Department of Ophthalmology and Visual Neurosciences, University of Minnesota Medical School, Minneapolis, Minnesota, United States.
Graduate Program in Molecular, Cellular, Developmental Biology and Genetics, University of Minnesota, Minneapolis, Minnesota, United States.
Invest Ophthalmol Vis Sci. 2021 Oct 4;62(13):3. doi: 10.1167/iovs.62.13.3.
Myoblast determination protein 1 (MYOD) is a critical myogenic regulatory factor in muscle development, differentiation, myofiber repair, and regeneration. As the extraocular muscles significantly remodel their myofibers throughout life compared with limb skeletal muscles, we hypothesized that the absence of MYOD would result in their abnormal structure and function. To assess structural and functional changes in the extraocular muscles in MyoD-/- mice, fiber size and number and optokinetic nystagmus reflex (OKN) responses were examined.
OKN was measured in MyoD-/- mice and littermate wild-type controls at 3, 6, and 12 months. The extraocular muscles were examined histologically for changes in mean myofiber cross-sectional area, total myofiber number, and nuclei immunostained for PAX7 and PITX2, markers of myogenic precursor cells.
The MyoD-/- mice developed nystagmus, with both jerk and pendular waveforms, in the absence and in the presence of moving visual stimulation. At 12 months, there were significant losses in mean myofiber cross-sectional area and in total number of orbital layer fibers in all rectus muscles, as well as in global layer fibers in the superior and inferior rectus muscles. Haploinsufficient mice showed abnormal OKN responses. PITX2-positive cell entry into myofibers of the MyoD-/- mice was significantly reduced.
This study is the first demonstration of the development of nystagmus in the constitutive absence of expression of the muscle-specific transcription factor MYOD. We hypothesize that myofiber loss over time may alter anterograde and/or retrograde communication between the motor nerves and extraocular muscles that are critical for maintaining normalcy of extraocular muscle function.
肌节决定蛋白 1(MYOD)是肌肉发育、分化、肌纤维修复和再生过程中的关键肌肉调节因子。由于与肢体骨骼肌相比,眼外肌在整个生命过程中显著重塑其肌纤维,我们假设 MYOD 的缺失将导致其结构和功能异常。为了评估 MyoD-/- 小鼠眼外肌的结构和功能变化,我们检查了纤维大小和数量以及视动性眼球震颤反射(OKN)反应。
在 3、6 和 12 个月时,测量 MyoD-/- 小鼠及其同窝野生型对照的 OKN。通过组织学检查眼外肌,观察平均肌纤维横截面积、总肌纤维数量以及免疫染色标记的肌源性前体细胞标志物 PAX7 和 PITX2 的核变化。
MyoD-/- 小鼠在没有和存在运动视觉刺激的情况下均出现眼球震颤,表现为急跳和摆动波形。在 12 个月时,所有直肌的平均肌纤维横截面积和眶层纤维总数以及上、下直肌的总层纤维总数均显著减少。半合子不足的小鼠表现出异常的 OKN 反应。PITX2 阳性细胞进入 MyoD-/- 小鼠肌纤维的数量显著减少。
本研究首次证明在肌肉特异性转录因子 MYOD 的组成性缺失的情况下,眼球震颤的发展。我们假设随着时间的推移肌纤维的丢失可能会改变运动神经和眼外肌之间的顺行和/或逆行通讯,这对于维持眼外肌功能的正常至关重要。