Deficiency of glucocorticoid receptor in bone marrow adipocytes has mild effects on bone and hematopoiesis but does not influence expansion of marrow adiposity with caloric restriction

Front Endocrinol (Lausanne). 2024 Jun 3:15:1397081. doi: 10.3389/fendo.2024.1397081. eCollection 2024.

Abstract

Introduction: Unlike white adipose tissue depots, bone marrow adipose tissue (BMAT) expands during caloric restriction (CR). Although mechanisms for BMAT expansion remain unclear, prior research suggested an intermediary role for increased circulating glucocorticoids.

Methods: In this study, we utilized a recently described mouse model (BMAd-Cre) to exclusively target bone marrow adipocytes (BMAds) for elimination of the glucocorticoid receptor (GR) (i.e. Nr3c1) whilst maintaining GR expression in other adipose depots.

Results: Mice lacking GR in BMAds (BMAd-Nr3c1 -/-) and control mice (BMAd-Nr3c1 +/+) were fed ad libitum or placed on a 30% CR diet for six weeks. On a normal chow diet, tibiae of female BMAd-Nr3c1-/- mice had slightly elevated proximal trabecular metaphyseal bone volume fraction and thickness. Both control and BMAd-Nr3c1-/- mice had increased circulating glucocorticoids and elevated numbers of BMAds in the proximal tibia following CR. However, no significant differences in trabecular and cortical bone were observed, and quantification with osmium tetroxide and μCT revealed no difference in BMAT accumulation between control or BMAd-Nr3c1 -/- mice. Differences in BMAd size were not observed between BMAd-Nr3c1-/- and control mice. Interestingly, BMAd-Nr3c1-/- mice had decreased circulating white blood cell counts 4 h into the light cycle.

Discussion: In conclusion, our data suggest that eliminating GR from BMAd has minor effects on bone and hematopoiesis, and does not impair BMAT accumulation during CR.

Keywords: bone; bone marrow adipose tissue (BMAT); caloric restriction (CR); glucocorticoid receptor (GR); glucocorticoids (GC); hematopoiesis.

MeSH terms

  • Adipocytes* / metabolism
  • Adipose Tissue / metabolism
  • Adiposity* / physiology
  • Animals
  • Bone Marrow* / metabolism
  • Bone and Bones / metabolism
  • Caloric Restriction*
  • Female
  • Hematopoiesis*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Glucocorticoid* / deficiency
  • Receptors, Glucocorticoid* / genetics
  • Receptors, Glucocorticoid* / metabolism

Substances

  • NR3C1 protein, mouse
  • Receptors, Glucocorticoid

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. The work was supported by grants from the NIH to OAM (AG069795; DK121759, DK137798), RLS (T32 DK101357; F32 DK123887), KTL (T32 DK071212, F32 DK122654), JNM (T32 HD007505, F31 DK135181) and by a grant from the American Diabetes Association to ZL (1-18-PDF-087).