Abstract:
본 발명은 NPC1 유전자가 신경줄기세포의 자체재생 및 분화에 관여한다는 새로운 기능규명에 근거한 것으로, 신경줄기세포의 자체재생 및 분화에 관여하는 NPC1 유전자, 상기 NPC1 유전자를 함유하는 유전자 전달체를 유효성분으로 포함하는 퇴행성 신경계 질환, 심근경색 등과 같은 줄기세포 재생 또는 분화 불량에 의한 질환 치료용 유전자치료제 및 상기 NPC1 유전자를 함유하는 신경줄기세포를 유효성분으로 포함하는 퇴행성 신경계 질환, 심근경색 등과 같은 줄기세포 재생 또는 분화 불량에 의한 질환 치료용 세포치료제에 관한 것이다. NPC1 유전자, 니이만 픽 병, 세포치료제
Abstract:
A pharmaceutical composition is provided to replace damaged liver cells using mesenchymal stem cell, to recover function of the liver and to prevent and treat a liver fibrosis or a liver sclerosis by reducing collagen fiber deposited in the liver. A composition for preventing and treating a liver fibrosis or a liver sclerosis includes mesenchymal stem cell originated from an umbilical cord blood or a fatty tissue. The umbilical cord blood or the fatty tissue is separated from human. A pharmaceutical composition for preventing and treating the liver fibrosis or the liver sclerosis includes the mesenchymal stem cell originated from the umbilical cord blood or the fatty tissue. The umbilical cord blood or the fatty tissue is separated from human.
Abstract:
A method for identifying an adult stem cell is provided to express Oct4, which is a marker to a multipotent stem cell, as well as Cripto-1, which is a marker for indifferentiation state, in the adult stem cell, thereby being useful for identifying more closely genuine adult stem cell. A method for identifying and isolating adult stem cells or tumor stem cells derived from human adipose tissue comprises the steps of: (a) immunostaining a group of adult stem cell or tumor stem cell candidates derived from the adipose tissue using an antibody binding to Cripto-1 and Oct4; (b) identifying the stem cell candidates group showing positive characteristic both on the Cripto-1 and Oct4 as the adult stem cells or tumor stem cells derived from the adipose tissue using a flow cytometer; and (c) isolating the identified stem cells.
Abstract:
A method for preparing a T-cell progenitor from a CD34 positive stem cell is provided to control the differentiation direction of a hematopoietic precursor in an STF(stem cell factor, Thrombopoietin, Flk-2/Flt3 ligand) medium, proliferate the T-cell progenitor in large scale and be useful for cell therapy relating to AIDS, cancer and auto-immune diseases. A method for preparing a T-cell progenitor from a CD34 positive stem cell comprises the steps of: (a) isolating CD34 positive stem cells derived from blood selected from the group consisting of human peripheral blood, bone marrow and cord blood; and (b) culturing and differentiating the isolated CD34 positive stem cells in a medium containing at least one cytokine selected from the group consisting of thrombopoietin(TPO), stem cell factor(SCF) and flk-2/flt3 ligand(FL) and not including thymic organ to obtain the T-cell progenitor showing negative immunological characteristic on CD2 and positive immunological characteristic on CD4, wherein the medium is an STF(stem cell factor, Thrombopoietin, Flk-2/Flt3 ligand) medium.
Abstract:
A multipotent stem cell derived from decidua or amnion isolated from human term placenta is provided to express both Oct4 and Cripto-1, be differentiated into mesenchymal stem cells, epithelial stem cells and neurons, thereby being applicable as a cell therapeutic agent due to excellent proliferation rate and being useful as a cell therapeutic agent of brain diseases such as Alzheimer's disease, Parkinson's disease, brain and spinal cord injury, and stroke. A method for preparing an adult stem cell comprises a step of culturing a pellet derived from amnion or decidua of human term placenta in a medium containing NAC(N-acetyl-L-cysteine) and then recovering the culture material, wherein the adult stem cell shows positive immunological characteristic on both Oct4 and Cripto-1 and has the ability of being differentiated into cells derived from endoderm, mesoderm and ectoderm and the adult stem cell derived from the amnion shows positive immunological characteristics on CD44, CD49b, CD73, CD90, CD24 and CD29 and negative immunological characteristics on CD4, CD33, CD34, CD45, CD62p, CD133, CD135 and HLA-DR. Further, the medium containing NAC(N-acetyl-L-cysteine) is a Keratinocyte-SFM(Serum-Free Medium) containing additionally an FBS(Fetal Bovine Serum), an ascorbic acid, a calcium, an rEGF(epidermal growth factor), a BPE(1,2-Bis (4-Pyridyl)Ethane), an insulin and a hydrocortisone.
