B. (Hui Bin) Sun

Herb B. (Hui Bin) Sun

  • ADJUNCT ASSISTANT PROFESSOR Orthopaedics
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Research

Research

Specific Clinical/Research Interest:
Gene regulation and signal transduction of joint tissue homeostasis; mechanotransduction pathway and its potential use for disease prevention and treatment; effects of chemo-factors and mechano-factors on MSC renewal, commitment, and differentiation; role of MSCs in wound healing and tissue engineering
Current Students: Melissa Ramcharan, Daniel Leong, Jonathan Lee, Edward Maharam
Postdoctoral Fellows: Zhengzhe Li, MD, Ph.D
Summary of Research Studies:
The focus of our integrated systems-based research is to elucidate the molecular mechanism of signal transduction in skeletal tissue. The goal of the research is to provide molecular and signaling base for preventing and for therapeutic treatment of skeletal breakdown diseases such as arthritis, osteoporosis, tendonopathy. Three specific interests are: Role of mechanical stimuli in preventing cartilage/tendon breakdown: Our research project has provided strong evidence that gentle mechanical load exerts a role in preventing skeleton tissue degeneration; and that CITED2 (CBP/p300-Interacting Transactivator with ED-rich tail 2), a cytokine and stress inducible gene that I cloned previously, plays a critical role in tissue-breakdown. Based on computational analysis for biological experiment data, the current project is focusing on CITED2 mediated novel signaling pathway in modulation of matrix homeostasis. Mechanism of load-induced bone formation: Mechanical loading is a potent stimulator of bone growth. Using a novel 3-dimensional osteoblasts culture-piezoelectric mechanical loader, our laboratory is now able to induce osteo-mineralization in vitro. We are currently using this novel in vitro model to identify key signaling pathways and critical biological and mechanical environment factors for osteo-mineralization and bone formation. In our in vivo study, we have recently demonstrated that sinusoidal loads to an elbow joint stimulate bone formation in cortical bone without bone deformation. Using pathway-specific cDNA-array, trans-signal protein-array and other molecular technologies, this in vivo study is focusing on identifying the critical signaling pathway in bone formation induced by neighboring joint deformation. Identification of cellular signaling pathway by genome-wide transcription analysis: We have developed a novel approach in integrating the experimental data and genomic DNA sequences. This computational and biochemical tool demonstrated in the model of chondrocyte cellular response to interleukine-1, can be used for any biological process including molecular and cellular mechanism of mechanotransduction of joint, tendon, and bone. Using biotin-avidin affinity binding and protein fingerprints technologies, the current project is aiming at cloning novel transactivators that binds to the identified DNA binding motifs. Accomplishment of this project will result in not only cloning new signal molecules in tissue-breakdown but also proving our experiment-based genome-wide cloning strategy.

Publications

Sun HB, Zhu YX, Yin T, Sledge G, Yang YC. MRG1, the production of a melanocyte-specific gene related gene, is a cytokine-inducible transcription factor with transformation activity. Proc. Natl. Acad. Sci. USA 1998; 95: 13555-13560.

Sun HB, Yokota H. Messenger RNA levels of matrix metalloproteinases, tissue inhibitors of metalloproteinases, and transcription factors in rheumatic synovial cells under mechanical stimuli. Bone 2001; 28: 303-309.

Sun HB, Yokota H. Altered mRNA levels of matrix metalloproteinase 13 in MH7A synovial cells by mechanical loading. Bone 2001; 28: 399-403.

Sun HB, Malacinski GM, Yokota H. Promoter competition assay for analyzing gene regulation in joint tissue engineering. Frontiers in Bioscience 2002; 7: 169-174.

Sun HB, Yokota H. Reduction of cytokine-induced expression and activities of MMP-1 and MMP-13 by mechanical strain in MH7A rheumatoid synovial cells. Matrix Biol 2002; 21: 263-270.

Sun HB, Liu Y, Qian L, Yokota H. Model-based analysis of matrix metalloproteinases expression under mechanical shear. Ann. Biomed. Eng 2003; 31: 171-180.

Sun HB, Nalim R, Yokota H. Expression and activities of matrix metalloproteinases under oscillatory shear in IL-1 stimulated rheumatic synovial cells. Connective Tissue Res 2003; 44: 42-49.

Yokota H, Goldring MB, Sun HB. CITED2 mediated regulation of MMP-1 and MMP-13 in human chondrocytes under flow shear. J. Biol. Chem 2003; 278: 47275-47280.

Industry Relationships

Physicians and scientists on the faculty of the Icahn School of Medicine at Mount Sinai often interact with pharmaceutical, device and biotechnology companies to improve patient care, develop new therapies and achieve scientific breakthroughs. In order to promote an ethical and transparent environment for conducting research, providing clinical care and teaching, Mount Sinai requires that salaried faculty inform the School of their relationships with such companies.

Dr.Sun is not currently required to report Industry relationships.

Mount Sinai's faculty policies relating to faculty collaboration with industry are posted on our website at http://icahn.mssm.edu/about-us/services-and-resources/faculty-resources/handbooks-and-policies/faculty-handbook. Patients may wish to ask their physician about the activities they perform for companies.

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