Human Embryonic Stem Cells hESC Therapy

Regen Center Glossary

Human embryonic stem cell line or hESC are also referred to as simply Embryonic stem cells. ES cells pertains to a pluripotent lineage of cells that are typically derived from a human embryo (after zygote) at its earliest stage.

 Embyronic Stem Cell Biology

Embryonic cells of the morular are totipotent. ES cells are considered very powerful in regenerative medicine since they can undergo cell division even without differentiation, which could go for extended periods,[3] and eventually develop into the cells composing the three germ layers.

There are 3 types of pluripotent cells that occur:

    • Embryonic Stem (ES) Cells. ES Cells can be isolated in the lab from the ICM or inner cell mass of a blastocyst.Embryos for ES cell treatments are usually produced naturally during IVF therapy. In most countries around the world including Thailand, harvesting ES cell lines from human donated blastocysts forbidden because the belief that it destroys a human embryo
    • Embryonic Carcinoma (EC) Cells are is the 3rd type of pluripotent cell that can be isolated from teratocarcinomas (occasional tumors in the gonads of a fetus)
    • Embryonic Germ (EG) Stemcells can isolated from the precursor to human gonads but requires aborted fetuses.


All 3 of the previous ES cells typically require isolation from fetal or embryonic tissue. Some ES lines such as induced pluripotent cells however can now be can be cultured in our labs using special growth medium but are still very difficult to control during mesoderm production and the differentiation process.[2]


The Regeneration center of Thailand does not use Embryonic stemcell lines in any of its treatments. Our cell therapies use allogeneic or autologous Adult stem cells only.

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Published Clinical Citations

  • [1] ^ Yang, Heung-Mo, Sung-Hwan Moon, Young-Sil Choi, Soon-Jung Park, Yong-Soo Lee, Hyun-Joo Lee, Sung-Joo Kim, and Hyung-Min Chung. 2013. Therapeutic efficacy of human embryonic stem cell-derived endothelial cells in humanized mouse models harboring a human immune system. Arteriosclerosis, thrombosis, and vascular biology, no. 12 (October 3). doi:10.1161/ATVBAHA.113.302462. https://www.ncbi.nlm.nih.gov/pubmed/24092748

  • [2] ^ Soteriou, Despina, Banu Iskender, Adam Byron, Jonathan D Humphries, Simon Borg-Bartolo, Marie-Claire Haddock, Melissa A Baxter, David Knight, Martin J Humphries, and Susan J Kimber. 2013. Comparative proteomic analysis of supportive and unsupportive extracellular matrix substrates for human embryonic stem cell maintenance. The Journal of biological chemistry, no. 26 (May 8). doi:10.1074/jbc.M113.463372. https://www.ncbi.nlm.nih.gov/pubmed/23658023

  • [3] ^ Hung, Sandy S C, Raymond C B Wong, Alexei A Sharov, Yuhki Nakatake, Hong Yu, and Minoru S H Ko. 2013. Repression of global protein synthesis by Eif1a-like genes that are expressed specifically in the two-cell embryos and the transient Zscan4-positive state of embryonic stem cells. DNA research : an international journal for rapid publication of reports on genes and genomes, no. 4 (May 5). doi:10.1093/dnares/dst018. https://www.ncbi.nlm.nih.gov/pubmed/23649898