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缺乏细胞间黏附分子-1(ICAM-1)和巨噬细胞-1抗原(Mac-1)黏附受体的小鼠脂肪组织中的白细胞迁移

Leukocyte migration in adipose tissue of mice null for ICAM-1 and Mac-1 adhesion receptors.

作者信息

Robker Rebecca L, Collins Robert G, Beaudet Arthur L, Mersmann Harry J, Smith C Wayne

机构信息

Section of Leukocyte Biology, Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, 1100 Bates Avenue, Houston, TX 77030, USA.

出版信息

Obes Res. 2004 Jun;12(6):936-40. doi: 10.1038/oby.2004.114.

Abstract

OBJECTIVE

To determine whether the leukocyte adhesion receptors ICAM-1 and Mac-1, regulators of immune cell migration, have an intrinsic role within adipose tissue by 1) analyzing the expression of ICAM-1 in adipose tissue, 2) identifying leukocyte populations within adipose tissue, and 3) determining whether ICAM-1 and Mac-1 mutant mice exhibit abnormal numbers of adipose tissue leukocytes.

RESEARCH METHODS AND PROCEDURES

Wild-type, ICAM-1(-/-), and Mac-1(-/-) mice were fed a long-term high-fat diet. ICAM-1 expression was analyzed by Northern blot and immunohistochemistry. Leukocytes within adipose tissue were identified by immunohistochemistry and flow cytometry.

RESULTS

ICAM-1 was expressed in adipose tissue and localized to the vascular endothelium. Macrophages and lymphocytes were prevalent within the stromal-vascular cell fraction of adipose tissue, and gender-specific differences were observed, with adipose tissue from female mice containing significantly more macrophages than tissue from male mice. Numbers of leukocytes in ICAM-1(-/-) and Mac-1(-/-) mice were not different from wild-types, however, indicating that these adhesion receptors are not required for leukocyte migration into adipose tissue.

DISCUSSION

Our results documented leukocyte populations within adipose tissue, which may be involved in the development of heightened inflammation that is characteristic of obesity.

摘要

目的

通过以下方式确定白细胞黏附受体ICAM - 1和Mac - 1(免疫细胞迁移的调节因子)在脂肪组织中是否具有内在作用:1)分析ICAM - 1在脂肪组织中的表达;2)识别脂肪组织中的白细胞群体;3)确定ICAM - 1和Mac - 1突变小鼠的脂肪组织白细胞数量是否异常。

研究方法与步骤

对野生型、ICAM - 1基因敲除(- / -)和Mac - 1基因敲除(- / -)小鼠进行长期高脂饮食喂养。通过Northern印迹法和免疫组织化学分析ICAM - 1的表达。通过免疫组织化学和流式细胞术识别脂肪组织中的白细胞。

结果

ICAM - 1在脂肪组织中表达,并定位于血管内皮。巨噬细胞和淋巴细胞在脂肪组织的基质血管细胞部分中普遍存在,并且观察到性别特异性差异,雌性小鼠的脂肪组织中巨噬细胞明显多于雄性小鼠的组织。然而,ICAM - 1基因敲除(- / -)和Mac - 1基因敲除(- / -)小鼠的白细胞数量与野生型小鼠没有差异,这表明这些黏附受体不是白细胞迁移到脂肪组织所必需的。

讨论

我们的结果记录了脂肪组织中的白细胞群体,其可能参与肥胖特征性的炎症加剧的发展。

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