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Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow.

Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Research Abstract Details 

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  • Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Abstract Text:

    ming-song tsaiMing-Song Tsai,shiaw-min hwangShiaw-Min Hwang,kuang-den chenKuang-Den Chen,yun-shien leeYun-Shien Lee,li-wen hsuLi-Wen Hsu,yu-jen changYu-Jen Chang,chao-nin wangChao-Nin Wang,hsiu-huei pengHsiu-Huei Peng,yao-lung changYao-Lung Chang,an-shine chaoAn-Shine Chao,shuenn-dyh changShuenn-Dyh Chang,kuan-der leeKuan-Der Lee,tzu-hao wangTzu-Hao Wang,hsin-shih wangHsin-Shih Wang,yung-kuei soongYung-Kuei Soong,ming-song tsaiMing-Song Tsai,shiaw-min hwangShiaw-Min Hwang,kuang-den chenKuang-Den Chen,yun-shien leeYun-Shien Lee,li-wen hsuLi-Wen Hsu,yu-jen changYu-Jen Chang,chao-nin wangChao-Nin Wang,hsiu-huei pengHsiu-Huei Peng,yao-lung changYao-Lung Chang,an-shine chaoAn-Shine Chao,shuenn-dyh changShuenn-Dyh Chang,kuan-der leeKuan-Der Lee,tzu-hao wangTzu-Hao Wang,hsin-shih wangHsin-Shih Wang,yung-kuei soongYung-Kuei Soong,ming-song tsaiMing-Song Tsai,shiaw-min hwangShiaw-Min Hwang,kuang-den chenKuang-Den Chen,yun-shien leeYun-Shien Lee,li-wen hsuLi-Wen Hsu,yu-jen changYu-Jen Chang,chao-nin wangChao-Nin Wang,hsiu-huei pengHsiu-Huei Peng,yao-lung changYao-Lung Chang,an-shine chaoAn-Shine Chao,shuenn-dyh changShuenn-Dyh Chang,kuan-der leeKuan-Der Lee,tzu-hao wangTzu-Hao Wang,hsin-shih wangHsin-Shih Wang,yung-kuei soongYung-Kuei Soong,

    Using high-density oligonucleotide microarrays and functional network analyses, we examined whether MSCs derived from four different origins exhibited unique gene expression profiles individually and then compared the gene expression profiles of all MSCs with those of fetal organs. Our results indicated that within each group of MSCs from the same origin, the variability of the gene expression levels was smaller than that between groups of different origins. Functional genomic studies revealed the specific roles of MSCs from different origins. Our results suggest that amniotic fluid MSCs may initiate interactions with the uterus by upregulating oxytocin and thrombin receptors. Amniotic membrane MSCs may play a role in maintaining homeostasis of fluid and electrolytes by regulating the networks of endothelin, neprilysin, bradykinin receptors, and atrial natriuretic peptide. Cord blood MSCs may be involved in innate immune systems as the neonatal defense system against the earliest encountered pathogens. Adult bone marrow MSCs may be an important source not only of all blood lineages but also of bone formation. However, in spite of the different gene expression profiles seen in MSCs derived from different origins, a set of core gene expression profiles was preserved in these four kinds of MSCs. The core signature transcriptomes of all MSCs, when contrasted against those of fetal organs, included genes involved in the regulation of extracellular matrix and adhesion, transforming growth factor-beta receptor signaling, and the Wnt signaling pathways. Disclosure of potential conflicts of interest is found at the end of this article.

    Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Publishing Authors By Initials

    ms tsaiMS Tsai,sm hwangSM Hwang,kd chenKD Chen,ys leeYS Lee,lw hsuLW Hsu,yj changYJ Chang,cn wangCN Wang,hh pengHH Peng,yl changYL Chang,as chaoAS Chao,sd changSD Chang,kd leeKD Lee,th wangTH Wang,hs wangHS Wang,yk soongYK Soong,ms tsaiMS Tsai,sm hwangSM Hwang,kd chenKD Chen,ys leeYS Lee,lw hsuLW Hsu,yj changYJ Chang,cn wangCN Wang,hh pengHH Peng,yl changYL Chang,as chaoAS Chao,sd changSD Chang,kd leeKD Lee,th wangTH Wang,hs wangHS Wang,yk soongYK Soong,ms tsaiMS Tsai,sm hwangSM Hwang,kd chenKD Chen,ys leeYS Lee,lw hsuLW Hsu,yj changYJ Chang,cn wangCN Wang,hh pengHH Peng,yl changYL Chang,as chaoAS Chao,sd changSD Chang,kd leeKD Lee,th wangTH Wang,hs wangHS Wang,yk soongYK Soong,

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    PUBMED ID PMID:

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    Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Stem cells (Dayton, Ohio)

    VOLUME: 25

    Page Numbers: 2511-23

    Journal Abbreviation: Stem Cells

    ISSN: 1549-4918

    DAY: 7

    MONTH: 06

    YEAR: 2007

    Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9304532

    Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Keywords Mesh Terms:

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    Chemical & Substance for Abstract: Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow. Information

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    Grant and Affiliation Information for Functional network analysis of the transcriptomes of mesenchymal stem cells derived from amniotic fluid, amniotic membrane, cord blood, and bone marrow.

    AFFILIATION: Prenatal Diagnosis Center, Cathay General Hospital, Taipei, Taiwan.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Stem Cells

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