Immunoglobulins from scleroderma patients inhibit the muscarinic receptor activation in internal anal sphincter smooth muscle cells

被引:52
|
作者
Singh, Jagmohan
Mehendiratta, Vaibhav
Del Galdo, Francesco [2 ,3 ]
Jimenez, Sergio A. [2 ,3 ]
Cohen, Sidney
DiMarino, Anthony J.
Rattan, Satish [1 ]
机构
[1] Thomas Jefferson Univ, Jefferson Med Coll, Dept Med, Div Gastroenterol & Hepatol, Philadelphia, PA 19107 USA
[2] Thomas Jefferson Univ, Scleroderma Ctr, Philadelphia, PA 19107 USA
[3] Thomas Jefferson Univ, Jefferson Inst Mol Med, Philadelphia, PA 19107 USA
关键词
systemic sclerosis; rectoanal function; muscarinic receptor; autoantibodies; SYSTEMIC-SCLEROSIS; SJOGRENS-SYNDROME; GASTROINTESTINAL MANIFESTATIONS; ESOPHAGEAL DYSFUNCTION; MYOELECTRIC ACTIVITY; NEURONAL ANTIBODIES; KNOCKOUT MICE; AUTOANTIBODIES; RELAXATION; KINASE;
D O I
10.1152/ajpgi.00286.2009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Singh J, Mehendiratta V, Del Galdo F, Jimenez SA, Cohen S, DiMarino AJ, Rattan S. Immunoglobulins from scleroderma patients inhibit the muscarinic receptor activation in internal anal sphincter smooth muscle cells. Am J Physiol Gastrointest Liver Physiol 297: G1206-G1213, 2009. First published September 24, 2009; doi: 10.1152/ajpgi.00286.2009.-Systemic sclerosis (SSc) IgGs affecting the M-3-muscarinic receptor (M-3-R) have been proposed to be responsible for the gastrointestinal (GI) dysmotility in this disease. However, the effect of SSc IgGs on smooth muscle cell (SMC) function has not been studied. We determined the effect of SSc IgGs on the muscarinic receptor activation by bethanechol (BeCh; methyl derivate of carbachol) in SMC and smooth muscle strips from rat internal anal sphincter. IgGs were purified from GI-symptomatic SSc patients and normal volunteers, with protein G-Sepharose columns. SMC lengths were determined via computerized digital micrometry. The presence of M-3-R and IgG-M-3-R complex was determined by Western blot. IgGs from SSc patients but not from normal volunteers caused significant and concentration-dependent inhibition of BeCh response (P < 0.05). The maximal shortening of 22.2 +/- 1.2% caused by 10(-4) M BeCh was significantly attenuated to 8.3 +/- 1.2% by 1 mg/ml of SSc IgGs (P < 0.05). Experiments performed in smooth muscle strips revealed a similar effect of SSc IgG that was fully reversible. In contrast to the effect on BeCh, the SSc IgGs caused no significant effect (P > 0.05) on K+ depolarization and alpha(1)-adrenoceptor activation by phenylephrine. Western blot studies revealed the specific presence of SSc IgG-M-3-R complex. SSc IgGs attenuated M-3-R activation, which was reversible with antibody removal. These data suggest that SSc GI dysmotility may be caused by autoantibodies that inhibit the muscarinic neurotransmission. Future treatment of SSc patients may be directed at the removal or neutralization of these antibodies.
引用
收藏
页码:G1206 / G1213
页数:8
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