Division of Gastroenterology, Department of Medicine, Cedars Sinai Medical Center, Los Angeles, California, USA.
Developmental Biology and Regenerative Medicine Program, Saban Research Institute, Division of Pediatric Surgery, Children's Hospital Los Angeles, Keck School of Medicine, University of Southern California, Los Angeles California, USA.
Stem Cells Transl Med. 2017 Jan;6(1):238-248. doi: 10.5966/sctm.2016-0205. Epub 2016 Aug 30.
Liver disease affects large numbers of patients, yet there are limited treatments available to replace absent or ineffective cellular function of this crucial organ. Donor scarcity and the necessity for immunosuppression limit one effective therapy, orthotopic liver transplantation. But in some conditions such as inborn errors of metabolism or transient states of liver insufficiency, patients may be salvaged by providing partial quantities of functional liver tissue. After transplanting multicellular liver organoid units composed of a heterogeneous cellular population that includes adult stem and progenitor cells, both mouse and human tissue-engineered liver (TELi) form in vivo. TELi contains normal liver components such as hepatocytes with albumin expression, CK19-expressing bile ducts and vascular structures with α-smooth muscle actin expression, desmin-expressing stellate cells, and CD31-expressing endothelial cells. At 4 weeks, TELi contains proliferating albumin-expressing cells and identification of β2-microglobulin-expressing cells demonstrates that the majority of human TELi is composed of transplanted human cells. Human albumin is detected in the host mouse serum, indicating in vivo secretory function. Liquid chromatography/mass spectrometric analysis of mouse serum after debrisoquine administration is followed by a significant increase in the level of the human metabolite, 4-OH-debrisoquine, which supports the metabolic and xenobiotic capability of human TELi in vivo. Implanted TELi grew in a mouse model of inducible liver failure. Stem Cells Translational Medicine 2017;6:238-248.
肝脏疾病影响大量患者,但目前可用的治疗方法有限,无法替代这种关键器官缺失或无效的细胞功能。供体短缺和免疫抑制的必要性限制了一种有效的治疗方法,即原位肝移植。但在某些情况下,如先天性代谢错误或短暂的肝功能不全,患者可以通过提供部分功能正常的肝组织来挽救。在移植由包括成体干细胞和祖细胞在内的异质细胞群组成的多细胞肝类器官单位后,无论是小鼠还是人类组织工程化肝脏(TELi)都能在体内形成。TELi 包含正常的肝脏成分,如表达白蛋白的肝细胞、表达 CK19 的胆管以及表达α-平滑肌肌动蛋白的血管结构、表达 desmin 的星状细胞和表达 CD31 的内皮细胞。在第 4 周时,TELi 中含有增殖的表达白蛋白的细胞,并且鉴定出表达β2-微球蛋白的细胞表明,大多数人类 TELi 是由移植的人类细胞组成的。人白蛋白在宿主小鼠血清中被检测到,表明其具有体内分泌功能。对去莠敏给药后的小鼠血清进行液相色谱/质谱分析后,人类代谢产物 4-OH-去莠敏的水平显著增加,这支持了人类 TELi 在体内的代谢和外来化合物的能力。植入的 TELi 在诱导性肝衰竭的小鼠模型中生长。《干细胞转化医学》2017 年;6:238-248。