Ramirez Horacio A, Liang Liang, Pastar Irena, Rosa Ashley M, Stojadinovic Olivera, Zwick Thomas G, Kirsner Robert S, Maione Anna G, Garlick Jonathan A, Tomic-Canic Marjana
Human Genetics and Genomics Graduate Program in Biomedical Sciences, University of Miami Miller School of Medicine, Miami, FL, United States of America; Wound Healing and Regenerative Medicine Research Program, Department of Dermatology and Cutaneous Surgery, University of Miami Miller School Of Medicine, Miami, FL, United States of America.
Wound Healing and Regenerative Medicine Research Program, Department of Dermatology and Cutaneous Surgery, University of Miami Miller School Of Medicine, Miami, FL, United States of America.
PLoS One. 2015 Aug 28;10(8):e0137133. doi: 10.1371/journal.pone.0137133. eCollection 2015.
Diabetes Mellitus (DM) is a chronic, severe disease rapidly increasing in incidence and prevalence and is associated with numerous complications. Patients with DM are at high risk of developing diabetic foot ulcers (DFU) that often lead to lower limb amputations, long term disability, and a shortened lifespan. Despite this, the effects of DM on human foot skin biology are largely unknown. Thus, the focus of this study was to determine whether DM changes foot skin biology predisposing it for healing impairment and development of DFU. Foot skin samples were collected from 20 patients receiving corrective foot surgery and, using a combination of multiple molecular and cellular approaches, we performed comparative analyses of non-ulcerated non-neuropathic diabetic foot skin (DFS) and healthy non-diabetic foot skin (NFS). MicroRNA (miR) profiling of laser captured epidermis and primary dermal fibroblasts from both DFS and NFS samples identified 5 miRs de-regulated in the epidermis of DFS though none reached statistical significance. MiR-31-5p and miR-31-3p were most profoundly induced. Although none were significantly regulated in diabetic fibroblasts, miR-29c-3p showed a trend of up-regulation, which was confirmed by qPCR in a prospective set of 20 skin samples. Gene expression profiling of full thickness biopsies identified 36 de-regulated genes in DFS (>2 fold-change, unadjusted p-value ≤ 0.05). Of this group, three out of seven tested genes were confirmed by qPCR: SERPINB3 was up-regulated whereas OR2A4 and LGR5 were down-regulated in DFS. However no morphological differences in histology, collagen deposition, and number of blood vessels or lymphocytes were found. No difference in proliferative capacity was observed by quantification of Ki67 positive cells in epidermis. These findings suggest DM causes only subtle changes to foot skin. Since morphology, mRNA and miR levels were not affected in a major way, additional factors, such as neuropathy, vascular complications, or duration of DM, may further compromise tissue's healing ability leading to development of DFUs.
糖尿病(DM)是一种慢性、严重的疾病,其发病率和患病率正在迅速上升,且与多种并发症相关。糖尿病患者发生糖尿病足溃疡(DFU)的风险很高,DFU常导致下肢截肢、长期残疾和寿命缩短。尽管如此,糖尿病对人足部皮肤生物学的影响在很大程度上仍不清楚。因此,本研究的重点是确定糖尿病是否会改变足部皮肤生物学,使其易于出现愈合障碍和DFU的发生。从20名接受足部矫正手术的患者身上采集足部皮肤样本,并使用多种分子和细胞方法相结合,我们对未溃疡的非神经性糖尿病足部皮肤(DFS)和健康的非糖尿病足部皮肤(NFS)进行了比较分析。对DFS和NFS样本的激光捕获表皮和原代真皮成纤维细胞进行微小RNA(miR)分析,发现DFS表皮中有5种miR失调,尽管没有一种达到统计学意义。MiR-31-5p和miR-31-3p的诱导最为明显。虽然在糖尿病成纤维细胞中没有一种miR受到显著调节,但miR-29c-3p显示出上调趋势,这在前瞻性收集的20个皮肤样本中通过qPCR得到了证实。全层活检的基因表达谱分析确定DFS中有36个失调基因(变化倍数>2,未校正p值≤0.05)。在这一组中,7个测试基因中有3个通过qPCR得到证实:SERPINB3在DFS中上调,而OR2A4和LGR5在DFS中下调。然而,在组织学、胶原蛋白沉积、血管或淋巴细胞数量方面未发现形态学差异。通过对表皮中Ki67阳性细胞的定量分析,未观察到增殖能力的差异。这些发现表明糖尿病仅导致足部皮肤细微变化。由于形态、mRNA和miR水平未受到重大影响,其他因素,如神经病变、血管并发症或糖尿病病程,可能会进一步损害组织的愈合能力,导致DFU的发生。