Zhang M, Zola H, Read L, Penttila I
Cooperative Research Centre for Tissue Growth and Repair, Child Health Research Institute, North Adelaide, South Australia, Australia.
Immunol Cell Biol. 2001 Jun;79(3):291-7. doi: 10.1046/j.1440-1711.2001.01013.x.
Transforming growth factor-beta (TGF-beta) is present at high concentrations in maternal milk. In milk TGF-beta2 is the predominant isoform. For function TGF-beta2 requires TbetaRIII to facilitate efficient binding to the TGF-beta receptor types I and II signalling complex. We have shown that TGF-beta receptor types I (TbetaRI), II (TbetaRII) and III (TbetaRIII) are coexpressed in the suckling rat intestine. Immunostaining for TbetaRIII was also observed in the intestinal lumen prior to weaning. TbetaRIII (or betaglycan) has been reported in serum, cell culture medium and extracellular matrix. To determine whether a soluble form of TbetaRIII is present in milk, the rat milk aqueous phase was analysed by slot-blot and Western blot. Soluble TbetaRIII was detected in milk throughout lactation. Western blot analysis of rat milk revealed a high molecular weight band of glycosylated protein of >200 kDa, with a core protein of approximately 110-120 kDa that comigrated with recombinant TbetaRIII. Immunoabsorption of soluble TbetaRIII (sTbetaRIII) from milk resulted in partial depletion of active TGF-beta from milk, suggesting that the receptor may interact with ligand in milk. In addition rat pups suckled on mother's milk demonstrated an enhanced labelling of TbetaRIII in the gut, as compared with pups fed on a rat milk substitute (RMS). These findings suggest that milk sTbetaRIII is functional, and may modulate milk-derived TGF-beta function in the developing intestine.
转化生长因子-β(TGF-β)在母乳中浓度很高。在母乳中,TGF-β2是主要的异构体。就功能而言,TGF-β2需要TβRIII来促进其与I型和II型TGF-β受体信号复合物的有效结合。我们已经证明,I型(TβRI)、II型(TβRII)和III型(TβRIII)TGF-β受体在哺乳大鼠肠道中共同表达。在断奶前的肠腔中也观察到了TβRIII的免疫染色。血清、细胞培养基和细胞外基质中均有TβRIII(或β聚糖)的报道。为了确定母乳中是否存在可溶性TβRIII,通过狭缝印迹和蛋白质印迹分析了大鼠母乳水相。在整个哺乳期的母乳中都检测到了可溶性TβRIII。对大鼠母乳的蛋白质印迹分析显示,有一条大于200 kDa的糖基化蛋白高分子量条带,其核心蛋白约为110 - 120 kDa,与重组TβRIII迁移位置相同。从母乳中免疫吸收可溶性TβRIII(sTβRIII)导致母乳中活性TGF-β部分减少,这表明该受体可能与母乳中的配体相互作用。此外,与喂食大鼠乳替代品(RMS)的幼崽相比,吸食母乳的大鼠幼崽肠道中TβRIII的标记增强。这些发现表明,母乳中的sTβRIII具有功能,并且可能在发育中的肠道中调节源自母乳的TGF-β功能。