King Michael W, Neff Anton W, Mescher Anthony L
Indiana University Center for Regenerative Biology and Medicine, Indiana University School of Medicine-Terre Haute, 47809, USA.
Int J Dev Biol. 2009;53(7):955-69. doi: 10.1387/ijdb.082719mk.
During amphibian epimorphic limb regeneration, local injury produces metabolic changes that lead to cellular dedifferentiation and formation of a blastema, but few details of these changes have been elucidated. Here we report the first global proteomic analysis of epimorphic regeneration comparing the profiles of abundant proteins in larval limbs of the anuran Xenopus laevis (stage 53) at the time of amputation (0dPA) and 3 days post-amputation when the regeneration blastema is developing (3dPA). We identified and quantified 1517 peptides, of which 1067 were identified with high peptide ID confidence. Of these 1067 proteins, 489 showed significant changes in quantity between the two groups. Taking into account identical peptides whose fold changes were within 20%, and not including peptides whose fold changes were below the observed fold changes of peptides for the internal standard (chicken lysozyme), we were able to identify 145 peptides elevated in 3dPA relative to 0dPA and 220 peptides in 0dPA relative to 3dPA. In this report, we focus on those proteins that were elevated in the 3dPA tissue relative to 0dPA. In this class were members of the annexin family (e.g. ANXA1, ANXA2, ANXA5) and the ANXA2-binding partner S100A10, which have important immunoregulatory roles in other systems and were also shown to be differentially expressed in stage 53 and 57 3dPA and 5dPA blastemas in our previous microarray studies. Besides elucidating the possible modulation of inflammation during amphibian limb regeneration, our proteomic study also provides insight into dedifferentiation by revealing up-regulation of proteins known to characterize many stem cells.
在两栖动物肢体的再生过程中,局部损伤会引发代谢变化,从而导致细胞去分化并形成芽基,但这些变化的细节鲜有阐明。在此,我们报告了首次对两栖动物肢体再生进行的全蛋白质组分析,比较了无尾目非洲爪蟾(第53阶段)幼体肢体在截肢时(截肢后0天)和再生芽基正在发育时(截肢后3天)丰富蛋白质的谱图。我们鉴定并定量了1517个肽段,其中1067个肽段的肽段ID可信度较高。在这1067种蛋白质中,有489种在两组之间的数量上显示出显著变化。考虑到倍数变化在20%以内的相同肽段,且不包括倍数变化低于内标(鸡溶菌酶)肽段观察到的倍数变化的肽段,我们能够鉴定出相对于0天在3天中升高的145个肽段以及相对于3天在0天中升高的220个肽段。在本报告中,我们重点关注那些相对于0天在3天组织中升高的蛋白质。这一类包括膜联蛋白家族成员(如膜联蛋白A1、膜联蛋白A2、膜联蛋白A5)以及膜联蛋白A2结合伴侣S100A10,它们在其他系统中具有重要的免疫调节作用,并且在我们之前的微阵列研究中也显示在第53和57阶段的3天和5天再生芽基中差异表达。除了阐明两栖动物肢体再生过程中炎症可能的调节作用外,我们的蛋白质组研究还通过揭示已知表征许多干细胞的蛋白质的上调,为去分化提供了见解。