Tsonis P A, Trombley M T, Rowland T, Chandraratna R A, del Rio-Tsonis K
Laboratory of Molecular Biology, Department of Biology, University of Dayton, Dayton, Ohio 45469-2320, USA.
Dev Dyn. 2000 Dec;219(4):588-93. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1082>3.0.CO;2-H.
Prompted by the actions of retinoids and their receptors in gene regulation, in the developing eye and especially in the lens, we have undertaken a detailed study to examine the effects of retinoids on urodele lens regeneration. First, we examined the effects of exogenous retinoids. It was found that exogenous retinoids had no significant effect on lens regeneration. However, when synthesis of retinoic acid was inhibited by disulfiram, or when the function of the retinoid receptors was impaired by using a RAR antagonist, the process of lens regeneration was dramatically affected. In the majority of the cases, lens regeneration was inhibited and lens morphogenesis was disrupted. In a few cases, we were also able to observe ectopic lens regeneration from places other than the normal site, which is from the dorsal iris. The most spectacular case was the regeneration of a lens from the cornea, an event possible only in premetamorphic frogs. These data show that inhibition of retinoid receptors is paramount for the normal course and distribution of lens regeneration. We have also examined expression of RAR-delta during lens regeneration. This receptor was expressed highly in the regenerating lens only. Therefore, it seems that this receptor is specific for the regeneration process and consequently such expression correlates well with the effects of RAR inhibition observed in our studies.
受维甲酸及其受体在基因调控、发育中的眼睛尤其是晶状体中的作用所启发,我们开展了一项详细研究,以考察维甲酸对有尾目动物晶状体再生的影响。首先,我们研究了外源性维甲酸的作用。结果发现,外源性维甲酸对晶状体再生没有显著影响。然而,当用双硫仑抑制视黄酸的合成,或者使用视黄酸受体拮抗剂损害视黄酸受体的功能时,晶状体再生过程受到显著影响。在大多数情况下,晶状体再生受到抑制,晶状体形态发生受到破坏。在少数情况下,我们还能够观察到从正常部位(即背侧虹膜)以外的地方异位再生晶状体。最引人注目的例子是从角膜再生出晶状体,这种情况仅在变态前的青蛙中才可能发生。这些数据表明,抑制视黄酸受体对于晶状体再生的正常进程和分布至关重要。我们还研究了视黄酸受体δ(RAR-δ)在晶状体再生过程中的表达。该受体仅在再生的晶状体中高表达。因此,看来这种受体对再生过程具有特异性,其表达与我们研究中观察到的视黄酸受体抑制的效果密切相关。