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糖尿病免疫功能低下小鼠皮肤创伤的发展及牙髓干细胞产品用于愈合的研究。

Development of Cutaneous Wound in Diabetic Immunocompromised Mice and Use of Dental Pulp-Derived Stem Cell Product for Healing.

机构信息

Department of Pharmaceutical Sciences, Jerry H. Hodge School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX, USA.

出版信息

Methods Mol Biol. 2021;2193:23-30. doi: 10.1007/978-1-0716-0845-6_3.

DOI:10.1007/978-1-0716-0845-6_3
PMID:32808255
Abstract

Chronic nonhealing wounds impact nearly 15% of Medicare beneficiaries (8.2 million) in the United States costing $28-$32 billion annually. Despite advancement in wound management, approximately 8% of diabetic Medicare beneficiaries have a foot ulcer and 1.8% will have an amputation. The development of a regenerative approach is warranted to save these before-mentioned amputations. To this extent, herein, we describe the detailed methods in generating a type 1 diabetes mellitus (T1DM) condition in immunocompromised mice, inducing cutaneous wound, and application of dental pulp stem cell-derived secretory products for therapeutic assessment. This model helps in evaluating the efficacy of stem cell-based therapy and helps with the investigation of involved mechanisms in impaired cutaneous wound healing caused by hyperglycemic stress due to type 1 diabetes.

摘要

慢性难愈性伤口影响了美国近 15%的医疗保险受益人(820 万人),每年花费 280 亿至 320 亿美元。尽管伤口管理取得了进展,但大约 8%的糖尿病医疗保险受益人有足部溃疡,1.8%的人将进行截肢。为了避免这些截肢,有必要采用再生方法。在这方面,我们在此描述了在免疫功能低下的小鼠中产生 1 型糖尿病(T1DM)的详细方法,诱导皮肤伤口,并应用牙髓干细胞衍生的分泌产物进行治疗评估。该模型有助于评估基于干细胞的治疗效果,并有助于研究由于 1 型糖尿病引起的高血糖应激导致的受损皮肤伤口愈合的相关机制。

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Methods Mol Biol. 2021;2193:23-30. doi: 10.1007/978-1-0716-0845-6_3.
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引用本文的文献

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[Research advances on the mechanism of oral mucosal stem cells in promoting wound healing].口腔黏膜干细胞促进伤口愈合机制的研究进展
Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2023 May 20;39(5):496-500. doi: 10.3760/cma.j.cn501225-20220730-00321.
2
Immunomodulatory Mechanism and Potential Application of Dental Pulp-Derived Stem Cells in Immune-Mediated Diseases.牙髓干细胞的免疫调节机制及其在免疫介导性疾病中的潜在应用。
Int J Mol Sci. 2023 Apr 29;24(9):8068. doi: 10.3390/ijms24098068.