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FK506 对大鼠股骨骨干、临界尺寸缺损愈合的影响。

Effects of FK506 on the healing of diaphyseal, critical size defects in the rat femur.

机构信息

Mayo Clinic, 200 First Street SW, Rochester, MN, 55905,

出版信息

Eur Cell Mater. 2020 Oct 6;40:160-171. doi: 10.22203/eCM.v040a10.

DOI:10.22203/eCM.v040a10
PMID:33021330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7816824/
Abstract

There is much interest in understanding the influence of the immune system on bone healing, including a number of reports suggesting a beneficial effect of FK506 (tacrolimus) in this regard. The influence of FK506 in a rat, femoral, critical size defect was examined using locally implanted, recombinant, human (rh) BMP-2 and adenovirally-transduced, autologous, adipose-derived mesenchymal stromal cells (AD-MSCs) expressing BMP-2. FK506 was delivered systemically using an implanted osmotic pump. Empty defects and those implanted with unmodified AD-MSCs did not heal in the presence or absence of FK506. Defects treated with rhBMP-2 healed with a large callus containing thin cortices and wispy trabeculae; this, too, was unaffected by FK506. A third of defects implanted with adenovirally-transduced AD-MSCs healed, but this improved to 100 % in the presence of FK506. New bone formed in response to BMP-2 synthesised endogenously by the genetically modified cells had a slimmer callus than those healed by rhBMP-2, with improved cortication and advanced reconstitution of marrow. These results suggest that FK506 may have had little effect on the intrinsic biology of bone healing, but improved healing in response to adenovirally-transduced cells by inhibiting immune responses to the first-generation adenovirus used here. Because the genetically modified cells produced bone of higher quality at far lower doses of BMP-2, this approach should be explored in subsequent research.

摘要

人们对了解免疫系统对骨骼愈合的影响很感兴趣,包括一些报告表明 FK506(他克莫司)在这方面具有有益作用。本研究通过局部植入重组人(rh)BMP-2 和腺病毒转导的、表达 BMP-2 的自体脂肪间充质基质细胞(AD-MSCs),研究了 FK506 在大鼠股骨临界尺寸缺损模型中的影响。通过植入的渗透泵系统给予 FK506。在存在或不存在 FK506 的情况下,未用 FK506 处理的空缺陷和未用未修饰的 AD-MSCs 处理的缺陷均未愈合。用 rhBMP-2 治疗的缺陷愈合良好,形成含有薄皮质和稀疏小梁的大骨痂;这也不受 FK506 的影响。用腺病毒转导的 AD-MSCs 植入的三分之一缺陷愈合,但在存在 FK506 的情况下,愈合率提高到 100%。内源性合成 BMP-2 的基因修饰细胞引起的新骨形成的骨痂比 rhBMP-2 治疗的骨痂更薄,皮质化更好,骨髓重建更先进。这些结果表明,FK506 可能对骨骼愈合的内在生物学几乎没有影响,但通过抑制对这里使用的第一代腺病毒的免疫反应,改善了对腺病毒转导细胞的愈合。因为基因修饰细胞在使用更低剂量的 BMP-2 时产生了更高质量的骨,因此应该在后续研究中探索这种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/3172530cc1e7/nihms-1660254-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/0661d4c979f2/nihms-1660254-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/c0903545e94e/nihms-1660254-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/380ec7a54514/nihms-1660254-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/bf88b4a39a22/nihms-1660254-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/3172530cc1e7/nihms-1660254-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/0661d4c979f2/nihms-1660254-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/c0903545e94e/nihms-1660254-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/380ec7a54514/nihms-1660254-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/bf88b4a39a22/nihms-1660254-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f84c/7816824/3172530cc1e7/nihms-1660254-f0005.jpg

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