期刊文献+

Systems biology approach to developing S^2RM-based “systems therapeutics” and naturally induced pluripotent stem cells

Systems biology approach to developing S^2RM-based “systems therapeutics” and naturally induced pluripotent stem cells
下载PDF
导出
摘要 The degree to, and the mechanisms through, which stem cells are able to build, maintain, and heal the body have only recently begun to be understood. Much of the stem cell's power resides in the release of a multitude of molecules, called stem cell released molecules(SRM). A fundamentally new type of therapeutic, namely "systems therapeutic", can be realized by reverse engineering the mechanisms of the SRM processes. Recent data demonstrates that the composition of the SRM is different for each type of stem cell, as well as for different states of each cell type. Although systemsbiology has been successfully used to analyze multiple pathways, the approach is often used to develop a small molecule interacting at only one pathway in the system. A new model is emerging in biology where systems biology is used to develop a new technology acting at multiple pathways called "systems therapeutics". A natural set of healing pathways in the human that uses SRM is instructive and of practical use in developing systems therapeutics. Endogenous SRM processes in the human body use a combination of SRM from two or more stem cell types, designated as S2 RM, doing so under various state dependent conditions for each cell type. Here we describe our approach in using statedependent SRM from two or more stem cell types, S2 RM technology, to develop a new class of therapeutics called "systems therapeutics." Given the ubiquitous and powerful nature of innate S2RM-based healing in the human body, this "systems therapeutic" approach using S2 RM technology will be important for the development of anti-cancer therapeutics, antimicrobials, wound care products and procedures, and a number of other therapeutics for many indications. The degree to, and the mechanisms through, whichstem cells are able to build, maintain, and heal the bodyhave only recently begun to be understood. Much of thestem cell's power resides in the release of a multitudeof molecules, called stem cell released molecules (SRM).A fundamentally new type of therapeutic, namely"systems therapeutic", can be realized by reverseengineering the mechanisms of the SRM processes.Recent data demonstrates that the composition of theSRM is different for each type of stem cell, as well asfor different states of each cell type. Although systemsbiology has been successfully used to analyze multiplepathways, the approach is often used to develop a smallmolecule interacting at only one pathway in the system.A new model is emerging in biology where systemsbiology is used to develop a new technology actingat multiple pathways called "systems therapeutics". Anatural set of healing pathways in the human that usesSRM is instructive and of practical use in developingsystems therapeutics. Endogenous SRM processes inthe human body use a combination of SRM from twoor more stem cell types, designated as S2RM, doing sounder various state dependent conditions for each celltype. Here we describe our approach in using statedependentSRM from two or more stem cell types,S2RM technology, to develop a new class of therapeuticscalled "systems therapeutics." Given the ubiquitous andpowerful nature of innate S2RM-based healing in thehuman body, this "systems therapeutic" approach usingS2RM technology will be important for the developmentof anti-cancer therapeutics, antimicrobials, woundcare products and procedures, and a number of othertherapeutics for many indications.
机构地区 SRM Living Foundry
出处 《World Journal of Stem Cells》 SCIE CAS 2015年第4期745-756,共12页 世界干细胞杂志(英文版)(电子版)
关键词 Stem cell PARACRINE Growth factors PLURIPOTENCY WOUND HEALING Cancer Stem cell Paracrine Growth factors Pluripotency Wound healing Cancer
  • 相关文献

参考文献93

  • 1Cauffman G, De Rycke M, Sermon K, Liebaers I, Van de VeldeH. Markers that define stemness in ESC are unable to identify thetotipotent cells in human preimplantation embryos. Hum Reprod2009; 24: 63-70 [PMID: 18824471 DOI: 10.1093/humrep/den351].
  • 2Macotela Y, Emanuelli B, Mori MA, Gesta S, Schulz TJ, TsengYH, Kahn CR. Intrinsic differences in adipocyte precursor cellsfrom different white fat depots. Diabetes 2012; 61: 1691-1699[PMID: 22596050 DOI: 10.2337/db11-1753].
  • 3Ong WK, Tan CS, Chan KL, Goesantoso GG, Chan XH, ChanE, Yin J, Yeo CR, Khoo CM, So JB, Shabbir A, Toh SA, Han W,Sugii S. Identification of specific cell-surface markers of adiposederivedstem cells from subcutaneous and visceral fat depots. StemCell Reports 2014; 2: 171-179 [PMID: 24527391 DOI: 10.1016/j.stemcr.2014.01.002].
  • 4Sze SK, de Kleijn DP, Lai RC, Khia Way Tan E, Zhao H, Yeo KS,Low TY, Lian Q, Lee CN, Mitchell W, El Oakley RM, Lim SK.Elucidating the secretion proteome of human embryonic stemcell-derived mesenchymal stem cells. Mol Cell Proteomics 2007;6: 1680-1689 [PMID: 17565974 DOI: 10.1074/mcp.M600393-MCP200].
  • 5Ribeiro CA, Fraga JS, Gr-os M, Neves NM, Reis RL, Gimble JM,Sousa N, Salgado AJ. The secretome of stem cells isolated from theadipose tissue and Wharton jelly acts differently on central nervoussystem derived cell populations. Stem Cell Res Ther 2012; 3: 18[PMID: 22551705 DOI: 10.1186/scrt109].
  • 6Berardis S, Lombard C, Evraerts J, El Taghdouini A, Rosseels V,Sancho-Bru P, Lozano JJ, van Grunsven L, Sokal E, Najimi M.Gene expression profiling and secretome analysis differentiateadult-derived human liver stem/progenitor cells and human hepaticstellate cells. PLoS One 2014; 9: e86137 [PMID: 24516514 DOI:10.1371/journal.pone.0086137].
  • 7Kato T, Okumi M, Tanemura M, Yazawa K, Kakuta Y, YamanakaK, Tsutahara K, Doki Y, Mori M, Takahara S, Nonomura N.Adipose tissue-derived stem cells suppress acute cellular rejectionby TSG-6 and CD44 interaction in rat kidney transplantation.Transplantation 2014; 98: 277-284 [PMID: 24983309 DOI:10.1097/TP.0000000000000230].
  • 8Crisostomo PR, Wang M, Wairiuko GM, Morrell ED, TerrellAM, Seshadri P, Nam UH, Meldrum DR. High passage numberof stem cells adversely affects stem cell activation and myocardialprotection. Shock 2006; 26: 575-580 [PMID: 17117132 DOI:10.1097/01.shk.0000235087.45798.93].
  • 9Deschene ER, Myung P, Rompolas P, Zito G, Sun TY, Taketo MM,Saotome I, Greco V. β-Catenin activation regulates tissue growthnon-cell autonomously in the hair stem cell niche. Science 2014;343: 1353-1356 [PMID: 24653033 DOI: 10.1126/science.1248373].
  • 10Park CW, Kim KS, Bae S, Son HK, Myung PK, Hong HJ, Kim H.Cytokine secretion profiling of human mesenchymal stem cells byantibody array. Int J Stem Cells 2009; 2: 59-68 [PMID: 24855521DOI: 10.15283/ijsc.2009.2.1.59].

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部