Chandan K. Sen

ORCID: 0000-0003-3151-5202
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About
Contact & Profiles
Research Areas
  • Wound Healing and Treatments
  • Diabetic Foot Ulcer Assessment and Management
  • Exercise and Physiological Responses
  • MicroRNA in disease regulation
  • Biochemical Acid Research Studies
  • Muscle metabolism and nutrition
  • Pressure Ulcer Prevention and Management
  • Antioxidant Activity and Oxidative Stress
  • Angiogenesis and VEGF in Cancer
  • Vitamin C and Antioxidants Research
  • Adipose Tissue and Metabolism
  • Bacterial biofilms and quorum sensing
  • Extracellular vesicles in disease
  • Cancer, Hypoxia, and Metabolism
  • Mesenchymal stem cell research
  • Coenzyme Q10 studies and effects
  • Planarian Biology and Electrostimulation
  • Electrospun Nanofibers in Biomedical Applications
  • Mitochondrial Function and Pathology
  • Circular RNAs in diseases
  • RNA Interference and Gene Delivery
  • Tissue Engineering and Regenerative Medicine
  • Burn Injury Management and Outcomes
  • Redox biology and oxidative stress
  • Immune cells in cancer

Indiana University – Purdue University Indianapolis
2018-2025

University of Pittsburgh
2023-2025

McGowan Institute for Regenerative Medicine
2023-2025

Indiana University School of Medicine
2018-2024

Indiana University Health
2018-2024

Center for Neuroscience and Regenerative Medicine
2023-2024

Cook Biotech (United States)
2024

California Institute for Regenerative Medicine
2024

Ann Arbor Center for Independent Living
2024

The Ohio State University
2012-2023

MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the post-transcriptional level by either degradation or translational repression of a target mRNA. Encoded in genome most eukaryotes, miRNAs have been proposed to specifically up 90% human genes through process known as miRNA-guided RNA silencing. For first time, we sought test how myocardial ischaemia-reperfusion (IR) changes miR expression.Following 2 and 7 h IR sham operation, tissue was collected subjected...

10.1093/cvr/cvp015 article EN Cardiovascular Research 2009-01-15

Chronic inflammation is a characteristic feature of diabetic cutaneous wounds. We sought to delineate novel mechanisms involved in the impairment resolution At wound-site, efficient dead cell clearance (efferocytosis) pre-requisite for timely and successful healing.

10.1371/journal.pone.0009539 article EN cc-by PLoS ONE 2010-03-03

Angiogenesis plays a central role in wound healing. Among many known growth factors, vascular endothelial factor (VEGF) is believed to be the most prevalent, efficacious, and long-term signal that stimulate angiogenesis wounds. Whereas direct of copper facilitate has been evident two decades ago, specific targets action remained unclear. This report presents first evidence showing inducible VEGF expression sensitive angiogenic potential may harnessed accelerate dermal contraction closure. At...

10.1152/ajpheart.01015.2001 article EN AJP Heart and Circulatory Physiology 2002-05-01

Previously we have reported in vitro evidence suggesting that H2O2 may support wound healing by inducing VEGF expression human keratinocytes (C. K. Sen et al., 2002, J. Biol. Chem. 277, 33284–33290). Here, test the significance of regulating vivo. Using Hunt–Schilling cylinder approach present first site contains micromolar concentrations H2O2. At site, low supported process, especially p47phox- and MCP-1-deficient mice which endogenous generation is impaired. Higher doses adversely...

10.1016/j.ymthe.2005.07.684 article EN cc-by-nc-nd Molecular Therapy 2005-08-27

Abnormal cardiac ryanodine receptor (RyR2) function is recognized as an important factor in the pathogenesis of heart failure (HF). However, specific molecular causes underlying RyR2 defects HF remain poorly understood. In present study, we used a canine model chronic to test hypothesis that HF-related alterations are caused by posttranslational modification reactive oxygen species generated failing heart. Experimental approaches included imaging cytosolic ([Ca(2+)](c)) and sarcoplasmic...

10.1161/circresaha.108.184457 article EN Circulation Research 2008-11-14

At an injury site, efficient clearance of apoptotic cells by wound macrophages or efferocytosis is a prerequisite for the timely resolution inflammation. Emerging evidence indicates that microRNA-21 (miR-21) may regulate inflammatory response. In this work, we sought to elucidate significance miR-21 in regulation efferocytosis-mediated suppression innate immune response, key process implicated resolving inflammation following injury. An increased expression inducible was noted...

10.4049/jimmunol.1300613 article EN The Journal of Immunology 2014-01-04

Ischemia complicates wound closure. Here, we are unique in presenting a murine ischemic model that is based on bipedicle flap approach. Using this of wounds have sought to elucidate how microRNAs may be implicated limiting re-epithelialization under hypoxia, major component ischemia. Ischemia, evaluated by laser Doppler as well hyperspectral imaging, limited blood flow and lowered tissue oxygen saturation. EPR oximetry demonstrated the had p O 2 <10 mm Hg. Ischemic suffered from...

10.1073/pnas.1001653107 article EN Proceedings of the National Academy of Sciences 2010-03-22

Objective: The objective of this work was to causatively link biofilm properties bacterial infection specific pathogenic mechanisms in wound healing. Background: Staphylococcus aureus is one the four most prevalent species identified chronic wounds. Causatively linking pathology challenging. Thus, isogenic mutant stains S. with varying degree formation ability studied an established preclinical porcine model infection. Methods: Isogenic strains ( ΔrexB > USA300 ΔsarA ) biofilm-forming...

10.1097/sla.0000000000003053 article EN Annals of Surgery 2019-01-03

Inflammation, following injury, induces cellular plasticity as an inherent component of physiological tissue repair. The dominant fate wound macrophages is unclear and debated. Here we show that two-thirds all granulation fibroblasts, otherwise known to be mesenchymal origin, are derived from myeloid cells which likely macrophages. Conversion fibroblast-like impaired in diabetic wounds. In cross-talk between keratinocytes cells, miR-21 packaged extracellular vesicles (EV) required for cell...

10.1038/s41467-018-03208-w article EN cc-by Nature Communications 2018-02-27
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