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成熟脂肪细胞去分化来源的去分化脂肪(DFAT)细胞移植可改善大鼠尿道括约肌收缩力。

Transplantation of mature adipocyte-derived dedifferentiated fat (DFAT) cells improves urethral sphincter contractility in a rat model.

机构信息

Department of Urology, Division of Cell Regeneration and Transplantation, Nihon University School of Medicine, Tokyo, Japan.

出版信息

Int J Urol. 2011 Dec;18(12):827-34. doi: 10.1111/j.1442-2042.2011.02865.x. Epub 2011 Oct 12.

Abstract

OBJECTIVES

To examine the effects of mature adipocyte-derived dedifferentiated fat (DFAT) cell transplantation on urethral tissue regeneration and sphincter function.

METHODS

Sixteen female Sprague-Dawley rats underwent vaginal distension (VD) for 3 h. Subsequently, green fluorescence protein (GFP)-labeled DFAT cells (1×10(6) in 20 µL saline, DFAT group, n=8) or saline (20 µL, control group, n=8) were injected into paraurethral connective tissue. Two weeks following VD, leak point pressure (LPP) was measured and an immunohistochemical analysis of the urethra was performed to evaluate urethral sphincter regeneration.

RESULTS

The VD model was characterized by atrophy of the urethral sphincter and showed a decrease in LPP. DFAT cell transplantation resulted in a significant improvement of LPP (DFAT group: 37.3±6.4 vs control group: 21.7±5.7 mmHg, P<0.01). Immunohistochemistry revealed that the striated muscle thickness and smooth muscle α-actin-positive area were significantly (P<0.05) larger in the DFAT group than in the control group. DFAT cell transplantation enhanced macrophage accumulation followed by an increased number of cells in the proliferative state. Transplanted DFAT cells were observed in the damaged smooth muscle layer and showed positive staining for smooth muscle α-actin, suggesting conversion into the smooth muscle cell phenotype.

CONCLUSIONS

DFAT cell transplantation promotes sphincter muscle regeneration and improves LPP in the rat VD model.

摘要

目的

研究成熟脂肪细胞去分化脂肪(DFAT)细胞移植对尿道组织再生和括约肌功能的影响。

方法

16 只雌性 Sprague-Dawley 大鼠行阴道扩张(VD)3 h。随后,将 GFP 标记的 DFAT 细胞(1×10(6)个细胞/20 µL 生理盐水,DFAT 组,n=8)或生理盐水(20 µL,对照组,n=8)注入尿道旁结缔组织。VD 后 2 周,测量漏点压(LPP),并对尿道进行免疫组织化学分析,以评估尿道括约肌再生。

结果

VD 模型表现为尿道括约肌萎缩,LPP 降低。DFAT 细胞移植可显著提高 LPP(DFAT 组:37.3±6.4 vs 对照组:21.7±5.7 mmHg,P<0.01)。免疫组织化学显示,DFAT 组的横纹肌厚度和平滑肌α-肌动蛋白阳性面积明显大于对照组(P<0.05)。DFAT 细胞移植促进了巨噬细胞的聚集,随后增殖状态的细胞数量增加。移植的 DFAT 细胞在受损的平滑肌层中被观察到,并显示出平滑肌α-肌动蛋白的阳性染色,表明其转化为平滑肌细胞表型。

结论

DFAT 细胞移植可促进尿道括约肌再生,提高大鼠 VD 模型的 LPP。

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