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使用TED3和ZeHB3作为分子标记分析伤口诱导的血管再生早期过程。

Analysis of early processes in wound-induced vascular regeneration using TED3 and ZeHB3 as molecular markers.

作者信息

Nishitani Chikako, Demura Taku, Fukuda Hiroo

机构信息

Department of Biological Sciences, Graduate School of Science, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan.

出版信息

Plant Cell Physiol. 2002 Jan;43(1):79-90. doi: 10.1093/pcp/pcf008.

Abstract

Interruption of the vascular bundles of Zinnia internodes induced transdifferentiation of cells into tracheary elements (TEs) or sieve elements (SEs) within 4 d of wounding. The early stage of the regeneration processes was analyzed using two molecular marker genes, TED3 and ZeHB3, which are expressed specifically in TE precursor cells and immature phloem cells, respectively. An increase in the numbers of TED3 and ZeHB3 mRNA-expressing cells always preceded an increase in the numbers of TEs and SEs formed. The earliest sign of vascular differentiation was the appearance 24 h after wounding of a layer(s) of TED3 mRNA-expressing cells in the inter- and intrafascicular cambial-like regions along the severed vascular bundles. In contrast, the number of ZeHB3 mRNA-expressing cells decreased dramatically along the severed bundles 24 h after wounding, and increased again 36 h after wounding. These results clearly indicate that xylem and phloem differentiation are not synchronized during vascular regeneration. Treatment with 10(-3) M colchicine abolished the expression of ZeHB3 mRNA in pith parenchyma, but not TED3 mRNA; this suggests that cell division is a prerequisite for the transdifferentiation of pith parenchymal cells into immature phloem cells expressing ZeHB3. In contrast, transdifferentiation of pith parenchymal cells to TE precursor cells does not require preceding cell division. However, the inhibition of cell division prevented the formation of both radial files of TEs and the cambial-like layer(s) of TED3 mRNA-expressing cells, and, ultimately, vascular regeneration altogether. These results imply that wound-induced cambial-like activity in and between severed vascular bundles is essential for vascular regeneration.

摘要

百日菊节间维管束的中断会导致细胞在受伤后4天内转分化为管状分子(TEs)或筛管分子(SEs)。利用两个分子标记基因TED3和ZeHB3分析了再生过程的早期阶段,这两个基因分别在TE前体细胞和未成熟韧皮部细胞中特异性表达。TED3和ZeHB3 mRNA表达细胞数量的增加总是先于所形成的TEs和SEs数量的增加。血管分化的最早迹象是在受伤后24小时,沿着切断的维管束,束间和束内形成层样区域出现一层表达TED3 mRNA的细胞。相反,受伤后24小时,沿着切断的维管束,表达ZeHB3 mRNA的细胞数量急剧减少,受伤后36小时再次增加。这些结果清楚地表明,在血管再生过程中木质部和韧皮部的分化并不同步。用10^(-3) M秋水仙碱处理可消除髓薄壁组织中ZeHB3 mRNA的表达,但不影响TED3 mRNA的表达;这表明细胞分裂是髓薄壁组织细胞转分化为表达ZeHB3的未成熟韧皮部细胞的先决条件。相反,髓薄壁组织细胞向TE前体细胞的转分化不需要先进行细胞分裂。然而,细胞分裂的抑制阻止了TEs的径向排列和表达TED3 mRNA的形成层样层的形成,最终完全阻止了血管再生。这些结果表明,伤口诱导的切断维管束内和之间的形成层样活性对于血管再生至关重要。

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