Compositions and methods for inducing myoblast differentiation and myotube formation
Provided herein are methods of inducing differentiation of a mammalian myoblast into a mammalian myocyte that include contacting a mammalian myoblast with an oligonucleotide that decreases Mitogen-activated protein kinase kinase kinase kinase 4 (Map4k4) mRNA expression in a mammalian myoblast or myocyte. Also provided are methods of inducing mammalian myoblasts or myocytes to form a myotube that include contacting two or more mammalian myoblasts or two or more mammalian myocytes with an oligonucleotide that decreases Map4k4 mRNA expression in a mammalian myoblast or myocyte. Also provided are methods of identifying a candidate agent useful for inducing muscle formation, and compositions containing an oligonucleotide that decreases Map4k4 mRNA expression in mammalian myoblast or myocyte and one or more additional muscle therapeutic agents and/or muscle-building neutraceuticals.
1. A method of inducing differentiation of a myoblast into a myocyte in a mammal having a muscle disorder, the method comprising:
a) selecting a mammal having a muscle disorder; and
b) administering to the selected mammal, an oligonucleotide selected from the group consisting of an inhibitory RNA, an antisense oligonucleotide, and a ribozyme that decreases Mitogen-activated protein kinase kinase kinase kinase 4 (Map4k4) mRNA expression in a mammalian myoblast, in an amount sufficient to induce differentiation of a myoblast into a myocyte in the selected mammal, wherein the oligonucleotide is modified at a base moiety, a sugar moiety, or phosphate backbone.
2. The method of claim 1 , wherein the selected mammal is a human.
3. The method of claim 1 , wherein the muscle disorder is selected from the group consisting of: muscle atrophy, muscle weakness, myopathy, chronic fatigue syndrome, fibromyalgia, muscular dystrophy, fatigue fibromyalgia, spinal muscle atrophy, distal muscular dystrophy, dermatomyositis, polymyositis, rhabdomyolysis, polymyalgia rheumatica, muscle tear, and claudication.
4. The method of claim 3 , wherein the selected mammal is a human.
5. The method of claim 1 , wherein administering the oligonucleotide results in treatment of the muscle disorder in the selected mammal.
6. The method of claim 1 , wherein the administering results in a decrease in the expression of Map4k4 mRNA in a myoblast in the selected mammal, and an increase in the expression of one or more of myogenic regulatory factor 5 (Myf5), creatine kinase, calsequestrin 1, peptidylarginine deiminase, and CD24a in a myoblast in the selected mammal.
7. A method of inducing myoblasts or myocytes in a mammal having a muscle disorder to form a myotube, the method comprising:
a) selecting a mammal having a muscle disorder; and
b) administering to the selected mammal, an oligonucleotide selected from the group consisting of an inhibitory RNA, an antisense oligonucleotide, and a ribozyme that decreases Mitogen-activated protein kinase kinase kinase kinase 4 (Map4k4) mRNA expression in a mammalian myoblast or myocyte, in an amount sufficient to induce two or more myoblasts and/or two or more myocytes in the selected mammal to form a myotube, wherein the oligonucleotide is modified at a base moiety, a sugar moiety, or phosphate backbone.
8. The method of claim 7 , wherein the selected mammal is a human.
9. The method of claim 7 , wherein the selected mammal has been diagnosed as having a muscle disorder.
10. The method of claim 7 , wherein the muscle disorder is selected from the group consisting of: muscle atrophy, muscle weakness, myopathy, chronic fatigue syndrome, fibromyalgia, muscular dystrophy, fatigue fibromyalgia, spinal muscle atrophy, distal muscular dystrophy, dermatomyositis, polymyositis, rhabdomyolysis, polymyalgia rheumatica, muscle tear, and claudication.
11. The method of claim 10 , wherein the selected mammal is a human.
12. The method of claim 7 , wherein administering the oligonucleotide to the selected mammal results in treatment of the muscle disorder.
13. The method of claim 1 , wherein the oligonucleotide is an inhibitory RNA.
14. The method of claim 13 , wherein the inhibitory RNA is a small inhibitory RNA.
15. The method of claim 7 , wherein the oligonucleotide is an inhibitory RNA.
16. The method of claim 15 , wherein the inhibitory RNA is small inhibitory RNA.