Miller D J, Asakura K, Rodriguez M
Department of Immunology, Mayo Clinic and Foundation, Rochester, Minnesota 55905, USA.
J Neurosci Res. 1995 Jun 15;41(3):291-6. doi: 10.1002/jnr.490410302.
The destruction of central nervous system (CNS) myelin, the lipid-rich insulator surrounding axons in the mammalian brain and spinal cord, is the primary pathological finding in multiple sclerosis. Myelin loss can result in a significant clinical deficit, and was originally thought to be permanent, similar to axonal destruction. However, myelin regeneration is now an established phenomenon in both human disease and animal models of CNS demyelination. In this review, the concept of remyelination in demyelinating diseases such as multiple sclerosis is discussed and the usefulness of animal models of CNS demyelination in developing experimental strategies to promote remyelination is examined. Special emphasis is given to the Theiler's murine encephalomyelitis model, which has been the primary animal model used to investigate therapies designed specifically to stimulate myelin repair.
中枢神经系统(CNS)髓鞘的破坏是多发性硬化症的主要病理学发现,髓鞘是哺乳动物脑和脊髓中围绕轴突的富含脂质的绝缘体。髓鞘丢失可导致严重的临床缺陷,最初被认为是永久性的,类似于轴突破坏。然而,髓鞘再生现在已成为人类疾病和中枢神经系统脱髓鞘动物模型中的既定现象。在这篇综述中,我们讨论了脱髓鞘疾病(如多发性硬化症)中髓鞘再生的概念,并研究了中枢神经系统脱髓鞘动物模型在开发促进髓鞘再生的实验策略中的作用。特别强调了泰勒氏鼠脑脊髓炎模型,它一直是用于研究专门刺激髓鞘修复疗法的主要动物模型。