US2023212241A1PendingUtilityA1

Peptide for Inducing Regeneration of Tissue and Use Thereof

Assignee: STEMRIM INCPriority: Apr 26, 2011Filed: Dec 21, 2022Published: Jul 6, 2023
Est. expiryApr 26, 2031(~4.8 yrs left)· nominal 20-yr term from priority
C07K 14/4705C07K 2319/50C12N 2510/00C12N 15/85A61K 38/1709C07K 2319/21C07K 14/4702A61K 38/17A61P 1/00A61P 1/04A61P 1/16A61P 1/18A61P 11/00A61P 13/00A61P 15/00A61P 17/00A61P 17/02A61P 17/14A61P 19/00A61P 21/00A61P 25/00A61P 43/00A61P 9/00A61P 9/10A61K 35/15A61K 35/28A61K 48/00C07K 14/4718C12N 5/0647C12N 5/0663
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Claims

Abstract

(Objective) An objective of the present invention is to provide therapeutic agents that, in association with stimulation of PDGFRα-positive cells such as bone marrow mesenchymal stem cells, promote their mobilization into blood and accumulation in a damaged tissue, and induce tissue regeneration in a living body.(Means for solution) Multiple peptides were synthesized, and the migration-promoting activity of each peptide was evaluated. As a result, the present inventors successfully identified multiple peptides that have migration-promoting activity on a PDGFRα-positive bone marrow mesenchymal stem cell line (MSC-1). Further, the present inventors confirmed that the identified peptides also have migration-promoting activity on skin fibroblasts, which are PDGFRα-positive cells.

Claims

exact text as granted — not AI-modified
1 . A peptide comprising the amino acid sequence of position 17 to position 25 in the amino acid sequence of SEQ ID NO: 1 and having an activity of stimulating migration of a cell, wherein the peptide consists of 195 amino acids or less. 
     
     
         2 . The peptide of  claim 1 , which is a peptide consisting of 185 amino acids or less. 
     
     
         3 . The peptide of  claim 1 , which is a peptide consisting of 84 amino acids or less. 
     
     
         4 . The peptide of  claim 1 , which is a peptide consisting of 44 amino acids or less. 
     
     
         5 . The peptide of  claim 1 , which comprises the amino acid sequences of position 13 to position 25 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         6 . The peptide of  claim 1 , which comprises the amino acid sequences of position 10 to position 25 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         7 . The peptide of  claim 1 , which comprises the amino acid sequences of position 11 to position 44 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         8 . The peptide of  claim 1 , which comprises the amino acid sequences of position 11 to position 34 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         9 . The peptide of  claim 1 , which comprises the amino acid sequences of position 17 to position 30 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         10 . The peptide of  claim 1 , which comprises the amino acid sequences of position 14 to position 30 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         11 . The peptide of  claim 1 , which comprises the amino acid sequences of position 11 to position 30 in the amino acid sequence of SEQ ID NO: 1. 
     
     
         12 . The peptide of  claim 1 , which is a synthetic peptide. 
     
     
         13 . The peptide of  claim 1 , which is a peptide produced using a cell. 
     
     
         14 . The peptide of  claim 1 , which is a peptide to which a tag is added. 
     
     
         15 . The peptide of  claim 1 , which is a peptide to which a tag-derived peptide fragment is added. 
     
     
         16 . A composition comprising the peptide of  claim 1  and a pharmaceutically acceptable carrier or additive. 
     
     
         17 . The composition of  claim 16 , wherein the pharmaceutically acceptable carrier or additive is selected from the group consisting of surfactant, excipient, colorant, perfume, preservative, stabilizer, buffer, suspending agent, isotonizing agent, binder, disintegrant, lubricant, flow promoter, and flavoring agent. 
     
     
         18 . The composition of  claim 16 , wherein the pharmaceutically acceptable carrier or additive is selected from the group consisting of light anhydrous silicic acid, lactose, crystalline cellulose, mannitol, starch, carmellose calcium, carmellose sodium, hydroxypropylcellulose, hydroxypropylmethylcellulose, polyvinylacetaldiethylamino acetate, polyvinylpyrrolidone, gelatin, medium-chain fatty acid triglyceride, polyoxyethylene hydrogenated castor oil 60, white sugar, carboxymethyl cellulose, corn starch, and inorganic salt. 
     
     
         19 . A DNA encoding the peptide of  claim 1 . 
     
     
         20 . A vector comprising the DNA of  claim 19 . 
     
     
         21 . A transformed cell comprising the DNA of  claim 19 . 
     
     
         22 . A transformed cell comprising the vector of  claim 20 .

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