Daidzein Prevents the Increase in CD4+CD28null T Cells and B Lymphopoesis in Ovariectomized Mice: A Key Mechanism for Anti-Osteoclastogenic Effect

Estrogen deficiency leads to an upregulation of TNF-α producing T cells and B-lymphopoesis which augments osteoclastogenesis. Estrogen deficiency also increases the population of premature senescent CD4+CD28null T cells which secrete a higher amount of TNF-α thus leading to enhanced osteoclastogenesis. Isoflavonoids like daidzein and genistein are found mostly in soybeans, legumes, and peas. These share structural similarity with 17β-stradiol (E2) and have osteoprotective role. This study explores the effect of daidzein (Daid) on the proliferation of TNF-α producing T cells, premature senescent T cells and B cell lymphopoesis under estrogen deficient conditions. For this study adult Balb/c mice were treated with Daid at 10 mg/kg body weight dose by oral gavage daily post ovariectomy (Ovx). After six weeks animals were autopsied and bone marrow and spleen cells were collected for FACS analysis. Blood serum was collected for ELISA. It was observed that Ovx mice treated with Daid for six weeks show reduction in Ovx induced expansion of CD4+ T cells in bone marrow and spleen when analysed by flow cytometry. Estrogen deficiency led to increased prevalence of TNF-α secreting CD4+CD28null T cells, however, treatment with Daid increased the percentage of CD4+CD28+ T cells. Co-culture of CD4+CD28null T cells and bone marrow resulted in enhanced osteoclastogenesis as evident by increased tartarate resistant acid phosphatase (TRAP) expression, an osteoclast marker. However, treatment with Daid resulted in reduced osteoclastogenesis in CD4+CD28null T cells and bone marrow cell co-culture. Daid also regulated B lymphopoesis and decreased mRNA levels of RANKL in B220+ cells. Taken together, we propose that one of the mechanisms by which Daid prevents bone loss is by reversing the detrimental immune changes as a result of estrogen deficiency

Daid treatment inhibits Ovx-induced oxidative stress in CD4⁺ T cells and TNF-α production by these cells.

<p>(A) Cellular ROS measurement was performed by incubating CD4⁺ T cells with DCF-DA followed by FACS analysis. (B) Circulating TNF-α levels were measured in various groups by ELISA. (C) TNF-α mRNA levels in the BM CD4⁺ T cells were measured in various groups by qPCR. N = 10 mice/group; data are presented as mean ± SEM; ^**<i>P</i><0.01 and ^***<i>P</i><0.001 compared with Ovx+vehicle group.</p

Sequences of real-time PCR primers.

<p>Sequences of real-time PCR primers.</p

Thymus and spleen weight in Balb/c mice.

<p>Daid treatment decreases Ovx-induced increase in thymus and spleen weight. N = 10 mice/group). Data are presented as mean ± SEM;</p><p>***<i>P</i><0.001 compared with Ovx+vehicle group.</p

Daid treatment significantly decreased Ovx-induced increases in CD4⁺ T cell subsets in the BM and spleen.

<p>(A) CD4⁺ T cells in BM and (B) CD4⁺ T cells in spleen were quantified by flow cytometry as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0021216#s4" target="_blank">Materials and Methods</a>. N = 10 mice/group; data are presented as mean ± SEM; ^***<i>P</i><0.001 compared with Ovx+vehicle group.</p

Daid treatment significantly decreased Ovx-induced increases in B220⁺ cells in BM.

<p>(A and B) B220⁺ cells in BM were quantified by flow cytometry as described in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0021216#s4" target="_blank">Materials and Methods</a>. (C) OPG mRNA levels in the BM B220⁺ cells were measured in various groups by qPCR. (D) RANKL mRNA levels in the BM B220⁺ cells were measured in various groups by qPCR. N = 10 mice/group; data are presented as mean ± SEM; ^*<i>P</i><0.05, ^**<i>P</i><0.01, ^***<i>P</i><0.001 compared with Ovx+vehicle group.</p

Daidzein inhibits increased osteoclastogenesis in co-culture of bone marrow cells and TNF-α secreting CD4⁺CD28null T cells.

<p>(A) TRAP mRNA expression by qPCR in co-culture of BM cells and CD4⁺CD28null T cells. N = 3 mice/group; data are presented as mean ± SEM; ^***<i>P</i><0.001 compared with untreated co-culture of CD4⁺CD28null T cells with BM cells. (B) TNF-α levels were measured in the co-culture by ELISA. N = 3 mice/group; data are presented as mean ± SEM; ^***<i>P</i><0.001 compared with untreated co-culture of CD4⁺CD28null T cells with BM cells.</p