Kannan Y, Stead R H, Goldsmith C H, Bienenstock J
Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
J Neurosci Res. 1994 Feb 15;37(3):374-83. doi: 10.1002/jnr.490370309.
Induction of neurite outgrowth from superior cervical ganglia (SCG) by rat lymphoid tissues was studied using a tissue culture model. Neonatal rat SCG were cultured with 6-12-week-old rat thymus, spleen, or mesenteric lymph node (MLN) explants in a Matrigel layer, in defined culture medium without exogenous nerve growth factor (NGF). SCG were also co-cultured with neonatal rat heart (as positive control) or spinal cord (SC; as negative control). To determine whether inflammation affects the ability of lymphoid tissues to induce neurite outgrowth, we also examined MLN at various times after infecting rats with Nip-postrongylus brasiliensis (Nb-MLN). In one series of experiments, a single lymphoid tissue explant was surrounded by four SCG at a distance of 1 mm. The extent of neurite outgrowth was determined by counting the number of neurites 0.5 mm away from each ganglion at several time points. Adult thymus and, to a lesser extent, spleen had strong stimulatory effects on neurite outgrowth from SCG after 12 hr or more in culture. For thymus tissue, this was similar to the positive control heart explants. MLN from normal rats had minimal effect on neurite outgrowth; however, Nb-MLN showed a time-dependent enhancement of the neurite outgrowth, maximal at 3 weeks after infection. The relative efficacy of neurite outgrowth induction (heart > or = thymus > or = Nb-MLN > or spleen > or = MLN > or = SC) was confirmed in a second series of experiments where one SCG was surrounded by three different tissue explants. We then examined the role of 2.5S NGF, a well-known trophic factor for sympathetic nerves, in the lymphoid tissue-induced neurite outgrowth. Anti-NGF treatment of co-cultures of SCG and heart almost completely blocked the neurite outgrowth. Anti-NGF also significantly inhibited thymus- and spleen-induced neurite outgrowth, but not as effectively as heart-induced neuritogenesis (93, 80, and 77% inhibition at 24 hr; 86, 70, and 68% inhibition at 48 hr for heart, thymus, and spleen, respectively). On the other hand, anti-NGF inhibited only 8% of neurite outgrowth induced by 3-week post-infection Nb-MLN at 24 hr, and 41% at 48 hr. These data show that several adult rat lymphoid tissues exert neurotrophic/tropic effects. The predominant growth factor in thymus and spleen is NGF, while Nb-MLN produces factor(s) which is (are) immunologically distinguishable from NGF.(ABSTRACT TRUNCATED AT 400 WORDS)
利用组织培养模型研究了大鼠淋巴组织对颈上神经节(SCG)神经突生长的诱导作用。将新生大鼠的SCG与6 - 12周龄大鼠的胸腺、脾脏或肠系膜淋巴结(MLN)外植体在基质胶层中培养,置于不含外源性神经生长因子(NGF)的限定培养基中。SCG还与新生大鼠心脏(作为阳性对照)或脊髓(SC;作为阴性对照)共同培养。为了确定炎症是否影响淋巴组织诱导神经突生长的能力,我们还在大鼠感染巴西日圆线虫(Nb - MLN)后的不同时间点检查了MLN。在一系列实验中,单个淋巴组织外植体被四个距离为1毫米的SCG包围。通过在几个时间点计数距每个神经节0.5毫米处的神经突数量来确定神经突生长的程度。培养12小时或更长时间后,成年胸腺以及程度稍轻的脾脏对SCG的神经突生长有强烈的刺激作用。对于胸腺组织,这与阳性对照心脏外植体相似。正常大鼠的MLN对神经突生长影响极小;然而,Nb - MLN显示出神经突生长的时间依赖性增强,在感染后3周达到最大值。在另一系列实验中,一个SCG被三种不同的组织外植体包围,证实了神经突生长诱导的相对效力(心脏≥胸腺≥Nb - MLN≥脾脏≥MLN≥SC)。然后我们研究了2.5S NGF(一种众所周知的交感神经营养因子)在淋巴组织诱导的神经突生长中的作用。对SCG和心脏共同培养物进行抗NGF处理几乎完全阻断了神经突生长。抗NGF也显著抑制了胸腺和脾脏诱导的神经突生长,但不如心脏诱导的神经突形成有效(24小时时抑制率分别为93%、80%和77%;48小时时心脏、胸腺和脾脏的抑制率分别为86%、70%和68%)。另一方面,抗NGF在24小时时仅抑制感染后3周的Nb - MLN诱导的神经突生长的8%,48小时时抑制41%。这些数据表明,几种成年大鼠淋巴组织发挥神经营养/向性作用。胸腺和脾脏中的主要生长因子是NGF,而Nb - MLN产生的因子在免疫学上与NGF不同。(摘要截断于400字)