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A Therapeutically Relevant Culture System for Human Neural Stem-Cells and Oligodendrocytes


技術優勢

The invention utilizes proprietary, serum-free, animal free nutrient media formula to first to propagate NSCs. A second distinct media formula is used to induce cell lineage specification of neural stem cells into oligodendrocytes. High efficiency of cell induction from neural stem cell to oligodendrocyte fate: from NSCs, most cells become OL. The system also allows specification of hips and ES cells in a shorter period of time than previously reported in the literature. The culture system can be used in formation, propagation, and maintenance of NSCs in adherent cultures, i.e. in two-D cultures, or as neurospheres or oligospheres, i.e. three-dimensional cultures.


詳細技術說明

Neural stem cell propagation and fate specification. The novel culture system - developed by Dr. Araceli Espinosa-Jeffrey and colleagues in the Semel Institute for Neuroscience and Human Behavior - improves NSC propagation and specification into oligodendrocytes. The system relies on a series of chemically defined media, specifically designed and carefully characterized for each developmental stage in the OL lineage. Generation of OL precursors from this system could be used for cell-replacement therapies, which are not limited to therapeutic myelin regeneration after brain or spinal cord trauma or for treatment of genetic myelin disorders. The induced OL or OL precursors would also be valuable to biomedical research. ES and hips cell fate specification. The research team has modified the novel culture system to also allow the specification of ES and hiPS cells into the OL cell fate. The versatility of the system to induce these cell types to oligodendrocytes expands its utility as a research tool and improves compatibility for patient cell transplantation applications.


附加資料

Patent Number: US20120052577A1
Application Number: US13223164A
Inventor: Espinosa de los Monteros, Maria Dolores Araceli | de Vellis, Jean S.
Priority Date: 31 Aug 2010
Priority Number: US20120052577A1
Application Date: 31 Aug 2011
Publication Date: 1 Mar 2012
IPC Current: C12N0005079 | C12N0005071
US Class: 435377 | 435406
Assignee Applicant: The Regents of the University of California
Title: CULTURE SYSTEM FOR STEM CELL PROPAGATION AND NEURAL AND OLIGODENDROCYTE SPECIFICATION
Usefulness: CULTURE SYSTEM FOR STEM CELL PROPAGATION AND NEURAL AND OLIGODENDROCYTE SPECIFICATION
Summary: The nutrient formula, culture medium, and cell culture are useful for propagating stem cells; for inducing specification of NSC to OL phenotype; and for inducing specification of multipotent stem cells to oligodendrocyte progenitors (all claimed). The nutrient formula, culture medium, and cell culture can also be used for cell replacement therapies (e.g. for treatment of brain and/or spinal cord injury, myelin disorders, and many neurodegenerative disorders).


主要類別

生物醫學


細分類別

DNA /基因工程


申請號碼

20120052577


其他

State Of Development

Researchers have described, tested, and validated these novel culture systems on human pluripotent and neural stem cells. 

Background

The production, culture, and harvest of stem cells are essential components of cell-replacement therapies that hold great promise in treating a variety of human diseases. Current methods of propagating and fate specifying stem cells are hampered by slow cell growth and poor efficiency. The vast majority of stem cells often do not reach the desired cell type. Therefore, there is a need to develop more efficient culture and induction methods for stem cells. Such improvements hold a particularly great potential for advancing research and treatment of neurodegenerative disorders or neurological trauma, both of which lack effective therapies.     

Related Materials

Espinosa-Jeffrey A, Wakeman DR, Kim SU, Snyder EY, de Vellis J. Culture system for rodent and human oligodendrocyte specification, lineage progression, and maturation. Curr Protoc Stem Cell Biol. 2009 Sep; Chapter 2: Unit 2D.4. PMID: 19725014.


Tech ID/UC Case

23181/2011-068-0


Related Cases

2011-068-0


國家/地區

美國

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