Deshmukh K, Kline W G, Sawyer B D
Biochim Biophys Acta. 1977 Aug 25;499(1):28-35. doi: 10.1016/0304-4165(77)90225-2.
Rabbit articular chondrocytes in suspension culture synthesize Type II collagen [3alpha1(II)] in the absence of extracellular Ca2+ and Type I collagen [2alpha1(I) - alpha2] in the complete medium. As a result of pre-treatment in monolayer culture with calcitonin or parathyroid hormone in the complete medium, an influx of Ca2+ into the cells occurs. These cells produce mainly Type I collagen when transferred to suspension cultures in the medium devoid of CaCl2. If added directly to the suspension culture medium containing no CaCl2, calcitonin stimulates an active efflux of Ca2+ from the cells into the medium and leads the cells to synthesize Type I collagen. Under similar conditions, parathyroid hormone does not change the collagen-phenotype.
悬浮培养的兔关节软骨细胞在无细胞外Ca2+的情况下合成II型胶原[3α1(II)],在完全培养基中合成I型胶原[2α1(I)-α2]。在完全培养基中用降钙素或甲状旁腺激素进行单层培养预处理后,细胞会发生Ca2+内流。当将这些细胞转移到不含CaCl2的培养基中进行悬浮培养时,它们主要产生I型胶原。如果直接添加到不含CaCl2的悬浮培养基中,降钙素会刺激Ca2+从细胞中主动流出到培养基中,并导致细胞合成I型胶原。在类似条件下,甲状旁腺激素不会改变胶原表型。