Research Article

Monocytes Do Not Transdifferentiate into Proper Osteoblasts

Figure 1

Treatments to obtain PCMOs and MOMPs influence proliferation and expression of monocytes. (a) Human mononuclear cells ( 𝑁 = 4 , 𝑛 = 3 ) were cultivated without specific treatment (Mo), treated for 6 days to obtain MOMPs (M) or PCMOs (P). Viability was measured by Alamar blue assay on day 6. P shows a significantly higher viability than Mo (*** 𝑃 < 0 . 0 0 1 ). (b) Relative expression levels of CD34 measured by RT-PCR normalized to GAPDH and subsequently to expression of CD34 in nonadherent bone marrow cells (naBMCs) as internal control ( 𝑁 = 3 , 𝑛 = 3 ). Mo and M show a significantly higher expression of CD34 on day 6 than Mo on day 1 (** 𝑃 < 0 . 0 1 ; *** 𝑃 < 0 . 0 0 1 ). After osteogenic differentiation, CD34 levels in Mo decreased significantly in comparison to Mo on day 6 (°° 𝑃 < 0 . 0 5 ). (c) Relative expression levels of collagen type 1 measured by RT-PCR normalized to GAPDH and subsequently to expression of collagen type 1 in primary osteoblasts (O) as internal control ( 𝑁 = 3 , 𝑛 = 3 ). Mo, M and P show expression of low levels of collagen type 1 on all days (*** 𝑃 < 0 . 0 0 1 ). Monocytes (Mo) day 1: freshly isolated monocytes; Mo, MOMP (M), and PCMO (P) day 6: cells after treatment; Mo, M, P day 20: cells after differentiation with vitamin D containing medium.
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