Method for identification of somatic stem cells
The invention relates to a method for identification of somatic stem cells, wherein the spatial arrangement of epitopes in a sample is captured by MELC technology for identifying the phenotype specific to the somatic stem cells. The invention moreover relates to a composition, a kit and a biochip comprising at least one antibody and/or ligand which can be employed for the performance of the method.
1 . Method for identification of somatic stem cells, wherein the spatial arrangement of epitopes in a sample is captured by MELC technology for identifying the phenotype specific to the somatic stem cells.
2 . Method according to claim 1 , wherein keratinocyte stem cells are identified by capturing the spatial arrangement of the epitopes Ki67, CD71, pan cytokeratin, CD29, CD49d in a tissue sample for identifying the phenotype “Ki67 off/ CD71 off/ pan cytokeratin on/ CD29 on/ CD49d on”, being specific to keratinocyte stem cells.
3 . Method according to claim 2 , characterized in that the tissue sample is a sample of the skin, in particular a section of skin tissue.
4 . Method according to claim 2 , characterized in that the tissue sample is a sample of the epidermis.
5 . Method according to claim 3 , characterized in that the tissue sample is a sample of the epidermis.
6 . Method according to claim 1 , characterized in that the spatial arrangement of the epitopes is captured by means of employing at least one particularly labeled antibody and/or ligand and/or biologics and/or a part of a biologics binding specifically to the epitopes.
7 . Method according to claim 1 , characterized in that at least one of the labelings is a fluorescent dye, in particular phycoerythrin or fluorescein, or quantum dot.
8 . Method according to claim 1 , characterized in that the spatial arrangement of the epitopes is captured by the sequence of the following method steps:
(a) applying a solution to the tissue sample;
(b) allowing the solution to take effect and removing the solution;
(c) recording an image prior to or after removing the solution;
wherein the solution contains at least one labeled antibody and/or ligand binding specifically to at least one of the epitopes.
9 . Method according to claim 8 , characterized in that steps (a) to (c) are repeated with at least one further solution which also contains at least one labeled antibody and/or ligand and/or at least one biologics and/or at least one part of a biologics specifically binding to at least one of the further epitopes, and
in that possibly subsequent to step (b) and/or (c) a washing step and/or subsequent to step (c) a bleaching step is performed.
10 . Method according to claim 2 , characterized in that at least one antibody is employed which is member of the following group:
7B11, an in particular fluorescein-labeled antibody which is directed against Ki67,
YDJ.1.2.2, an in particular fluorescein-labeled antibody which is directed against CD71,
MNF116, an in particular fluorescein-labeled antibody which is directed against pan cytokeratin,
4B7R, an in particular fluorescein-labeled antibody which is directed against CD29,
44H6, an in particular fluorescein-labeled antibody which is directed against CD49d.
11 . Method according to claim 6 , characterized in that at least one antibody is employed which is member of the following group:
7B11, an in particular fluorescein-labeled antibody which is directed against Ki67,
YDJ.1.2.2, an in particular fluorescein-labeled antibody which is directed against CD71,
MNF116, an in particular fluorescein-labeled antibody which is directed against pan cytokeratin,
4B7R, an in particular fluorescein-labeled antibody which is directed against CD29,
44H6, an in particular fluorescein-labeled antibody which is directed against CD49d.
12 . Method according to claim 1 , characterized in that the MELC robot technology is used for the detection of the specific phenotype.
13 . Composition or kit comprising at least one antibody and/or at least one ligand binding the epitopes Ki67, CD71, pan cytokeratin, CD29, CD49d specifically and being coupled each with in particular different labelings.
14 . Composition or kit according to claim 13 , characterized in that at least one of the labelings is a fluorescent dye, in particular phycoerythrin or fluorescein, or a quantum dot.
15 . Composition or kit according to claim 13 , characterized in that at least one antibody is a member of the following group:
7B11, an in particular fluorescein-labeled antibody which is directed against Ki67,
YDJ.1.2.2, an in particular fluorescein-labeled antibody which is directed against CD71,
MNF116, an in particular fluorescein-labeled antibody which is directed against pan cytokeratin,
4B7R, an in particular fluorescein-labeled antibody which is directed against CD29,
44H6, an in particular fluorescein-labeled antibody which is directed against CD49d.
16 . Composition or kit according to claim 14 , characterized in that at least one antibody is a member of the following group:
7B11, an in particular fluorescein-labeled antibody which is directed against Ki67,
YDJ.1.2.2, an in particular fluorescein-labeled antibody which is directed against CD71,
MNF116, an in particular fluorescein-labeled antibody which is directed against pan cytokeratin,
4B7R, an in particular fluorescein-labeled antibody which is directed against CD29,
44H6, an in particular fluorescein-labeled antibody which is directed against CD49d.
17 . Biochip for the detection of keratinocyte stem cells, wherein on one surface of the chip at least one ligand and/or at least one antibody binding specifically to the specific phenotype “Ki67 off/ CD71 off/ pan cytokeratin on/ CD29 on/ CD49d on” are coupled in such a way that their bondability to the phenotype is sustained.
18 . Use of the MELC robot technology for in-situ identification of somatic stem cells.