Redman R S, Ball W D, Mezey E, Key S
Oral Pathology Research Laboratory (151-I), Department of Veterans Affairs Medical Center, 50 Irving Street NW, Washington, DC 20422, USA.
Biotech Histochem. 2009 Dec;84(6):253-60. doi: 10.3109/10520290903081377.
The salivary glands often are severely and permanently damaged by therapeutic irradiation for cancer of the head and neck. The markedly reduced quantity and quality of saliva results in greatly increased susceptibility to dental caries and infection of the oral mucosa and alveolar bone. Recently, subcapsular injection of cultured mouse salivary gland cells has achieved a significant degree of regeneration in a previously irradiated mouse salivary gland; however, the recovery was limited to one lobule. We describe here a method for delivering donor rat salivary gland cells via the main duct that distributes several thousand cells throughout the recipient rat's salivary gland. The donated cells exhibited the cytodifferentiation of the structures in which they lodged, i.e., acini, granular convoluted tubules, and the several types of ducts. This method may facilitate the simultaneous functional recovery of almost all of the lobules of irradiated rat salivary glands.
唾液腺常因头颈部癌症的放射治疗而受到严重且永久性的损伤。唾液量和质的显著减少导致患龋齿以及口腔黏膜和牙槽骨感染的易感性大大增加。最近,在先前接受过辐射的小鼠唾液腺中,经包膜下注射培养的小鼠唾液腺细胞已实现了显著程度的再生;然而,恢复仅限于一个小叶。我们在此描述一种通过主导管递送供体大鼠唾液腺细胞的方法,该方法可将数千个细胞分布于受体大鼠的整个唾液腺中。捐赠的细胞在其所在的结构中表现出细胞分化,即腺泡、颗粒曲管以及几种类型的导管。这种方法可能有助于辐照大鼠唾液腺几乎所有小叶同时实现功能恢复。