大鼠肝再生过程中碱性磷酸酶活性变化及其超微细胞化学研究

目的 研究2／3肝切除后大鼠肝再生过程中碱性磷酸酶(AKP)活性的变化及其细胞定位。方法 利用比色法对AKP活性进行定量分析；用酶的原位复性电泳技术分析再生肝中AKP的种类和活性变化；用电镜细胞化学方法研究酶定位。结果 在肝部分切除后的肝再生期间，AKP出现两个活性高峰(16h和19h)，在每个活性高峰后，AKP均有显著下降；获得3种肝型AKP同工酶(140、160和180kD)，其中180kD的AKP只在肝再生过程中出现；随着肝再生的进展，AKP活性出现在细胞的不同部位。结论 AKP在肝再生过程中起重要作用，可能参与细胞代谢、物质转运、DNA合成和细胞分化。     

人工组织神经移植物修复狗缺损坐骨神经后腓肠肌的形态观察

目的 了解复合型医用可降解材料制成的人工组织神经移植物辅加神经再生素修复狗坐骨神经缺损后，腓肠肌的形态变化。方法 将人工组织神经移植物连接在狗的坐骨神经缺损30mm处。以自体神经桥接和神经缺损的狗为对照组Ⅰ和Ⅱ。术后6个月时取腓肠肌进行称重、特殊染色和组织化学染色，显微镜下了解腓肠肌的形态变化并进行图像定量分析，同时了解肌纤维的超微结构变化。结果 术后6个月，实验组腓肠肌的萎缩形态指标变化均轻于对照组Ⅱ，而与对照组Ⅰ相似。结论 经人工组织神经移植物修复缺损的坐骨神经后，使腓肠肌又重新获得神经支配，肌肉萎缩明显减轻。     

Disconnected optic axons persist in the visual pathway during regeneration of the retino-tectal projection in the frog

Summary In this study, we crushed one optic nerve in the frog Litoria (Hyla) moorei and at intervals thereafter anterogradely labelled optic axons with horseradish peroxidase (HRP). For one series, HRP was applied between the eye and the crush site and in a second series between the crush site and the chiasm. A tectal projection of regenerating axons was seen in both series but, in addition, up to 12 weeks post-crush, the second series displayed an additional projection. Its appearance matched that of the disconnected, but persisting, optic axon terminals which are found after enucleation or optic nerve ligation. We conclude that, in the frog, many disconnected optic axons persist throughout the period of optic nerve regeneration and of restoration of an orderly retino-tectal map.Abbreviation HRP horseradish peroxidase     

Effect of Phosphatidylcholine Liposome on Regeneration of Surgical Wound in Guinea Pig Lung

Phosphatidylcholine liposomes in a dose of 25 mg/kg displayed wound-healing properties. They increased the count of alveolar macrophages, lymphocytes, and microvessels in damaged regions and, therefore, attenuated emphysematous changes in the lungs.     

隔膜条件下骨再生成骨细胞来源的实验观察

目的:研究在隔膜条件下引导性骨再生过程中成骨细胞的来源,进一步认识引导性骨再生的机制.方法:以成年新西兰兔为研究对象,在双侧挠骨中段制作标准骨缺损不愈合模型,用硅胶膜成管状包裹一侧骨缺损,另一侧无特殊处理为对照.术后分别进行X线检查、常规HE染色以及SP方法BMP、BGP抗体的免疫组化染色.结果:硅胶膜在骨缺损处形成隔离密闭的腔室,将周围组织阻挡于骨缺损之外.早期骨端骨内膜、骨髓基质细胞大量增殖,形成肉芽组织占据骨缺损.骨再生过程中表现出明显的组织学特征:骨痂表面为2～3层成骨细胞,骨缺损中央为肉芽组织,两者之间为数层细胞形成的移行区,细胞排列疏松.早期骨端骨内膜、骨髓基质细胞BMP、BGP呈强阳性染色,骨痂生长过程中,移行区部分细胞呈阳性染色.结论:结果表明在隔膜条件下骨再生的成骨细胞在早期来源于髓内的骨内膜和骨髓基质细胞,骨痂形成后,成骨细胞则来源于骨内膜、骨髓、骨膜增殖细胞共同形成的肉芽组织中的间质细胞或成纤维细胞.     

