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Dr. Sam J. Mathew
Professor
  • PhD, University of Cologne, Germany (2006)
  • Postdoctoral Research at University of Utah, USA
  • Associate Professor at RCB since 2019
sjmathew[at]rcb[dot]res[dot]in

Research Theme: Mammalian development, stem cells, regeneration and disease

Stem cells are specialized cells crucial for embryonic development, adult tissue maintenance and repair, and play vital roles in diseases such as muscular dystrophy and cancer. Using mammalian genetic models, our lab is interested in deciphering the mechanisms underlying four important events and processes that occur during the life span of mammals: 

1. embryonic development, 

2. stem cell-mediated regeneration, 

3. tissue homeostasis, and

4. diseases. 

First, during development, embryonic stem cells undergo a predetermined program of differentiation, controlled by autocrine and paracrine signals. We aim to unravel the mechanisms underlying muscle differentiation, identifying the genes and pathways involved. Second, regeneration of the adult skeletal muscle is primarily carried out by the muscle-resident stem cells known as satellite cells. 

We are studying how the satellite cells remain dormant normally, are activated upon injury and various signals control their function. Third, we are interested in understanding the maintenance of the skeletal muscle, a contractile, highly metabolically active tissue, contributes to overall body homeostasis. Among the signals that regulate muscle homeostasis, we identified one to be mechanical, called mechanotransduction. 

Fourth, stem cell function is associated with numerous diseases and therapies, where we have multiple interests. Cancers such as rhabdomyosarcoma occur due to uncontrolled proliferation of muscle stem cells, where we are identifying the pathways and genes affected, for use as therapeutic targets.

Genetic diseases such as Duchenne Muscular Dystrophy, Spondylocarpotarsal Synostosis, Limb-Girdle Muscular Dystrophy and several more are caused by mutations in specific genes crucial for muscle function. 

We are developing cellular and animal models to understand such diseases, characterize the disease pathology, identify dysregulated molecular pathways and develop therapies, such as using induced pluripotent stem cells (iPSCs).

We are also studying how skeletal muscle dysfunction contributes to neurodegenerative diseases such as Parkinson’s disease and lifestyle diseases such as type 2 diabetes.

  • Wellcome-DBT Intermediate Fellow

Selected Publications

All Publications

  1. Kumar, P., Zehra, A., Saini, M., and Mathew, S. J. (2023). Zeb1 and Tle3 are trans-factors that differentially regulate the expression of myosin heavy chain-embryonic and skeletal muscle differentiation. FASEB Journal 37(8):e23074. doi: 10.1096/fj.202201698RR
  2. Agarwal M, Bharadwaj A, Mathew S.L. (2022) TLE4 regulates muscle stem cell quiescence and skeletal muscle differentiation Journal of Cell Science, 135:4
  3. Pradhan AK, G. Kandasamy, U. Chatterjee, A. Bharadwaj, S.J. Mathew, R.J. Dohmen, and Palanimurugan R. (2021) Ribosome-associated quality control mediates degradation of the premature translation termination product Orf1p of ODC antizyme mRNA. FEBS Letters 595: 2015-2033. doi: 10.1002/1873-3468.14147
  4. Agarwal M, A. Sharma, P. Kumar, A. Kumar, and S.J. Mathew. 2020. The people behind the papers. Development 147(7). pii: dev190025. doi: 10.1242/dev.190025.
  5. Agarwal M, A. Sharma, P. Kumar, A. Kumar, A. Bharadwaj, M. Saini, G. Kardon, and S.J. Mathew. (2020) Myosin heavy chain-embryonic regulates skeletal muscle differentiation during mammalian development. Development 147(7). pii: dev184507. doi: 10.1242/dev.184507.
  6. Das S, P Kumar, A Verma, TK Maiti, and Mathew SJ (2019) Myosin heavy chain mutations that cause Freeman-Sheldon syndrome lead to muscle structural and functional defects in Drosophila Developmental Biology | 449(2): 90-98.
  7. M Saini , A Verma, SJ Mathew. (2018) SPRY2 is a novel MET interactor that regulates metastatic potential and differentiation in rhabdomyosarcoma. Cell Death and Disease 9:237
  8. Agarwal M, Kumar P, Mathew SJ (2015)  The Groucho/Transducin-like enhancer of split protein family in animal development. IUBMB Life 67:472.
  9. Keefe AC, Lawson JA, Flygare SD, Fox ZD, Colasanto MP, Mathew SJ, Yandell M, Kardon G. (2015) Muscle stem cells contribute to myofibres in sedentary adult mice. Nature Communications 14;6:7087 (Recommended by Faculty of 1000).
  10. Mathew SJ, Rembold M, Leptin M. (2011) A role for Traf4 in polarizing adherens junctions as a prerequisite for efficient cell shape changes. Molecular and Cellular Biology 24:4978.
  11. Murphy MM, Lawson JA, Mathew SJ, Hutcheson DA, Kardon G. (2011) Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration. Development 138:3625-3637. (Featured article, Recommended by Faculty of 1000)
  12. Mathew SJ. (2011) InACTIVatINg cancer cachexia. Dis Model Mech 4:283.
  13. Mathew SJ, Hansen JM, Merrell AJ, Murphy MM, Lawson JA, Hutcheson DA, Hansen MS, Angus-Hill M, Kardon G. (2011) Connective tissue fibroblasts and Tcf4 regulate myogenesis. Development 138:371-384.
  14. Mathew SJ, Haubert D, Kronke M, Leptin M. (2009) Looking beyond death: a morphogenetic role for the TNF signalling pathway. J Cell Sci 122:1939.
  15. Mathew SJ, Kerridge S, Leptin M. (2009) A small genomic region containing several loci required for gastrulation in Drosophila. PLoS One 4:e7437
Dr. Sam J. Mathew
Professor

Regional Centre for Biotechnology
NCR Biotech Science Cluster
3rd Milestone, Faridabad-Gurgaon Expressway
P.O. Box No. 3, Faridabad - 121 001
Haryana (NCR Delhi), India

no text sjmathew[at]rcb[dot]res[dot]in
no text +91 129-2848822

Dr. Sam J. Mathew