Department of Chemistry, Purdue University, 720 Clinic Drive, West Lafayette, IN, 47907-2084, USA.
Inflamm Res. 2015 Sep;64(9):697-706. doi: 10.1007/s00011-015-0849-2. Epub 2015 Jul 7.
Adipose tissue macrophages (ATMs) have been implicated in a number of obesity-related diseases. Because the activated macrophages associated with many types of autoimmune and inflammatory diseases express a folate receptor (FR) that can be exploited for FR-targeted drug delivery, we examined the visceral adipose tissue of obese mice and humans to determine whether ATMs also express FR that are accessible by folate conjugates.
C57BL/6 or FATSO mice fed on either a low- or high-fat diet were used in murine studies. Human adipose tissue were obtained from healthy volunteers during adipose reduction surgery.
Visceral adipose tissue was collected from both obese mice and humans, collagenase digested, and stained with folate-Oregon Green and antibodies for macrophage markers including F4/80, mannose receptor (CD206), CD11b, and CD11c. Cells were then examined for expression of the above markers by flow cytometry. Furthermore, the ability of folate conjugates to target the FR-expressing ATMs in obese mice was evaluated in vivo.
A subset of the ATMs harvested from obese mice were found to express FR. Subpopulations of ATMs also simultaneously express both pro- and anti-inflammatory markers, and FR is expressed on both subsets. We then demonstrate that FR-expressing ATMs can be targeted with folate-linked fluorescent dyes in vivo.
FR are expressed on multiple subsets of ATMs and these subsets can be targeted with folate-linked drugs, allowing for the possible development of FR-targeted therapies for obesity-related inflammatory diseases.
脂肪组织巨噬细胞(ATMs)与许多肥胖相关疾病有关。由于与许多类型的自身免疫和炎症性疾病相关的激活巨噬细胞表达可用于 FR 靶向药物递送的叶酸受体(FR),我们检查了肥胖小鼠和人类的内脏脂肪组织,以确定 ATMs 是否也表达 FR,而 FR 可被叶酸缀合物靶向。
用低脂或高脂饮食喂养的 C57BL/6 或 FATSO 小鼠用于小鼠研究。人类脂肪组织是从健康志愿者在脂肪减少手术期间获得的。
从肥胖小鼠和人类中收集内脏脂肪组织,用胶原酶消化,并与叶酸-Oregon Green 和巨噬细胞标志物(包括 F4/80、甘露糖受体(CD206)、CD11b 和 CD11c)的抗体染色。然后通过流式细胞术检查上述标志物的表达。此外,还评估了叶酸缀合物在肥胖小鼠体内靶向 FR 表达的 ATMs 的能力。
从肥胖小鼠中分离出的 ATMs 中有一部分表达 FR。ATMs 的亚群也同时表达促炎和抗炎标志物,并且 FR 在这两个亚群上都表达。然后,我们证明 FR 表达的 ATMs 可以在体内用叶酸连接的荧光染料靶向。
FR 在多个 ATMs 亚群上表达,这些亚群可以用叶酸连接的药物靶向,从而为肥胖相关炎症性疾病的 FR 靶向治疗的发展提供了可能。