Satellite cells express the trophic factor IGF-I in regenerating skeletal muscle

The expression of insulin-like growth factor I (IGF-I, somatomedin C) was studied in regenerating skeletal muscle. Irreversible damage to skeletal muscle cells was induced in the extensor digitorum longus muscle (EDL) of adult rats by ischaemia, preceded by glycogen depletion, and the regeneration process was studied for periods up to 14 days after injury. The IGF-I was demonstrated by indirect immunofluorescence. Immunoreactivity against ribonucleotide reductase (RR) was used as a marker for DNA synthesis, that is, cell proliferation. Increased IGF-I immunoreactivity could be demonstrated within 24h after injury in satellite cells, intramuscular nerves and in blood vessels. The IGF-I immunoreactivity remained virtually unchanged in the contralateral, undamaged EDL. An increasing number of satellite cells, expressing high IGF-I immunoreactivity, could be demonstrated in the injured EDL, and within 72 h myoblasts, expressing high IGF-I and RR immunoreactivity, were formed. Small immature muscle cells, displaying high IGF-I immunoreactivity, were observed 4 days after injury. Increased IGF-I immunoreactivity was still obvious in the regenerated muscle cells 14 days after injury while RR immunoreactivity was seen only in scattered satellite cells. It is concluded that IGF-I may act as a trophic factor during regeneration of skeletal muscle after injury.     

大鼠再生肝对二乙基亚硝胺启动作用的敏感性

目的比较再生肝和正常肝对二乙基亚硝胺（ＤＥＮ）启动作用的敏感性。方法以２／３肝叶切除后８周末的大鼠为实验组,正常大鼠为对照组,作如下比较：肝重、常规组织学检查及３Ｈ－ＴｄＲ掺入试验;用修改的Ｓｏｌｔ－Ｆａｒｂｅｒ模型,通过对ＧＧＴ阳性癌前病灶的体视学测量,观察肝脏对ＤＥＮ的启动效应;在体内和体外（无血清原代培养肝细胞）经ＤＥＮ攻击后,以核酸原位缺口标记方法观察肝细胞ＤＮＡ的损伤程度。结果２／３肝叶切除后８周末的实验组肝脏的修复过程已完成,未见肝细胞继续增生的表现;经ＤＥＮ攻击后,实验组肝癌前病灶在数密度和体积密度上都显著高于对照组;无论在体内或体外接受ＤＥＮ攻击后,实验组肝细胞ＤＮＡ的损伤程度都显著大于对照组。结论即使再生过程已经完成,再生肝仍比正常肝具有较高的致癌敏感性,这与再生肝肝细胞在ＤＥＮ攻击后其ＤＮＡ损伤较重相关。     

Electron-autoradiographic study of RNA synthesis in epithelial cells of the renal tubules of albino rats poisoned with mercuric chloride

Department of Biology, Grodno Medical Institute. Department of Pathological Anatomy, A. V. Vishnevskii Institute of Surgery, Academy of Medical Sciences of the USSR, Moscow. (Presented by Academician of the Academy of Medical Sciences of the USSR D. S. Sarkisow.) Translated from Byulleten' Éksperimental'noi Biologii i Meditsiny, Vol. 107, No. 3, pp. 357–360, March, 1989.     

Lectin binding and desmin expression during necrosis, regeneration, and neurogenic atrophy of human skeletal muscle

Changes in the cytoplasm of skeletal muscle fibres during necrosis, regeneration, and neurogenic atrophy have been studied in a wide range of human neuromuscular diseases with a panel of eleven biotinylated lectins and by immunohistochemical staining for the cytoskeletal protein desmin. Increased binding of several lectins was observed in both necrotic and regenerating fibres, with Concanavalin A the most consistently positive lectin. Staining for desmin was strong in the cytoplasm of regenerating and partially damaged fibres and was lost in necrotic fibres, although there were differences in the staining reactions of the two antidesmin antibodies used. In fibres which had undergone neurogenic atrophy, cytoplasmic lectin binding was seen only with Griffonia simplicifolia 1 lectin, and desmin was expressed more strongly than in normal fibres. Lectin binding and immunohistochemical staining from desmin can supplement the information obtained from muscle biopsies by conventional histochemical methods and lead to a better understanding of the mechanisms of muscle damage.     

Expression pattern of Popdc2 during mouse embryogenesis and in the adult.

The Popdc2 gene is a member of the Popeye domain containing gene family encoding membrane proteins with prominent expression in striated and smooth muscle tissue. After introducing a LacZ reporter gene into the Popdc2 locus, expression was studied during embryonic development and postnatal life. At embryonic day (E) 7.5, expression was present in cardiac and extraembryonic mesoderm. At E10.5, expression was found in heart, somites, and mesothelial cells lining the coelom. At E12.5, expression was present in the coelomic mesothelium, pericardial and myocardial layer of the heart, skeletal muscle, bladder, gut, and umbilical vessels. Postnatal expression was found in cardiac and skeletal muscle and in the smooth muscle layer of colon, rectum, and bladder. In the stomach, Popdc2 was exclusively present in the pyloric epithelium. In conclusion, Popdc2 is expressed in various muscle and nonmuscle cell types during embryonic development and in postnatal life.