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
相关论文
共 50 条
  • [31] Effects of transmural field stimulation in isolated smooth muscle of human rectum and internal anal sphincter
    Glavind, EB
    Forman, A
    Madsen, G
    Tottrup, A
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1997, 272 (05): : G1075 - G1082
  • [32] Animal model for angiotensin II effects in the internal anal sphincter smooth muscle: mechanism of action
    Fan, YP
    Puri, RN
    Rattan, S
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 282 (03): : G461 - G469
  • [33] Development of a 3-dimensional physiological model of the human internal anal sphincter bioengineered in-vitro from human IAS smooth muscle cells
    Somara, Sita
    Farokhrani, Amin
    Gilmont, Robert R.
    Bitar, Khalil N.
    GASTROENTEROLOGY, 2007, 132 (04) : A588 - A588
  • [34] SMOOTH-MUSCLE RELAXATION AND MEMBRANE HYPERPOLARIZATION IN THE GUINEA-PIG INTERNAL ANAL-SPHINCTER
    MUIR, TC
    STIRRAT, AA
    BRITISH JOURNAL OF PHARMACOLOGY, 1988, 95 : P623 - P623
  • [35] Mechanism of action of angiotensin II (Ang II) in the internal anal sphincter (IAS) smooth muscle.
    Rattan, S
    Puri, R
    Greene, A
    Fan, YP
    GASTROENTEROLOGY, 2001, 120 (05) : A396 - A396
  • [36] CHARACTERIZATION OF MUSCARINIC RECEPTORS IN CULTURED HUMAN IRIS SPHINCTER AND CILIARY SMOOTH-MUSCLE CELLS
    WOLDEMUSSIE, E
    FELDMANN, BJ
    CHEN, JN
    EXPERIMENTAL EYE RESEARCH, 1993, 56 (04) : 385 - 392
  • [37] Isolation of internal and external sphincter progenitor cells from the human anal sphincter with or without radiotherapy
    Son, I. T.
    Lee, H. S.
    Ihn, M. H.
    Lee, K. H.
    Kim, D. -W.
    Lee, K. -W.
    Kim, J. -S.
    Kang, S. -B.
    COLORECTAL DISEASE, 2019, 21 (01) : 38 - 47
  • [38] Translocation of AT1- and AT2-receptors by higher concentrations of angiotensin II in the smooth muscle cells of rat internal anal sphincter
    de Godoy, Marcio A. F.
    Rattan, Satish
    JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 319 (03): : 1088 - 1095
  • [39] Effects of angiotensin II (Ang II)in the internal anal sphincter (IAS) versus the lower esophageal sphincter (LES) smooth muscle.
    Fan, YP
    Puri, P
    Greene, AS
    Rattan, S
    GASTROENTEROLOGY, 2000, 118 (04) : A831 - A831
  • [40] Anatomy of the smooth muscle structure in the female anorectal anterior wall: convergence and anterior extension of the internal anal sphincter and longitudinal muscle
    Muro, S.
    Tsukada, Y.
    Harada, M.
    Ito, M.
    Akita, K.
    COLORECTAL DISEASE, 2019, 21 (04) : 472 - 480