Yan L, Leontovich A, Fei K, Sarras M P
Department of Anatomy, University of Kansas Medical Center, Kansas City, Kansas, 66160-7400, USA.
Dev Biol. 2000 Mar 1;219(1):115-28. doi: 10.1006/dbio.1999.9568.
The newly emerging astacin metalloproteinase family comprises multiple members with diverse functions. Most recently, the development-related functions have been attributed to both (1) proteolytic cleavage and subsequent release of active TGF-beta-like growth factors from latent inhibitory complexes and (2) modification of extracellular matrix (ECM) assembly and composition. We previously identified and purified hydra metalloproteinase 1 (HMP-1), a developmentally important astacin proteinase that functions in head regeneration and transdifferentiation of tentacle battery cells (L. Yan et al., 1995, Development 121, 1591-1602). In the present study, further cloning revealed that HMP-1 is produced as a secreted zymogen with a conserved hydrophobic signal sequence and a putative propeptide. The processed HMP-1 is composed of a characteristic astacin proteinase domain and a unique Cys-rich C-terminus. With this simple domain structure, HMP-1 represents an ancestral astacin proteinase. Consistent with its role in head regeneration, HMP-1 mRNA is expressed at highest levels by endodermal cells at the apical pole of the body column just inferior to the base of tentacles, the region of active cell differentiation or transdifferentiation. A modified immunocytochemical procedure demonstrated that HMP-1 protein can be localized not only to ECM of tentacles as we previously reported, but also to endodermal cells of the body column in a pattern similar to its mRNA distribution. The localization of HMP-1 protein in tentacles was confirmed using an enzymatic approach. A translocation of HMP-1 protein from cells in the body column to the extracellular milieu in tentacles further suggests that HMP-1 is a secreted protein. HMP-1 expression undergoes extensive regulation at the transcriptional level both temporally and spatially during head regeneration. The involvement of HMP-1 in this morphogenetic process is further supported by the blockage of head regeneration with localized antisense treatment. Taken together, these results suggest that HMP-1 is a secreted astacin metalloproteinase that has an important role in regulating hydra head morphogenesis potentially through its differential expression along the body axis.
新出现的虾红素金属蛋白酶家族包含多个具有不同功能的成员。最近,与发育相关的功能被归因于两个方面:(1)蛋白水解切割以及随后从潜在抑制复合物中释放出活性转化生长因子-β样生长因子;(2)对细胞外基质(ECM)组装和组成的修饰。我们之前鉴定并纯化了水螅金属蛋白酶1(HMP-1),这是一种在发育中具有重要作用的虾红素蛋白酶,其在头部再生和触手电池细胞的转分化过程中发挥作用(L. Yan等人,1995年,《发育》121卷,1591 - 1602页)。在本研究中,进一步克隆显示HMP-1作为一种分泌型酶原产生,具有保守的疏水信号序列和一个假定的前肽。加工后的HMP-1由一个特征性的虾红素蛋白酶结构域和一个独特的富含半胱氨酸的C末端组成。凭借这种简单的结构域结构,HMP-1代表了一种原始的虾红素蛋白酶。与其在头部再生中的作用一致,HMP-1 mRNA在体柱顶端极靠近触手基部的内胚层细胞中表达水平最高,该区域是活跃的细胞分化或转分化区域。一种改良的免疫细胞化学方法表明HMP-1蛋白不仅如我们之前报道的那样定位于触手的细胞外基质,还以与其mRNA分布相似的模式定位于体柱的内胚层细胞。使用酶学方法证实了HMP-1蛋白在触手的定位。HMP-1蛋白从体柱细胞向触手细胞外环境的转运进一步表明HMP-1是一种分泌蛋白。在头部再生过程中,HMP-1的表达在转录水平上经历了广泛的时空调节。局部反义处理阻断头部再生进一步支持了HMP-1参与这一形态发生过程。综上所述,这些结果表明HMP-1是一种分泌型虾红素金属蛋白酶,可能通过其沿身体轴的差异表达在调节水螅头部形态发生中发挥重要作用。