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32 results about "Cardiac Progenitor Cell" patented technology

Cd82-positive cardiac progenitor cells

An object of the present invention is to provide a myocardial progenitor cell that is specifically induced to differentiate into a cardiomyocyte, and a method for preparing the myocardial progenitor cell. A method for preparing a CD82-positive cell includes, in sequence, a step (a) of obtaining stem cells, a step (b) of subjecting the stem cells to induction treatment of differentiation into cardiovascular cells, and a step (c) of separating, from the stem cells having been subjected to the induction treatment of differentiation in the step (b), a CD82-positive cell being negative for at least one cell surface marker selected from CD73, CD44, CD105, CD121a, CD18, and CD120a. This method enables preparation of a CD82-positive cell for use as a myocardial progenitor cell.
Owner:KYOTO UNIV MED PHARM COLLABORATION BUILDING

Three-dimensional structure for cardiac muscular tissue regeneration and manufacturing method therefor

The present invention provides a preparation method of a three-dimensional construct for regenerating a cardiac muscle tissue comprising; a step of forming a three-dimensional construct by printing and crosslinking the first bioprinting composition comprising a tissue engineering construct forming solution containing decellularized extracellular matrix and a crosslinking agent, and cardiac progenitor cells, and the second bioprinting composition comprising the tissue engineering construct forming solution, mesenchymal stem cells and a vascular endothelial growth factor, to arrange the first bioprint layer and the second bioprint layer alternately; and a step of obtaining a crosslink-gelated three-dimensional construct by thermally gelating the crosslinked three-dimensional construct, and a three-dimensional construct for regenerating a cardiac muscle tissue, and the preparation method according to the present invention not only equally positions the cardiac progenitor cells in the construct but also implements a vascular network composed of vascular cells in the construct, so that the viability of cells can be maintained for a long time and the cell transfer efficiency into the myocardium can be significantly improved.
Owner:T&R BIOFAB

Three-dimensional structure for cardiac muscular tissue regeneration and manufacturing method therefor

Provided are a method for manufacturing a three-dimensional structure for cardiac muscular tissue regeneration, and a three-dimensional structure for cardiac muscular tissue regeneration, the method comprising the steps of: forming a three-dimensional structure by printing and crosslinking with a first bioprinting composition and a second bioprinting composition so as to alternately arrange a first bioprinted layer and a second bioprinted layer, wherein the first bioprinting composition contains cardiac progenitor cells and a tissue engineering structure formation solution containing decellularized extracellular matrix and a crosslinking agent, and the second bioprinting composition contains a tissue engineering structure formation solution, mesenchymal stem cells, and a vascular endothelial growth factor; and obtaining a crosslinked-gelled three-dimensional structure by performing thermal gelation on the crosslinked three-dimensional structure. The manufacturing method according to the present invention can uniformly position cardiac progenitor cells in the structure and maintain the viability of cells for a long time by implementing a blood vessel network composed of vascular cells in the structure, thereby remarkably improving the efficiency of cellular delivery into the myocardium.
Owner:T&R BIOFAB

Technique for heart disease external differentiation therapy by utilizing stem cells of masticatory muscles and orbicularis oculi muscles

InactiveCN102703382AArtificial cell constructsUnknown materialsCoronary artery guide catheterNon invasive
The invention belongs to the field of adult stem cells and regenerative medicine, and relates to the techniques of adult stem cell extraction, external expansion and differentiation induction as well as stem cell transplantation. The techniques are based on the theory that head and facial masticatory muscles have the same origin with cardiac progenitor cells. As shown by the analysis on the genetic expression, cardiac muscle genes Nk*2.5 and Isl1 in the masticatory muscle stem cells have expressions of different degrees. The techniques utilize that the masticatory muscle stem cells have the characteristics of the cardiac muscle stem cells, collect a masticatory muscle sample by the non-invasive biopsy method, and externally expands the masticatory muscle stem cells by the suspension culture method; and non-coding micro RNA (ribonucleic acid) is adopted to change the masticatory muscle stem cells and facilitate differentiation and purification of the masticatory muscle stem cells into the heart muscle cells. The transplantation of the purified cardiac muscle cells to a part with myocardial infarction is performed by means of the coronary artery duct injection or the cell membrane technique (the cell membrane is placed on the surface of myocardial infarction organization), so that the myocardial infarction or the ischemic heart disease can be cured.
Owner:珠海霍普金斯医药研究院股份有限公司