Abstract:
본 발명은 개의 제대혈 및 개 태아의 심장 유래 다분화능 성체 줄기세포, 그 제조방법 및 이를 함유하는 세포 치료제에 관한 것으로, 더욱 자세하게는, 개의 제대혈 및 개 태아의 심장 유래 혈액에서 분리한 유핵세포를 FBS를 함유하는 배지에 배양하여 분리한 다분화능 성체 줄기세포, 그 제조방법 및 이를 함유하는 세포 치료제에 관한 것이다. 본 발명에 따른 성체 줄기세포는 개의 제대혈, 태반 및 개 태아의 심장에서 유래한 것으로서, 사람의 간엽세포 성격과 매우 유사한 성격을 가지고 있으면서도, 사람 제대혈 유래 간엽세포보다 초기 단계에 왕성한 세포 성장을 하므로 개의 난치병, 불치병 치료에 유용하게 사용될 수 있고, 골형성 세포 및 신경세포로 분화하는 능력을 가지고 있어, 근골격계 질환 및 뇌 신경계 질병 등의 치료에 유용하다. 제대혈, 태반, 성체 줄기세포, 다분화능
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Abstract:
An adult stem cell derived from canine cord blood, placenta and canine fetus heart is provided to be usefully used for treating incurable diseases of canine and be effective for treating musculoskeletal system disorders or neurological disorders, wherein the adult stem cell shows similar characteristic to mesenchymal cells of human, vigorously grows in an early stage and is differentiated into osteogenic cells and neurons. A method for preparing an adult stem cell comprises a step of culturing nucleated cells isolated from canine cord blood, placenta and canine fetus heart in DMEM containing 1-30% of FBS, wherein the adult stem cell shows at least one positive immunological characteristic regarding MHC CL, Thy.1 and CD44(BD) and negative immunological characteristic regarding CD34 at the same time, is attached to plastic to grow, has morphological characteristics of spindle-shape and is able to be differentiated into cells derived from endoderm, ectoderm, and mesoderm. A cell therapeutic agent for treating musculoskeletal system disorders or neurological disorders comprises the adult stem cell as an effective ingredient.
Abstract:
A DNA chip and a kit for screening substances showing activity as a peroxisome proliferator are provided to be able to rapidly and accurately screen the peroxisome proliferator inducing abnormal cell reaction in vivo, thereby being widely applied to safety test of various materials. The DNA chip for screening of peroxisome proliferator comprises: a probe consisting of 121 to 587 nucleotides, capable of binding specifically to a gene whose expression is induced by a peroxisome proliferators; a linker including oligo (dT)15, -(CH2)6- and amine group in sequence, whose 3'-terminal of oligo (dT)15 is linked to 5'-terminal of the probe; and a solid substrate, whose surface is coated with aldehyde group, connecting with amine group of the linker via Schiff's base reaction. In the DNA chip, the probe is at least one gene selected from SEQ ID Nos: 1 to 12. The kit for screening of peroxisome proliferator comprises the DNA chip and a fluorescence-labeled deoxynucleotide to be used for labeling cDNA synthesized from RNA isolated from a sample. The method for screening peroxisome proliferator using the kit comprises the steps of: (a) administering a peroxisome proliferator candidate chemical to an animal; (b) isolating RNA from the animal; (c) synthesizing fluorescence-labeled cDNA from the isolated RNA using fluorescence-labeled deoxynucleotide in the kit; (d) applying the synthesized cDNA to a DNA chip for screening peroxisome proliferator in the kit to allow hybridization; and (e) after washing the hybridized DNA chip, examining the hybridized probe in the DNA chip by using a scanner.
Abstract:
본 발명은 NPC1 유전자가 신경줄기세포의 자체재생 및 분화에 관여한다는 새로운 기능규명에 근거한 것으로, 신경줄기세포의 자체재생 및 분화에 관여하는 NPC1 유전자, 상기 NPC1 유전자를 함유하는 유전자 전달체를 유효성분으로 포함하는 퇴행성 신경계 질환, 심근경색 등과 같은 줄기세포 재생 또는 분화 불량에 의한 질환 치료용 유전자치료제 및 상기 NPC1 유전자를 함유하는 신경줄기세포를 유효성분으로 포함하는 퇴행성 신경계 질환, 심근경색 등과 같은 줄기세포 재생 또는 분화 불량에 의한 질환 치료용 세포치료제에 관한 것이다. NPC1 유전자, 니이만 픽 병, 세포치료제
Abstract:
A method for screening an anti-cancer material is provided to screen simply the anti-cancer material based on the finding of a human breast tumor stem cell not-expressing connexin 43, expressing Oct-4, an estrogen receptor and Cripto-1 and increasing the expression of estrogen, thereby screening a chemo-preventive agent and a therapeutic agent very rapidly at low cost without using a rodent model or an in vitro model and being usefully used for studying mechanism of a human breast cancer carcinogenesis. A method for screening an anti-cancer material comprises the steps of: (a) culturing an adult stem cell or a tumor stem cell derived from a human tissue to prepare a stem cell sphere; (b) treating the sphere with an anti-cancer candidate material; (c) identifying a stem cell marker such as Oct-4, Cripto-1, ABCG2, an estrogen receptor and connexin using an antibody or a gene coupled to the stem cell marker; and (d) selecting a material where the expression of the Oct-4, Cripto-1, ABCG2, and estrogen receptor is decreased or the expression of the connexin is increased, compared with a case of not-being treated with an anti-cancer candidate material as an anti-cancer material, wherein the human tissue derived adult stem cell is an adult stem cell derived from the human tissue selected from the group consisting of breast, bone marrow, umbilical cord blood, blood, liver, skin, gastrointestinal tract, placenta and uterus and the tumor stem cell is a tumor stem cell derived from a tumor selected from the group consisting of breast cancer, brain tumor, gastrointestinal tract cancer, lung cancer, liver cancer, uterine carcinoma, large intestine cancer and myelogenous leukemia.