骨关节炎影响哺乳动物的卵子生成:胶原酶诱导的骨关节炎对小鼠卵母细胞骨架的影响。

IF 2.6 Q3 IMMUNOLOGY International Journal of Inflammation Pub Date : 2021-11-09 eCollection Date: 2021-01-01 DOI:10.1155/2021/8428713
Anton Ivanov Kolarov, Irina Valcheva Chakarova, Valentina Prodanova Hadzhinesheva, Venera Pantaleeva Nikolova, Stefka Metodieva Delimitreva, Maya Dyankova Markova, Ralitsa Stefanova Zhivkova
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引用次数: 0

摘要

作为一种主要影响女性的老年退行性关节疾病,骨关节炎可在年轻和积极工作的人群中发展,因为涉及关节负荷和损伤的活动。小鼠模型中的胶原酶诱导骨关节炎(CIOA)使我们首次研究了其对排卵小鼠卵母细胞关键细胞骨架结构(减数分裂纺锤体和肌动蛋白分布)的影响。免疫荧光法分析了它们的减数分裂纺锤体、肌动蛋白帽和染色质。共获得来自CIOA小鼠的193个卵母细胞和来自对照动物的209个卵母细胞,几乎全部处于中期I (m1)或中期II (MII)。CIOA患者的成熟率(26.42%)低于对照组(55.50%)。CIOA患者的卵母细胞纺锤体明显较大(平均为37 μm,而对照组为25 μm, p < 0.001), CIOA患者的大纺锤体比例超过64%,而对照组为15% (p < 0.001)。CIOA卵母细胞的减数分裂纺锤体宽度为68.35%和54.90%(平均18.04 μm I和17.34 μm II),与对照组(11.64 μm I和12.64 μm II)相比,CIOA卵母细胞减数分裂纺锤体的极宽(平均6.9 μm)约为对照组(3.6 μm)的两倍。CIOA卵母细胞常含有定向失稳的微管。超过91%的对照组和不到20%的CIOA卵母细胞可见肌动蛋白帽。许多没有肌动蛋白帽的CIOA卵母细胞外周肌动蛋白环呈非极化厚(m1占61.87%,m2占52.94%),两组染色体排列正常的比例均超过82%。综上所述,CIOA影响了排卵小鼠卵母细胞的细胞骨架,减数分裂纺锤体变长变宽,极变宽,纤维紊乱,肌动蛋白帽被一个宽的非极化环所取代。然而,减数分裂纺锤体在CIOA卵母细胞中成功形成,即使在异常情况下,也允许染色体正确排列。
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Osteoarthritis Affects Mammalian Oogenesis: Effects of Collagenase-Induced Osteoarthritis on Oocyte Cytoskeleton in a Mouse Model.

Known as a degenerative joint disorder of advanced age affecting predominantly females, osteoarthritis can develop in younger and actively working people because of activities involving loading and injuries of joints. Collagenase-induced osteoarthritis (CIOA) in a mouse model allowed us to investigate for the first time its effects on key cytoskeletal structures (meiotic spindles and actin distribution) of ovulated mouse oocytes. Their meiotic spindles, actin caps, and chromatin were analyzed by immunofluorescence. A total of 193 oocytes from mice with CIOA and 209 from control animals were obtained, almost all in metaphase I (M I) or metaphase II (MII). The maturation rate was lower in CIOA (26.42% M II) than in controls (55.50% M II). CIOA oocytes had significantly larger spindles (average 37 μm versus 25 μm in controls, p < 0.001), with a proportion of large spindles more than 64% in CIOA versus up to 15% in controls (p < 0.001). Meiotic spindles were wider in 68.35% M I and 54.90% M II of CIOA oocytes (mean 18.04 μm M I and 17.34 μm M II versus controls: 11.64 μm M I and 12.64 μm M II), and their poles were approximately two times broader (mean 6.9 μm) in CIOA than in controls (3.6 μm). CIOA oocytes often contained disoriented microtubules. Actin cap was visible in over 91% of controls and less than 20% of CIOA oocytes. Many CIOA oocytes without an actin cap had a nonpolarized thick peripheral actin ring (61.87% of M I and 52.94% of M II). Chromosome alignment was normal in more than 82% in both groups. In conclusion, CIOA affects the cytoskeleton of ovulated mouse oocytes-meiotic spindles are longer and wider, their poles are broader and with disorganized fibers, and the actin cap is replaced by a broad nonpolarized ring. Nevertheless, meiotic spindles were successfully formed in CIOA oocytes and, even when abnormal, allowed correct alignment of chromosomes.

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