Murawala H, Patel S, Ranadive I, Desai I, Balakrishnan S
Department of Zoology, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, 390002, Gujarat, India.
N. V. Patel College of Pure and Applied Sciences, Vallabh Vidya Nagar, Anand, 388120, Gujarat, India.
J Fish Biol. 2018 May;92(5):1604-1619. doi: 10.1111/jfb.13618. Epub 2018 Apr 6.
Alteration in the expression pattern of matrix metalloproteinase (MMP)2 and MMP9 was studied in the regenerating caudal fin of Poecilia latipinna immediately following amputation until the new tissues gained structural integrity. Timed expression pattern of these two MMPs was studied at enzyme, transcript as well as protein levels. Additionally, both the gelatinases were localized in the regenerating caudal fin during three specific stages of regeneration. The results revealed a progressive increase in the expression of MMP2 starting at 1 h post amputation (hpa), indicating its possible role in the remodelling of extracellular matrix early on during caudal-fin regeneration. Nevertheless, a reduction in transcript level expression of MMP2 at 6 hpa and 12 hpa stages, points towards a possible transcriptional regulation, to further moderate its activity. As observed in the case of MMP2, expression of MMP9 too increased from 1 hpa and remained elevated until 5 dpa. However, the active MMP9 revealed its presence only 12 hpa onwards. Moreover, both the gelatinases were localised in the apical epithelial cap and in the progress zone at wound epithelium (1 dpa) and blastema (60 hpa) stages respectively. Further, during early differentiation stage (5 dpa), high intensities of MMP2 and MMP9 were localized in the newly formed actinotrichia as compared with the tissue proximal to it. Based on the results, it could be construed that the controlled up-regulation of MMP2 and MMP9 from 1 hpa until the early differentiation stage ensures a regulated digestion of extracellular matrix, perhaps to facilitate the recruitment, proliferation, morphogenesis and re-patterning of resident stem cells during caudal fin regeneration in P. latipinna.
在食蚊鱼(Poecilia latipinna)的尾鳍再生过程中,从截肢后立即开始直至新组织获得结构完整性,研究了基质金属蛋白酶(MMP)2和MMP9表达模式的变化。在酶、转录本以及蛋白质水平上研究了这两种MMP的定时表达模式。此外,在再生的三个特定阶段,这两种明胶酶都定位在再生的尾鳍中。结果显示,截肢后1小时(hpa)开始,MMP2的表达逐渐增加,表明其在尾鳍再生早期可能在细胞外基质重塑中发挥作用。然而,在6 hpa和12 hpa阶段,MMP2转录水平的表达降低,这表明可能存在转录调控,以进一步调节其活性。正如在MMP2的情况中所观察到的,MMP9的表达也从1 hpa开始增加,并一直保持升高直至5 dpa。然而,活性MMP9直到12 hpa才出现。此外,这两种明胶酶分别定位在顶端上皮帽以及伤口上皮(1 dpa)和芽基(60 hpa)阶段的进展区。此外,在早期分化阶段(5 dpa),与附近组织相比,MMP2和MMP9在新形成的鳍条中定位的强度较高。基于这些结果,可以推断,从1 hpa直到早期分化阶段,MMP2和MMP9的受控上调确保了细胞外基质的调节性消化,这可能有助于食蚊鱼尾鳍再生过程中驻留干细胞的募集、增殖、形态发生和重新模式化。