Method for regulating and controlling conduction velocity of tissue-engineered conduction bundle and application

PendingCN114854693AEffective in regulating conduction velocityImprove precision controlPeptidesSkeletal/connective tissue cellsHeart cellsPost transplant
The invention provides a method for regulating and controlling the conduction velocity of a tissue-engineered conduction bundle and application. By changing the cell planting density and the tissue culture period in the tissue engineering heart conduction bundle construction and culture process, it is found that the conduction speed is regulated and controlled most effectively when the planting density is 1 * 10 < 7 >-1.1 * 10 < 7 > cells / ml and the culture period is 2 weeks. On the basis of the parameters, heart cells overexpressing Tbx3 and common heart progenitor cells are jointly planted on a collagen sponge stent to construct ECT, and it is found that the effect of precise regulation and control of the conduction velocity is better through the matching of 70-80% of Tbx3 + H9C2 cells and 20-30% of Tbx3-H9C2 cells. The conduction velocity of the ECT constructed by the method is close to the in-vivo atrioventricular junction level, the key problem of realizing physiological atrioventricular electrical conduction in the process of reconstructing an atrioventricular pathway through a tissue engineering conduction bundle (ECT) is solved, namely, the problem of how to ensure atrioventricular extension after ECT transplantation is solved, and an effective method is provided for regulating and controlling the conduction velocity of the ECT.
Owner:THE NAVAL MEDICAL UNIV OF PLA

Composition for cell transplant, and method for cell transplant

Provided are a composition for cell transplant and a method for cell transplant that allow myocytes and / or cardiac progenitor cells to be suitably maintained in myocardial tissue and allow the survival and proliferation of transplanted cells to be improved. This composition for cell transplant comprises cells and an aqueous solution of a protein (A), and is characterized in that: the cells are myocardial cells and / or cardiac progenitor cells; protein (A) has a hydrophobicity of 0.2-1.2; the protein (A) has a polypeptide chain (Y) and / or a polypeptide chain (Y'); the total number of polypeptidechains (Y) and polypeptide chains (Y') in the protein (A) is 1-100; the polypeptide chain (Y) is an amino acid sequence (X) repeated 2-100 times, the amino acid sequence being any one of a VPGVG sequence (1) which is an amino acid sequence represented by SEQ ID NO:1, a GVGVP sequence (2) which is an amino acid sequence represented by SEQ ID NO:2, a GPP sequence, a GAP sequence, and a GAHGPAGPK sequence (3), which is an amino acid sequence represented by SEQ ID NO:3; the polypeptide chain (Y') is the polypeptide chain (Y) where 0.1-5% of the amino acid residues thereof are substituted with lysine residues and / or arginine residues; and the total number of the lysine residues and arginine residues is 1-100.
Owner:KYOTO UNIV +1

Composition for cell transplant, and method for cell transplant

Provided are a composition for cell transplant and a method for cell transplant, both of which enable a myocardial tissue to favorably retain cardiac myocytes and/or cardiac progenitors and can improve the persistence and proliferation of transplanted cells. The composition for cell transplant of the present invention is a composition for cell transplant, containing cells and an aqueous solution containing a protein (A), the cells including a cardiac myocyte and/or a cardiac progenitor, the protein (A) having a degree of hydrophobicity of 0.2 to 1.2, the protein (A) containing a polypeptide chain (Y) and/or a polypeptide chain (Y′), the protein (A) containing 1 to 100 polypeptide chains as a total of the polypeptide chain (Y) and the polypeptide chain (Y′), the polypeptide chain (Y) being a polypeptide chain having 2 to 100 continuous amino acid sequences (X), the amino acid sequence (X) having any one of a VPGVG sequence (1) corresponding to an amino acid sequence of SEQ ID NO: 1, a GVGVP sequence (2) corresponding to an amino acid sequence of SEQ ID NO: 2, a GPP sequence, a GAP sequence, and a GAHGPAGPK sequence (3) corresponding to an amino acid sequence of SEQ ID NO: 3, the polypeptide chain (Y′) being a polypeptide chain having a structure in which 0.1 to 5% amino acid residues in the polypeptide chain (Y) are replaced by a lysine residue and/or an arginine residue and including 1 to 100 residues as a total of the lysine residue and the arginine residue.
Owner:KYOTO UNIV +1
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