|ZFIN ID: ZDB-PUB-210225-1|
Injury-induced Cavl-expressing cells at lesion rostral side play major roles in spinal cord regeneration
Zeng, C.W., Kamei, Y., Shigenobu, S., Sheu, J.C., Tsai, H.J.
|Source:||Open Biology 11: 200304 (Journal)|
|Registered Authors:||Tsai, Huai-Jen|
|Keywords:||axon, caveolin-1, motoneuron, neuronal regeneration, spinal cord injury, transgenic zebrafish|
|PubMed:||33622104 Full text @ Open Biol.|
Zeng, C.W., Kamei, Y., Shigenobu, S., Sheu, J.C., Tsai, H.J. (2021) Injury-induced Cavl-expressing cells at lesion rostral side play major roles in spinal cord regeneration. Open Biology. 11:200304.
ABSTRACTThe extent of cellular heterogeneity involved in neuronal regeneration after spinal cord injury (SCI) remains unclear. Therefore, we established stress-responsive transgenic zebrafish embryos with SCI. As a result, we found an SCI-induced cell population, termed SCI stress-responsive regenerating cells (SrRCs), essential for neuronal regeneration post-SCI. SrRCs were mostly composed of subtypes of radial glia (RGs-SrRCs) and neuron stem/progenitor cells (NSPCs-SrRCs) that are able to differentiate into neurons, and they formed a bridge across the lesion and connected with neighbouring undamaged motor neurons post-SCI. Compared to SrRCs at the caudal side of the SCI site (caudal-SrRCs), rostral-SrRCs participated more actively in neuronal regeneration. After RNA-seq analysis, we discovered that caveolin 1 (cav1) was significantly upregulated in rostral-SrRCs and that cav1 was responsible for the axonal regrowth and regenerative capability of rostral-SrRCs. Collectively, we define a specific SCI-induced cell population, SrRCs, involved in neuronal regeneration, demonstrate that rostral-SrRCs exhibit higher neuronal differentiation capability and prove that cav1 is predominantly expressed in rostral-SrRCs, playing a major role in neuronal regeneration after SCI.
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