Regulation and guidance of cell behavior for tissue regeneration via the siRNA mechanism

被引:43
作者
Cheema, Sangeeta K.
Chen, Ellen
Shea, Lonnie D.
Mathur, Anshu B.
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Plast Surg, Houston, TX 77230 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Expt Therapeut, Houston, TX 77230 USA
[3] Northwestern Univ, Dept Biol & Chem Engn, Evanston, IL USA
关键词
D O I
10.1111/j.1524-475X.2007.00228.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNA intereference and short-interfering RNA (siRNA) have been proven to be effective at decreasing the expression of target genes and provide a valuable tool for promoting and directing the growth of functional tissues for repair and reconstructive tissue engineering applications. siRNA is a gene-silencing mechanism that involves double-stranded RNA-mediated sequence-specific mRNA degradation and is a powerful mechanism for controlling cell behavior. The use of siRNA to reduce the expression of a target gene can induce the expression of one or more tissue-inductive factors, direct the differentiation of stem or progenitor cells, or remove a factor that inhibits regeneration, which can be useful in fundamental studies of tissue formation or in applications to promote in vivo regeneration. The potential of siRNA is illustrated through specific examples within the fields of angiogenesis, bone and nerve regeneration, and wound healing. In addition, challenges to deliver siRNA effectively for tissue engineering applications are addressed. siRNA represents a powerful tool to investigate and/or promote tissue formation, and numerous opportunities exist for identifying targets that promote regeneration of tissue and developing effective delivery systems.
引用
收藏
页码:286 / 295
页数:10
相关论文
共 59 条
  • [11] Evidence for a role of hyaluronan in the spacing of fibrils within collagen bundles in rabbit synovium
    Coleman, PJ
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 2002, 1571 (03): : 173 - 182
  • [12] Structural variations and stabilising modifications of synthetic siRNAs in mammalian cells
    Czauderna, F
    Fechtner, M
    Dames, S
    Aygün, H
    Klippel, A
    Pronk, GJ
    Giese, K
    Kaufmann, J
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (11) : 2705 - 2716
  • [13] Design of modular non-viral gene therapy vectors
    De Laporte, L
    Rea, JC
    Shea, LD
    [J]. BIOMATERIALS, 2006, 27 (07) : 947 - 954
  • [14] Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation
    Ducy, P
    Zhang, R
    Geoffroy, V
    Ridall, AL
    Karsenty, G
    [J]. CELL, 1997, 89 (05) : 747 - 754
  • [15] The vesiculo-vacuolar organelle (VVO): A new endothelial cell permeability organelle
    Dvorak, AM
    Feng, D
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2001, 49 (04) : 419 - 431
  • [16] Induction of hypervascularity without leakage or inflammation in transgenic mice overexpressing hypoxia-inducible factor-1α
    Elson, DA
    Thurston, G
    Huang, LE
    Ginzinger, DG
    McDonald, DM
    Johnson, RS
    Arbeit, JM
    [J]. GENES & DEVELOPMENT, 2001, 15 (19) : 2520 - 2532
  • [17] Scar-free healing: from embryonic mechanisms to adult therapeutic intervention
    Ferguson, MWJ
    O'Kane, S
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 2004, 359 (1445) : 839 - 850
  • [18] Repulsive factors and axon regeneration in the CNS
    Fournier, AE
    Strittmatter, SM
    [J]. CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (01) : 89 - 94
  • [19] Fatality in mice due to oversaturation of cellular microRNA/short hairpin RNA pathways
    Grimm, Dirk
    Streetz, Konrad L.
    Jopling, Catherine L.
    Storm, Theresa A.
    Pandey, Kusum
    Davis, Corrine R.
    Marion, Patricia
    Salazar, Felix
    Kay, Mark A.
    [J]. NATURE, 2006, 441 (7092) : 537 - 541
  • [20] HOPKINSONWOOLLEY J, 1994, J CELL SCI, V107, P1159