Sumi Shoichiro, Gu Yuanjun, Hiura Akihito, Inoue Kazutomo
Department of Organ Reconstruction, Institute for Frontier Medical Sciences, Kyoto University, Kyoto, Japan.
Pancreas. 2004 Oct;29(3):e85-9. doi: 10.1097/00006676-200410000-00017.
A profound knowledge of the development and differentiation of pancreatic tissues, especially islets of Langerhans, is necessary for developing regenerative therapy for severe diabetes mellitus. A recent developmental study showed that PTF-1a is expressed in almost all parts of pancreatic tissues, in addition to PDX-1, a well-known transcription factor that is essential for pancreas development. Another study suggested that alpha cells and beta cells individually, but not sequentially, differentiated from neurogenin-3--expressing precursor cells. Under strong induction of pancreas regeneration, it is likely that pancreatic duct cells dedifferentiate to grow, express PDX-1, and re-differentiate toward other cell types including islet cells. Duct epithelium-like cells can be cultivated from crude pancreatic exocrine cells and can be induced to differentiate toward islet-like cell clusters under some culture conditions. These cell clusters made from murine pancreas have been shown to control hyperglycemia when transplanted into diabetic mice. Liver-derived oval cells and their putative precursor H-CFU-C have been shown to differentiate toward pancreatic cells. Furthermore, extrapancreatic cells contained in bone marrow and amniotic membrane are reported to become insulin-producing cells. However, their exact characterization and relationship between these cell types remain to be elucidated. Our recent study has shown that islet-like cell clusters can be differentiated from mouse embryonic stem cells. Transplantation of these clusters could ameliorate hyperglycemia of STZ-induced diabetic mice without forming teratomas. Interestingly, these cells expressed several genes specific to exocrine pancreatic tissue in addition to islet-related genes, suggesting that stable and efficient differentiation toward certain tissues can only be achieved through a process mimicking normal development of the tissue. Perhaps recent developments in these fields may rapidly lead to an established regenerative therapy for diabetes mellitus.
深入了解胰腺组织,尤其是胰岛的发育和分化,对于开发重症糖尿病的再生疗法至关重要。最近的一项发育研究表明,除了PDX - 1(一种对胰腺发育至关重要的著名转录因子)外,PTF - 1a在胰腺组织的几乎所有部位均有表达。另一项研究表明,α细胞和β细胞分别而非顺序地从表达神经源蛋白 - 3的前体细胞分化而来。在胰腺再生的强烈诱导下,胰腺导管细胞很可能去分化以生长、表达PDX - 1,并重新分化为包括胰岛细胞在内的其他细胞类型。导管上皮样细胞可从粗制的胰腺外分泌细胞中培养出来,并在某些培养条件下被诱导分化为胰岛样细胞簇。已证明,将这些源自小鼠胰腺的细胞簇移植到糖尿病小鼠体内可控制高血糖。肝脏来源的卵圆细胞及其假定的前体H - CFU - C已被证明可向胰腺细胞分化。此外,据报道,骨髓和羊膜中含有的胰腺外细胞可成为产生胰岛素的细胞。然而,它们的确切特征以及这些细胞类型之间的关系仍有待阐明。我们最近的研究表明,胰岛样细胞簇可从小鼠胚胎干细胞分化而来。移植这些细胞簇可改善链脲佐菌素诱导的糖尿病小鼠的高血糖,且不会形成畸胎瘤。有趣的是,这些细胞除了表达与胰岛相关的基因外,还表达了几种胰腺外分泌组织特有的基因,这表明只有通过模拟组织正常发育的过程才能实现向特定组织的稳定而有效的分化。也许这些领域的最新进展可能会迅速促成一种成熟的糖尿病再生疗法。