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J Thorac Cardiovasc Surg 2001;121:598-599
© 2001 The American Association for Thoracic Surgery
Letters to the Editor |
Department of Cardiovascular Surgery
Tohoku University Graduate School of Medicine
1-1, Seiryo-machi, Aoba-ku
Sendai 980-8574, Japan
To the Editor:
We read with interest the article by de Haan and associates
1 on heat shock protein 72 (HSP 72). We agree that ischemic pretreatment could not induce tolerance to a severe (26 minutes) spinal cord ischemic insult. However, we have one question. The authors have not demonstrated whether HSP 72 was induced in motor neurons or not. In experimental models of spinal cord ischemia, the main topic has been believed to be the selective vulnerability of motor neurons. Therefore, histologic study is important. Some researchers have counted the number of motor neurons after spinal cord ischemia.
2,3 The authors demonstrated that 15 minutes of spinal cord ischemia was considerably shorter than de Haan's ischemic models (26 minutes). However, our previous report has demonstrated selective motor neuron death after 15 minutes of spinal cord ischemia, and HSP 72 messenger RNA and protein were induced only in motor neurons.
4 Our result revealed that HSP 72 messenger RNA and protein were induced as a set of markers of "neuronal injury" after ischemia. The authors did not say whether HSP 72 was a marker of neuronal injury or a molecular chaperone. Therefore, they should demonstrate temporal profiles of HSP 72 in a histochemical study or an in situ hybridization study.
12/8/113172
doi:10.1067/mtc.2001.113172
References
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