Generation of muscle lineage cells and therapeutic uses thereof
Methods and compositions for producing mature myotubes are provided herein. In some instances, the method involves contacting a myoblast in an in vitro culture with a compound, wherein the contacting the myoblast in the in vitro culture with the compound results in generation of mature myotubes or myotube-like cells. In some cases, methods of treatment are provided involving treating a subject with a compound such as a Chk1 inhibitor in order to treat muscle deficiency. The compound may be administered as a stand-alone therapy or in combination with a cell therapy, such as introduction of muscle precursor cells such as satellite cells or myoblasts. Methods for identifying compounds that induce formation of mature myotubes or myotube-like cells from myoblasts are also provided herein, as well as methods of using the identified compounds to treat subjects.
1. A method of generating mature myotubes, the method comprising:
a. providing myoblasts, wherein the myoblasts are derived from a human;
b. culturing the myoblasts in vitro in a culture comprising a medium comprising CHIR-124, thereby producing mature myotubes exhibiting two or more of the following features: (i) greater than 15 nuclei per myotube; (ii) a length greater than 0.5 mm; (iii) a diameter larger than 6 μm; and (iv) a myotube area greater than 3,000 μm 2 .
2. The method of claim 1 , further comprising incubating the myoblasts in the medium comprising CHIR-124 for at least 12 hours.
3. The method of claim 1 , further comprising detecting the mature myotubes in the culture.
4. The method of claim 1 , wherein the mature myotubes exhibit greater than 30 nuclei per cell.
5. The method of claim 1 , wherein the mature myotubes exhibit a myotube area greater than 4,000 μm 2 .
6. The method of claim 1 , wherein the mature myotubes exhibit a myotube area greater than 5,000 μm 2 .
7. The method of claim 1 , wherein the culture comprises myotubes with a mean myotube area greater than 1,000 μm 2 .
8. The method of claim 1 , wherein the culture comprises myotubes with a mean myotube area greater than 2,000 μm 2 .
9. The method of claim 1 , wherein the mature myotubes exhibit a diameter greater than 6 μm.
10. The method of claim 1 , wherein the mature myotubes exhibit a diameter greater than 10 μm.
11. The method of claim 1 , wherein the mature myotubes exhibit a diameter larger than 12 μm.
12. The method of claim 1 , wherein the mature myotubes exhibiting the two or more features make up at least 50% of a culture in the absence of purification or selection for mature myotubes.
13. The method of claim 1 , wherein the mature myotubes exhibiting the two or more features make up at least 50% of a culture in the absence of purification or selection for mature myotubes.
14. The method of claim 1 , wherein the mature myotubes exhibiting the two or more features make up at least 60% of the culture in the absence of purification or selection for mature myotubes and exhibit a diameter greater than 10 μm.
15. The method of claim 1 , wherein the myoblasts are primary myoblasts.
16. The method of claim 1 , wherein the myoblasts are generated by differentiating satellite cells in vitro.
17. The method of claim 1 , wherein the mature myotubes are mature myotube-like cells.
18. The method of claim 16 , wherein the satellite cells are generated by differentiating pluripotent stem cells in vitro.
19. The method of claim 18 , further comprising contacting satellite cells with a compound to generate the myoblasts.
20. The method of claim 19 , further comprising contacting pluripotent stem cells with one or more compounds to generate the satellite cells.
21. The method of claim 20 , wherein the mature myotubes are generated less than 30 days from the contacting the pluripotent stem cells with the one or more compounds to generate the satellite cells.
22. The method of claim 20 , wherein the mature myotubes are generated within 25 days from the contacting the pluripotent stem cells with the one or more compounds to generate the satellite cells.
23. The method of claim 20 , wherein the mature myotubes are generated less than 30 days from the contacting the pluripotent stem cells with the one or more compounds to generate the satellite cells and wherein the mature myotubes are generated at a rate of at least five mature myotubes per pluripotent stem cell.
24. The method of claim 20 , wherein the mature myotubes are generated less than 30 days from the contacting the pluripotent stem cells with the one or more compounds to generate the satellite cells and wherein the mature myotubes are generated at a rate of at least 50 mature myotubes per pluripotent stem cell.