Moskalenko Vasiliy, Ulrichs Karin, Kerscher Andreas, Blind Eberhard, Otto Christoph, Hamelmann Wulf, Demidchik Yurij, Timm Stephan
Department of Surgery I, Centre of Operative Medicine, University of Wuerzburg, Wuerzburg, Germany.
Transpl Int. 2007 Aug;20(8):688-96. doi: 10.1111/j.1432-2277.2007.00496.x. Epub 2007 May 19.
Allotransplantation of microencapsulated parathyroid tissue is a promising approach to the treatment of permanent hypoparathyroidism. Preoperative assessment of the quality of microencapsulated parathyroid tissue could facilitate selection of the optimal bioartifical graft for human parathyroid allotransplantation. Parathyroid tissue from patients with secondary hyperparathyroidism (n = 15) was processed mechanically or enzymatically (collagenase type II). Tissue particles and single cells/cell clusters were routinely microencapsulated with amitogenic Ba(2+) alginate. Parathyroid secretion dynamics in response to stimulation of nonencapsulated and microencapsulated parathyroid tissue with Ca(2+) were evaluated in a perifusion system. The stability of the different types of microcapsule was assessed using an osmotic pressure test. Mechanical cutting of parathyroid tissue led to peripheral necrosis of tissue particles and impaired their vitality. Collagenase digestion, in contrast, resulted in single cells and cell clusters without peripheral necrosis. The quality of microencapsulation of single cells/cell clusters was significantly better than that of tissue particles (deformed and imperfect capsules). Microencapsulation itself did not decrease cell vitality. Nonencapsulated and microencapsulated tissue particles and single cells/cell clusters from different donors maintained their own levels of response to stimulation with low Ca(2+). Microcapsules containing tissue particles showed poor stability compared with those containing single cells/cell clusters. Preoperative evaluation of microencapsulated parathyroid tissue can disclose differences in vitality and function and thus facilitate selection of the optimal bioartifical graft for human parathyroid allotransplantation.
微囊化甲状旁腺组织的同种异体移植是治疗永久性甲状旁腺功能减退症的一种有前景的方法。术前评估微囊化甲状旁腺组织的质量有助于为人类甲状旁腺同种异体移植选择最佳的生物人工移植物。对15例继发性甲状旁腺功能亢进患者的甲状旁腺组织进行机械或酶(II型胶原酶)处理。将组织颗粒和单细胞/细胞团常规用无致有丝分裂作用的钡离子藻酸盐进行微囊化。在灌流系统中评估未微囊化和微囊化甲状旁腺组织对钙离子刺激的甲状旁腺分泌动力学。使用渗透压测试评估不同类型微囊的稳定性。甲状旁腺组织的机械切割导致组织颗粒的周边坏死并损害其活力。相比之下,胶原酶消化产生的是没有周边坏死的单细胞和细胞团。单细胞/细胞团的微囊化质量明显优于组织颗粒(微囊变形且不完美)。微囊化本身并未降低细胞活力。来自不同供体的未微囊化和微囊化组织颗粒以及单细胞/细胞团维持其自身对低钙离子刺激的反应水平。与含有单细胞/细胞团的微囊相比,含有组织颗粒的微囊稳定性较差。术前评估微囊化甲状旁腺组织可以揭示活力和功能的差异,从而有助于为人类甲状旁腺同种异体移植选择最佳的生物人工移植物。