Next Article in Journal
It Takes Two: Dimerization Is Essential for the Broad-Spectrum Predatory and Defensive Activities of the Venom Peptide Mp1a from the Jack Jumper Ant Myrmecia pilosula
Previous Article in Journal
Hyaluronan Metabolism is Associated with DNA Repair Genes in Breast and Colorectal Cancer. Screening of Potential Progression Markers Using qPCR

The Fabp4-Cre-Model is Insufficient to Study Hoxc9 Function in Adipose Tissue

Medical Department III—Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, D-04103 Leipzig, Germany
Institute of Anatomy, Leipzig University, D-04103 Leipzig, Germany
Institute of Anatomy and Cell Biology, Martin-Luther-University, D-06108 Halle (Saale), Germany
Helmholtz Institute for Metabolic, Obesity and Vascular Research (HI-MAG) of the Helmholtz Zentrum München at the University of Leipzig and University Hospital Leipzig, Leipzig University, D-04103 Leipzig, Germany
Authors to whom correspondence should be addressed.
Biomedicines 2020, 8(7), 184;
Received: 18 May 2020 / Revised: 18 June 2020 / Accepted: 26 June 2020 / Published: 29 June 2020
(This article belongs to the Section Model Systems in Research and Development)
Developmental genes are important regulators of fat distribution and adipose tissue (AT) function. In humans, the expression of homeobox c9 (HOXC9) is significantly higher in subcutaneous compared to omental AT and correlates with body fat mass. To gain more mechanistic insights into the role of Hoxc9 in AT, we generated Fabp4-Cre-mediated Hoxc9 knockout mice (ATHoxc9-/-). Male and female ATHoxc9-/- mice were studied together with littermate controls both under chow diet (CD) and high-fat diet (HFD) conditions. Under HFD, only male ATHoxc9-/- mice gained less body weight and exhibited improved glucose tolerance. In both male and female mice, body weight, as well as the parameters of glucose metabolism and AT function were not significantly different between ATHoxc9-/- and littermate control CD fed mice. We found that crossing Hoxc9 floxed mice with Fabp4-Cre mice did not produce a biologically relevant ablation of Hoxc9 in AT. However, we hypothesized that even subtle reductions of the generally low AT Hoxc9 expression may cause the leaner and metabolically healthier phenotype of male HFD-challenged ATHoxc9-/- mice. Different models of in vitro adipogenesis revealed that Hoxc9 expression precedes the expression of Fabp4, suggesting that ablation of Hoxc9 expression in AT needs to be achieved by targeting earlier stages of AT development. View Full-Text
Keywords: developmental genes; adipose tissue; obesity; adipocytes developmental genes; adipose tissue; obesity; adipocytes
Show Figures

Figure 1

MDPI and ACS Style

Dommel, S.; Berger, C.; Kunath, A.; Kern, M.; Gericke, M.; Kovacs, P.; Guiu-Jurado, E.; Klöting, N.; Blüher, M. The Fabp4-Cre-Model is Insufficient to Study Hoxc9 Function in Adipose Tissue. Biomedicines 2020, 8, 184.

AMA Style

Dommel S, Berger C, Kunath A, Kern M, Gericke M, Kovacs P, Guiu-Jurado E, Klöting N, Blüher M. The Fabp4-Cre-Model is Insufficient to Study Hoxc9 Function in Adipose Tissue. Biomedicines. 2020; 8(7):184.

Chicago/Turabian Style

Dommel, Sebastian; Berger, Claudia; Kunath, Anne; Kern, Matthias; Gericke, Martin; Kovacs, Peter; Guiu-Jurado, Esther; Klöting, Nora; Blüher, Matthias. 2020. "The Fabp4-Cre-Model is Insufficient to Study Hoxc9 Function in Adipose Tissue" Biomedicines 8, no. 7: 184.

Find Other Styles
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

Search more from Scilit
Back to TopTop