WSWorawalan Samruan

Worawalan Samruan

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Worawalan Samruan has a total of 7 co-authors. Here are the top co-authors by number of shared publications:

  • Irene Aksoy

    Univ Lyon, Université Lyon 1, INSERM, Stem Cell and Brain Research Institute U1208, 69500 Lyon, France

    2 shared publications
  • Jittanun Srisutush

    Embryo Technology and Stem Cell Research Center, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

    2 shared publications
  • Pierre Savatier

    Univ Lyon, Université Lyon 1, INSERM, Stem Cell and Brain Research Institute U1208, 69500 Lyon, France

    2 shared publications
  • Preeyanan Anwised

    Embryo Technology and Stem Cell Research Center, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

    2 shared publications
  • Rangsun Parnpai

    Embryo Technology and Stem Cell Research Center, School of Biotechnology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

    2 shared publications
  • Ratree Moorawong

    Embryo Technology and Stem Cell Research Center, School of Biotechnology, Institute of Agricultural Technology, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

    2 shared publications

Latest Publications

  • Open Access

    Driving Naive State Induction Using Human Wharton Jelly-Mesenchymal Stem Cell-Derived Conditioned Medium in Rhesus Monkey Embryonic Stem Cells

    by Preeyanan Anwised, Ratree Moorawong, Worawalan Samruan, Jittanun Srisutush, Sirilak Somredngan, Irene Aksoy, Pierre Savatier, Rangsun Parnpai

    The conversion of primed pluripotent stem cells to a naive-like state has emerged as a critical strategy for enhancing developmental potential and broadening applications in regenerative medicine. Conditioned media (CM)-based approaches provide a supportive microenvironment enriched with secreted factors that may facilitate this state transition without extensive genetic or chemical manipulation. In this study, we investigated the potential of human Wharton’s Jelly-derived mesenchymal stem cell-conditioned media (hWJ-MSCs-CM) and mouse embryonic fibroblasts CM (MEFs-CM) to support the conversion of primed rhesus monkey embryonic stem cells (rhESCs) into a naive-like state. The rhESCs were cultured under feeder-free and feeder conditions using both hWJ-MSCs-CM and MEFs-CM, exhibiting distinct morphological changes during conversion. Immunofluorescence analysis demonstrated the expression of pluripotency and naive markers under both conditions. Gene expression analysis further confirmed the upregulation of naive-specific genes and downregulation of primed markers, with statistically significant differences between groups. Additionally, epigenetic reprogramming was assessed, revealing differential effects of the CM sources on the reversion to a naive state. These findings highlight the potential of hWJ-MSCs-CM as a supportive system for naive-like state induction in primate ESCs.


  • Open Access

    Driving Naïve State Induction Using Human Wharton Jelly-Mesenchymal Stem Cell-Derived Conditioned Medium in Rhesus Monkey Embryonic Stem Cells

    by Preeyanan Anwised, Ratree Moorawong, Worawalan Samruan, Jittanun Srisutush, Sirilak Somredngan, Irene Aksoy, Pierre Savatier, Rangsun Parnpai

    This study aimed to examine the potential of human Wharton’s Jelly-derived mes-enchymal stem cells (hWJ-MSCs) in supporting the conversion of the primed state of rhesus monkey embryonic stem cells (rhESCs) to a naïve-like state. The rhESCs were cultured under feeder-free and feeder conditions using hWJ-MSC-conditioned media (hWJ-MSCs-CM) and mouse embryonic fibroblasts CM (MEFs-CM) exhibited distinct morphological changes during conversion. Immunofluorescence analysis demonstrated the expression of pluripotency and naïve markers under both condi-tions. Gene expression analysis further confirmed the upregulation of naïve-specific genes and downregulation of primed markers, with statistically significant differ-ences between groups. Additionally, epigenetic reprogramming was assessed, re-vealing differential effects of the CM sources on the reversion to a naïve state. These findings highlight the potential of hWJ-MSCs-CM as a supportive system for na-ïve-state induction in primate ESCs.