Risbud, Makarand V.
Makarand V. Risbud, PhD
Suite 501, Curtis Bldg.
Philadelphia, PA 19107
MSc, Biochemistry, University of Pune - 1997
M.Tech., Indian Institute of Technology (IIT): Bombay - 1999
PhD, National Center for Cell Science, India - 2001
Post Doc Fellowship, Harvard University, Boston, 2001-2002
James J. Maguire Jr. Professor of Spine Research, Department of Orthopaedic Surgery
Co-Director, Cell Biology & Regenerative Medicine Graduate Program
Expertise & Research Interests
Major research focus of my lab is to study the mechanisms by which nucleus pulposus cells of the intervertebral disc adapt to avascular (hypoxic) and osmotically compromising environment. In this regard, we are studying role of transciption factors HIFs and TonEBP and signaling events that control their function. Another major research interest is to device tissue-enginering based strategies for intervertebral disc regeneration. We are testing hypothesis that adult mesenchymal stem cells (MSC) transplanted into the disc will assume nucleus pulposus-like phenotype and achieve functional restoration of degenerate disc. Our recent work shows that MSC differentiate into nucleus pulposus-like cells when cultured under conditions similar to that exist in the disc in vivo. A whole disc organ culture is also under investigation to understand aspects of disc cell function in an ex vivo setting.
Cell-Scaffold intereactions at molecular level and chitosan based scaffolds
My reaserch has a strong translational component. Regeneration of degenerate intervertberal disc using adult-mesenchymal stem cells could be a clinical therapy in future and is of immense interest to many biotech and health science companies.
Intervertebral Disc; Mesenchymal Stem Cells; Nucleus Pulposus Cells; Hypoxia; HIF-1, hypertonicity, TonEBP, Cell signaling; Tissue Engineering, Scaffolds
English, Hindi, Marathi
Most Recent Peer-Reviewed Publications
- Bicarbonate Recycling by HIF-1–Dependent Carbonic Anhydrase Isoforms 9 and 12 Is Critical in Maintaining Intracellular pH and Viability of Nucleus Pulposus Cells
- Lack of evidence for involvement of TonEBP and hyperosmotic stimulus in induction of autophagy in the nucleus pulposus
- PHD3 is a transcriptional coactivator of HIF-1a in nucleus pulposus cells independent of the PKM2-JMJD5 axis
- New horizons in spine research: Intervertebral disc repair and regeneration
- TNF-α promotes nuclear enrichment of the transcription factor TonEBP/NFAT5 to selectively control inflammatory but not osmoregulatory responses in nucleus pulposus cells
- RNA sequencing reveals a role of TonEBP transcription factor in regulation of pro-inflammatory genes in response to hyperosmolarity in healthy nucleus pulposus cells a homeostatic response?
- Hypoxia promotes noncanonical autophagy in nucleus pulposus cells independent of MTOR and HIF1A signaling
- New Horizons in Spine Research: Disc biology, spine biomechanics and pathomechanisms of back pain
- Molecular mechanisms of biological aging in intervertebral discs
- N-cadherin is key to expression of the nucleus pulposus cell phenotype under selective substrate culture conditions
- Class i and IIa HDACs Mediate HIF-1α Stability Through PHD2-Dependent Mechanism, while HDAC6, a Class IIb Member, Promotes HIF-1α Transcriptional Activity in Nucleus Pulposus Cells of the Intervertebral Disc
- Syndecan-4 in intervertebral disc and cartilage: Saint or synner?
- The mRNA-binding protein HuR promotes hypoxia-induced chemoresistance through posttranscriptional regulation of the proto-oncogene PIM1 in pancreatic cancer cells
- Circadian factors BMAL1 and RORα control HIF-1α transcriptional activity in nucleus pulposus cells: Implications in maintenance of intervertebral disc health
- TGFβ regulates Galectin-3 expression through canonical Smad3 signaling pathway in nucleus pulposus cells: Implications in intervertebral disc degeneration
- Matrix vesicles: Are they anchored exosomes?
- Understanding nucleus pulposus cell phenotype: A prerequisite for stem cell based therapies to treat intervertebral disc degeneration
- Prolyl-4-hydroxylase domain protein 2 controls NF-κB/p65 transactivation and enhances the catabolic effects of inflammatory cytokines on cells of the nucleus pulposus
- Discovery of the drivers of inflammation induced chronic low back pain: From bacteria to diabetes
- Disc in flames: Roles of TNF-α and IL-1β in intervertebral disc degeneration