Chronic-Pain-Associated Astrocytic Reaction in the Spinal Cord Dorsal Horn of Human Immunodeficiency Virus-Infected Patients

被引:145
作者
Shi, Yuqiang [1 ]
Gelman, Benjamin B. [1 ,2 ]
Lisinicchia, Joshua G. [2 ]
Tang, Shao-Jun [1 ]
机构
[1] Univ Texas Med Branch, Dept Neurosci & Cell Biol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
NECROSIS-FACTOR-ALPHA; ATTENUATES MECHANICAL ALLODYNIA; ACTIVATED PROTEIN-KINASE; PRIMARY SENSORY NEURONS; NEUROPATHIC PAIN; NERVE LIGATION; RAT MODELS; CENTRAL SENSITIZATION; MURINE MODELS; CONTRIBUTES;
D O I
10.1523/JNEUROSCI.5628-11.2012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Studies with animal models have suggested that reaction of glia, including microglia and astrocytes, critically contributes to the development and maintenance of chronic pain. However, the involvement of glial reaction in human chronic pain is unclear. We performed analyses to compare the glial reaction profiles in the spinal dorsal horn (SDH) from three cohorts of sex- and age-matched human postmortem tissues: (1) HIV-negative patients, (2) HIV-positive patients without chronic pain, and (3) HIV patients with chronic pain. Our results indicate that the expression levels of CD11b and Iba1, commonly used for labeling microglial cells, did not differ in the three patient groups. However, GFAP and S100 beta, often used for labeling astrocytes, were specifically upregulated in the SDH of the "pain-positive" HIV patients but not in the "pain-negative" HIV patients. In addition, proinflammatory cytokines, TNF alpha and IL-1 beta, were specifically increased in the SDH of pain-positive HIV patients. Furthermore, proteins in the MAPK signaling pathway, including pERK, pCREB and c-Fos, were also upregulated in the SDH of pain-positive HIV patients. Our findings suggest that reaction of astrocytes in the SDH may play a role during the maintenance phase of HIV-associated chronic pain.
引用
收藏
页码:10833 / 10840
页数:8
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