دورية أكاديمية

Matrix regulation of skeletal cell apoptosis. Role of calcium and phosphate ions

التفاصيل البيبلوغرافية
العنوان: Matrix regulation of skeletal cell apoptosis. Role of calcium and phosphate ions
المؤلفون: Adams, Christopher S., Mansfield, K., Perlot, R. L., Shapiro, I. M.
المصدر: PCOM Scholarly Papers
سنة النشر: 2001
المجموعة: Philadelphia College of Osteopathic Medicine: DigitalCommons@PCOM
مصطلحات موضوعية: Biological membranes, Bone, Calcium, Cells, Enzyme inhibition, Phosphates, Extracellular matrix, Biochemistry, calcium channel blocking agent, calcium ion, caspase 3, endonuclease, phosphate, apoptosis, article, cell membrane, cell viability, concentration response, controlled study, cytosol, enzyme activity, human, human cell, membrane potential, mitochondrial membrane, nick end labeling, osteoblast, osteolysis, priority journal, regulatory mechanism
الوصف: Previously, we noted that inorganic phosphate (Pi), a major component of bone extracellular matrix, induced osteoblast apoptosis (Meleti, Z., Shapiro, I. M., and Adams, C. S. (2000) Bone (NY) 27, 359-366). Since Ca2+ along with Pi is released from bone during the resorption process, we advanced the hypothesis that Ca2+ modulates Pi-mediated osteoblast apoptosis. To test this hypothesis, osteoblasts were incubated with both ions, and cell death was determined. We noted that a modest increase in the medium Ca2+ concentrations ([Ca2+]e) of 0.1-1 mm caused a profound and rapid enhancement in Pi-dependent death of cultured osteoblasts. An elevation in [Ca2+]e alone had no effect on osteoblast viability, whereas Ca2+ channel blockers failed to inhibit killing of ion pair-treated cells. These results indicated that Pi-mediated cell death is not dependent on a sustained increase in the cytosolic Ca 2+ concentration. Terminal dUTP nick-end labeling analysis and measurement of caspase-3 activity of the ion pair-treated cells suggested that death was apoptotic. Apoptosis was confirmed using caspase-3 and endonuclease inhibitors. The mitochondrial membrane potential and cytosolic Ca2+ status of the treated cells were evaluated. After incubation with [Ca 2+]e and Pi, a decrease in mitochondrial fluorescence was noted, suggesting that the ions decreased the mitochondrial transmembrane potential. Subsequent to the fall in mitochondrial membrane potential, there was a transient elevation in the cytosolic Ca2+ concentration. Results of the study suggest that the ion pair conspire at the level of the plasma membrane to induce intracellular changes that result in loss of mitochondrial function. The subsequent increase in the cytosolic Ca 2+ concentration may trigger downstream events that transduce osteoblast apoptosis.
نوع الوثيقة: text
اللغة: unknown
العلاقة: https://digitalcommons.pcom.edu/scholarly_papers/1547Test
الإتاحة: https://digitalcommons.pcom.edu/scholarly_papers/1547Test
رقم الانضمام: edsbas.38EB7BFD
قاعدة البيانات: BASE