Tarique Imran, Lu Tong, Tariq Mansoor
Department of Healthcare Biotechnology, Atta Ur Rehman School of Applied Biosciences, National University of Science and Technology, Islamabad, Pakistan; Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao 266237, China.
Shandong Provincial Key Laboratory of Animal Cell and Developmental Biology, School of Life Sciences, Shandong University, Qingdao 266237, China.
Micron. 2023 Jun;169:103446. doi: 10.1016/j.micron.2023.103446. Epub 2023 Mar 21.
Use of zebrafish as animal model for various diseases during early developmental stages has been exponentially increased with the aim to achieve the best representative results in this transparent fish. Recent studies documented that Rbm24a mutant causes cataract formation and resulted in blindness using the zebrafish model. Therefore, correct interpretation of studies that aimed for molecular approaches, a description of comparative and in-depth analysis of development of lens in wildtype and mutant is crucial to obtain the correct conclusion. In this study, we use a gold standard method the Transmission Electron Microscopy (TEM) to analysis the lens development in rbm24a mutant zebrafish. Firstly, we compare the cellular structures at 16-20 h post fertilization (hpf), the lens placode in ectoderm indicated delay lens development in rbm24a mutant than wildtype (siblings) zebrafish. At 33 hpf, loosely appeared lens fiber cells showed heterogenous electron density with numbers of mitochondria in lens of rbm24a mutant, revealed the influence of gene mutation in lens development. A detail ultrastructure of lens of rbm24a mutant also presented at 33 hpf. Comparatively in wildtype (siblings) at 33 hpf, lens exhibited homogenous electron density in tightly packed lens fiber cells with few mitochondria. Furthermore, to characterize the lens in rbm24a mutant we obtained data of cellular structures on 25 hpf and 1.5 days' post fertilization (dpf). At 25 hpf in mutant zebrafish, the detached solid sphere lens mass from ectoderm showed karyorrhexis, mitophagy and vesicles (also multivesicular bodies), these cellular structures supposed to hamper the development of future fiber cells. Moreover, at 1.5 dpf in mutant, nuclear excisosome, multilamellar bodies and irregular shaped mitochondria in heterogenous electron dense cytoplasm of lens fiber cells, collectively shown affected lens transparency. In summary the ultrastructure results of lens of rbm24a mutant zebrafish expand our knowledge and give reflection of different cellular activities like autophagy, apoptosis, vesicles (multivesicular bodies) and nuclear excisosomes which play their role in transparency achievement.
为了在这种透明鱼类中获得最具代表性的结果,斑马鱼作为各种疾病早期发育阶段动物模型的应用呈指数级增长。最近的研究表明,使用斑马鱼模型,Rbm24a突变体可导致白内障形成并导致失明。因此,对于旨在进行分子研究的实验结果进行正确解读,对野生型和突变体晶状体发育进行比较和深入分析的描述,对于得出正确结论至关重要。在本研究中,我们使用一种金标准方法——透射电子显微镜(TEM)来分析rbm24a突变体斑马鱼的晶状体发育。首先,我们比较了受精后16 - 20小时(hpf)的细胞结构,外胚层中的晶状体原基显示,与野生型(同胞)斑马鱼相比,rbm24a突变体的晶状体发育延迟。在33 hpf时,rbm24a突变体晶状体中松散出现的晶状体纤维细胞显示出异质电子密度,且有大量线粒体,这揭示了基因突变对晶状体发育的影响。在33 hpf时,还呈现了rbm24a突变体晶状体的详细超微结构。相比之下,在33 hpf的野生型(同胞)中,晶状体在紧密排列的晶状体纤维细胞中呈现均匀的电子密度,线粒体较少。此外,为了表征rbm24a突变体中的晶状体,我们获取了受精后25 hpf和1.5天(dpf)的细胞结构数据。在突变体斑马鱼受精后25 hpf时,从外胚层分离的实心球形晶状体团显示出核碎裂、线粒体自噬和囊泡(也有多泡体),这些细胞结构可能会阻碍未来纤维细胞的发育。此外,在突变体受精后1.5 dpf时,晶状体纤维细胞异质电子致密细胞质中的核外切体、多层小体和不规则形状的线粒体,共同表明晶状体透明度受到影响。总之,rbm24a突变体斑马鱼晶状体的超微结构结果扩展了我们的知识,并反映了自噬、凋亡、囊泡(多泡体)和核外切体等不同的细胞活动,它们在实现透明度方面发挥着作用。