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将成肌细胞植入组织不相容的小鼠体内(有无免疫抑制)的功能效应。

Functional effects of myoblast implantation into histoincompatible mice with or without immunosuppression.

作者信息

Wernig A, Irintchev A, Lange G

机构信息

Department of Physiology, University of Bonn, Germany.

出版信息

J Physiol. 1995 Apr 15;484 ( Pt 2)(Pt 2):493-504. doi: 10.1113/jphysiol.1995.sp020681.

DOI:10.1113/jphysiol.1995.sp020681
PMID:7602540
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1157910/
Abstract
  1. The goals of this study were to evaluate the immunogenicity of myogenic cells (MCs) (1) immediately after implantation into regenerating muscles, and (2) following their maturation under initial immunosuppression. Implanted mouse soleus muscles were evaluated by isometric tension recordings in vitro followed by histological investigations on frozen sections. 2. Implantation of non-histocompatible myoblasts into cryodamaged soleus muscles of CBA/J mice induced immune rejection which caused large and permanent deficits in muscle force: 4-42 weeks postimplantation maximal tetanic tension was 50-60% that of intact or regenerated cryodamaged control muscles without tendency for recovery or histological signs of muscle regeneration. Specific tension (force per unit muscle weight) was also significantly reduced. 3. On frozen sections, only 62 +/- 12% of the total area was desmin-positive, that is, occupied by muscle fibres, versus 90 +/- 4% in regenerated and 92 +/- 3% in intact muscles. Also, the total number of muscle fibre profiles was significantly reduced. 4. Under immune suppression with cyclosporin A (CsA), large muscles developed within 4 weeks. Following CsA withdrawal, muscle weight and force, in addition to desmin-positive areas on cross-sections, gradually declined over several months despite continual regeneration, indicating retarded immune rejection. 5. Initial application of CsA for 8 weeks after implantation, instead of 4 weeks, did not result in better survival of the implants, nor did a higher initial dose of CsA (100 instead of 50 mg kg-1 day-1). Prolonged continuous application of a reduced dose (25 mg kg-1 day-1) did not prevent muscle wasting but caused an additional delay. 6. It is concluded that histoincompatible myoblasts are highly immunogenic and that immune rejection causes large and permanent muscle deficits indicating elimination of host muscle tissue. Initial transient immunosuppression protects the incompatible cells, but after withdrawal, prolonged immune rejection and retarded muscle wasting occur.
摘要
  1. 本研究的目的是评估肌源性细胞(MCs)的免疫原性:(1)在植入再生肌肉后即刻;(2)在初始免疫抑制下成熟之后。通过体外等长张力记录评估植入的小鼠比目鱼肌,随后对冰冻切片进行组织学研究。2. 将非组织相容性成肌细胞植入CBA/J小鼠的冷冻损伤比目鱼肌中会引发免疫排斥反应,导致肌肉力量出现巨大且永久性的缺陷:植入后4 - 42周,最大强直张力仅为完整或再生的冷冻损伤对照肌肉的50 - 60%,且无恢复趋势或肌肉再生的组织学迹象。比张力(每单位肌肉重量的力量)也显著降低。3. 在冰冻切片上,总面积中只有62±12%为结蛋白阳性,即被肌纤维占据,而再生肌肉中这一比例为90±4%,完整肌肉中为92±3%。此外,肌纤维轮廓的总数显著减少。4. 在环孢素A(CsA)免疫抑制下,4周内发育出大肌肉。撤掉CsA后,尽管持续再生,但肌肉重量和力量以及横截面上结蛋白阳性区域在数月内逐渐下降,表明免疫排斥反应延迟。5. 植入后最初应用CsA 8周而非4周,并未使植入物有更好的存活情况,较高的初始CsA剂量(100而非50 mg·kg⁻¹·d⁻¹)也未达到此效果。长期持续应用降低剂量(25 mg·kg⁻¹·d⁻¹)并不能防止肌肉萎缩,反而会额外延迟萎缩进程。6. 得出的结论是,组织不相容的成肌细胞具有高度免疫原性,免疫排斥会导致巨大且永久性的肌肉缺陷,表明宿主肌肉组织被清除。初始短暂的免疫抑制可保护不相容细胞,但撤药后,会出现长期的免疫排斥反应和延迟的肌肉萎缩。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/33f22a9108ba/jphysiol00323-0231-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/32b970f5e906/jphysiol00323-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/1d65fbe78153/jphysiol00323-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/86ea5eaafafd/jphysiol00323-0229-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/1e8f07a849e3/jphysiol00323-0230-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/b41feffff184/jphysiol00323-0231-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/33f22a9108ba/jphysiol00323-0231-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/32b970f5e906/jphysiol00323-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/1d65fbe78153/jphysiol00323-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/86ea5eaafafd/jphysiol00323-0229-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/1e8f07a849e3/jphysiol00323-0230-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/b41feffff184/jphysiol00323-0231-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d007/1157910/33f22a9108ba/jphysiol00323-0231-b.jpg

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