Final answer:
In myasthenia gravis, the acetylcholine receptor at the neuromuscular junction is a nicotinic receptor and ligand-gated ion channel that becomes depolarized upon acetylcholine binding.
Step-by-step explanation:
Myasthenia gravis is an autoimmune disorder where antibodies target and block the function of the acetylcholine receptors at the neuromuscular junction, inhibiting muscle contraction. The cellular component affected by the disease in the patient's case is an acetylcholine receptor, which when acetylcholine binds to it, leads to depolarization of the membrane.
Hence, the true statements about the cellular component affected by myasthenia gravis are that it becomes depolarized when acetylcholine binds to it, it is a nicotinic receptor, and it is a ligand-gated ion channel.