RNA-induced inflammation and migration of precursor neurons initiates neuronal circuit regeneration in zebrafish.

Tissue regeneration and functional restoration after injury are considered as stem- and progenitor-cell-driven processes. In the central nervous system, stem cell-driven repair is slow and problematic because function needs to be restored rapidly for vital tasks. In highly regenerative vertebrates, such as zebrafish, functional recovery is rapid, suggesting a capability for fast cell production and functional integration. Surprisingly, we found that migration of dormant "precursor neurons" to the injury site pioneers functional circuit regeneration after spinal cord injury and controls the subsequent stem-cell-driven repair response. Thus, the precursor neurons make do before the stem cells make new. Furthermore, RNA released from the dying or damaged cells at the site of injury acts as a signal to attract precursor neurons for repair. Taken together, our data demonstrate an unanticipated role of neuronal migration and RNA as drivers of neural repair.

Head regeneration and polarity reversal inHydra attenuata can occur in the absence of DNA synthesis.

Regeneration in hydra is considered to be morphallactic because it can occur in the absence of cell division. Whether DNA synthesis is required for regeneration or other repatterning events is not known. The question was investigated by blocking DNA synthesis with hydroxyurea and examining several developmental processes. Head regeneration, reversal of regeneration polarity and battery cell differentiation all took place in the absence of DNA synthesis. Hence, morphallactic regulation in hydra is independent of both DNA synthesis and mitosis.

Assessment of cell proportions during regeneration ofDileptus anser (Ciliata).

Following transection ofDileptus regulation of cell shape and cortical pattern was studied during regeneration in an attempt to understand the interrelations of these two regulation processes. The cell ofDileptus consists of two regions, proboscis and trunk, with the oral structures marking the border between them. The isolated proboscis is able to reorganize into a complete and correctly proportioned organism and the course of this reorganisation has been observed.Correct cell proportions take more than 24h to be established. Three hours after the operation the new border between proboscis and trunk is formed. Initially, the proportions of the cell are far from normal; moreover, they can temporarily change towards a more abnormal state. This indicates that the localisation of the border between the two cell regions and the assessment of final cell proportions are separate phenomena possibly controlled by different mechanisms.