<p>(<b>A</b>) WAT derived from wild-type (wt) and obese ob<i>/</i>ob mice was subjected to qRT-PCR. Increased gene expression of CD68, MCP-1, furin, MT1-MMP, and PCSK5 was found in ob<i>/</i>ob mice (*p<0.05; **p<0.01 vs. wt). (<b>B</b>) Supernatants from WAT cultures of ob<i>/</i>ob mice increased THP-1/ϕ migration (<sup>##</sup>p<0.05 vs. wt), comparable to MCP-1 (*p<0.05 vs. control, co.; **p<0.01 vs. 50 ng/mL MCP-1). (<b>C</b>) Supernatant-facilitated migration was inhibited by dec-CMK (CMK, 50 µmol/L; 12h) or the MMP-inhibitor GM6001 (50 µmol/L; 12h) (both #p<0.05 vs. controls, co.). n=3.</p
High phenotypic variation in diet-induced obesity in male C57BL/6J inbred mice suggests a molecular ...
OBJECTIVE—To establish the mechanism of the phenotypic switch of adipose tissue macrophages (ATMs) f...
<p>qRT-PCR quantification of CXCL2 (a), CCL5 (b), leptin (c) and FABP4 (d) mRNA expression in subcut...
<p><b>A.</b> Representative flow diagram (top) and quantification (bottom) of migrated DCs (MHCII<su...
Adipose tissue macrophages (ATMs) infiltrate adipose tissue during obesity and contribute to insulin...
Tissue-resident macrophages in white adipose tissue (WAT) dynamically adapt to the metabolic changes...
Adipose tissue macrophages (ATMs) present in the epididymal white adipose tissue (EWAT) are separate...
<p>Retroperirenal adipose tissue mRNA expressions of F4/80 (total macrophage, A), CD11c (type M1, B)...
<p>Levels of pro-inflammatory (a) TNFα and (b) IL-1β secretion into media from adipose tissue explan...
We previously demonstrated a marked upregulation in the bone morphogenic protein (BMP)/growth differ...
<p>(a) Immunoblot analysis of MIF and control β-actin in adipose of lean and obese WT mice (n = 4). ...
Adipose tissue macrophages (ATMs) regulate homeostasis and contribute to the metabolically harmful c...
<p>MAP3K8-ko and WT mice were fed a LFD or HFD during 16 weeks. (a) Bodyweight development upon LFD ...
AbstractWe previously demonstrated a marked upregulation in the bone morphogenic protein (BMP)/growt...
The mRNA levels for the mitochondrial uncoupling protein (UCP1) in fat tissues of A/J and C57BL/6J i...
High phenotypic variation in diet-induced obesity in male C57BL/6J inbred mice suggests a molecular ...
OBJECTIVE—To establish the mechanism of the phenotypic switch of adipose tissue macrophages (ATMs) f...
<p>qRT-PCR quantification of CXCL2 (a), CCL5 (b), leptin (c) and FABP4 (d) mRNA expression in subcut...
<p><b>A.</b> Representative flow diagram (top) and quantification (bottom) of migrated DCs (MHCII<su...
Adipose tissue macrophages (ATMs) infiltrate adipose tissue during obesity and contribute to insulin...
Tissue-resident macrophages in white adipose tissue (WAT) dynamically adapt to the metabolic changes...
Adipose tissue macrophages (ATMs) present in the epididymal white adipose tissue (EWAT) are separate...
<p>Retroperirenal adipose tissue mRNA expressions of F4/80 (total macrophage, A), CD11c (type M1, B)...
<p>Levels of pro-inflammatory (a) TNFα and (b) IL-1β secretion into media from adipose tissue explan...
We previously demonstrated a marked upregulation in the bone morphogenic protein (BMP)/growth differ...
<p>(a) Immunoblot analysis of MIF and control β-actin in adipose of lean and obese WT mice (n = 4). ...
Adipose tissue macrophages (ATMs) regulate homeostasis and contribute to the metabolically harmful c...
<p>MAP3K8-ko and WT mice were fed a LFD or HFD during 16 weeks. (a) Bodyweight development upon LFD ...
AbstractWe previously demonstrated a marked upregulation in the bone morphogenic protein (BMP)/growt...
The mRNA levels for the mitochondrial uncoupling protein (UCP1) in fat tissues of A/J and C57BL/6J i...
High phenotypic variation in diet-induced obesity in male C57BL/6J inbred mice suggests a molecular ...
OBJECTIVE—To establish the mechanism of the phenotypic switch of adipose tissue macrophages (ATMs) f...
<p>qRT-PCR quantification of CXCL2 (a), CCL5 (b), leptin (c) and FABP4 (d) mRNA expression in subcut...