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Cell‐mediated mineralization in culture at low temperature associated with subtle thermogenic response
Author(s) -
Klein Benjamin Y.,
Gal I.,
BenBassat H.
Publication year - 1996
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/(sici)1097-4644(19961101)63:2<229::aid-jcb10>3.0.co;2-e
Subject(s) - mineralization (soil science) , incubation , stromal cell , oxidative phosphorylation , chemistry , medicine , endocrinology , biophysics , cell culture , intracellular , metabolism , biochemistry , biology , microbiology and biotechnology , organic chemistry , nitrogen , genetics
In both the growth plate and in marrow stromal cell cultures cell‐mediated mineralization is preceded by characteristics of anaerobic and low efficiency energy metabolism. Reagents that increase mineralization like malonate and dexamethasone (DEX) also increase the mitochondrial membrane potential (MtMP) especially 1 week after DEX stimulation. Contrarily, levamisole, which decreases mineralization, also decreases MtMP. Modulation of MtMP and energy metabolism could be linked to regulation of mineralization by the uncoupling of oxidative phosphorylation. This uncoupling should be associated with thermogenesis in cells that induce mineralization. We examined whether cold temperature affects mineralization, and whether cellular thermogenesis takes place at cold temperature in parallel to changes in MtMP. Osteoprogenitor cells (OPC) induced, in DEX stimulated rat marrow stroma, higher mineralization at 33°C than at 37°C. Increased mineralization by cold temperature required long incubation since incubation in the cold during short intervals, 3–4 days, did not increase mineralization relative to (37°C) controls. Marrow stromal cells in the presence of valinomycin responded to incubation at 33°C by retaining all the vital dye after 4 h, unlike the cells at 37°C; however, after 24 h the level of dye retention at 33°C was the same as at 37°C. The delayed response of the temperature‐dependent (> 37°C) K + ionophor to incubation in the cold indicated that certain cells may respond to low temperature by local intracellular heating, and by heat conduction to the plasma membrane. DEX‐stimulated stromal cells, unlike unstimulated cells, showed increased mitochondrial rhodamine 123 retention in the presence of valinomycin after 24 h in the cold, which corresponds to day 4 of OPC induction. This is consistent with the concept that valinomycin‐induced cell damage is mediated by (cold‐induced) local heating. The mechanism of this cell damage should selectively prefer non‐thermogenic (rhodamine retaining) over thermogenic (rhodamine leaking) cells such as OPC. At cold temperature DEX‐stimulated stromal cells showed the best anti‐OPC selection under exposure to valinomycine between days 3–7, concurrent with the period of rhodamine leakage from the mitochondria. These results indicate that thermogenesis is enhanced during the period of low MtMP in mineralizing cells, and prolonged exposure to cold increases mineralization also due to induction of subtle thermogenesis. © 1996 Wiley‐Liss, Inc.