Chang L Y, Wu R, Nettesheim P
J Cell Sci. 1985 Mar;74:283-301. doi: 10.1242/jcs.74.1.283.
The purpose of our studies was to determine the fate of different cell types present in early primary cultures of tracheal epithelial cells and, if possible, to elucidate the role they play in the establishment of the cultures. Epithelial cells were isolated from rat tracheas with 0.5% Pronase and were cultured on collagen-coated dishes as described previously. Light and transmission electron microscopic studies showed that the cell population harvested from rat trachea was composed of approximately 30% ciliated cells, 50% granule-containing cells and 20% undifferentiated cells (presumably basal cells). Upon seeding the tracheal cell suspensions into culture, approximately 40% of the cells attached. Cell attachment was virtually complete after 16 h. Roughly 60% of the cells attaching during the first 12 h were neither ciliated nor granulated, suggesting that undifferentiated cells played a major role in establishment of the early cultures. Between 20 and 35% of the cells attaching during this time were identified as granulated cells (mucous cells). Ciliated cells did not start to attach in significant numbers until 8 h after seeding. They never amounted to more than 8-12% of the attached cell population. After 12 h of culture, the cell population underwent a progressive loss of differentiation. The number of poorly differentiated cells (i.e. those showing neither cilia nor mucous granules) increased correspondingly. This loss of differentiation preceded the onset of DNA synthesis and cell growth which began at about 24 and 40 h, respectively. Continuous [3H]thymidine-labelling studies showed that at 48 h after the start of culture about 90% of all attached cells had entered DNA synthesis at least once. This finding is consistent with the interpretation that the ciliated cells are terminally differentiated cells and are probably the only part of the tracheal cell inoculum not participating in the growth of the cultures. At 72 h, the cultures (now in mid-log growth phase) were composed of uniformly undifferentiated cells lacking cilia and mucous granules. The cells nevertheless showed unequivocal epithelial characteristics such as tight junctions and desmosomes. The studies suggest that both basal and mucous cells are responsible for the establishment and growth of the rat tracheal epithelial cell cultures.
我们研究的目的是确定气管上皮细胞早期原代培养物中不同细胞类型的命运,并在可能的情况下阐明它们在培养物建立过程中所起的作用。用0.5%的链霉蛋白酶从大鼠气管中分离上皮细胞,并如前所述在胶原包被的培养皿上进行培养。光镜和透射电镜研究表明,从大鼠气管收获的细胞群体约由30%的纤毛细胞、50%的含颗粒细胞和20%的未分化细胞(可能是基底细胞)组成。将气管细胞悬液接种到培养物中后,约40%的细胞附着。16小时后细胞附着基本完成。在前12小时内附着的细胞中,约60%既无纤毛也无颗粒,这表明未分化细胞在早期培养物的建立中起主要作用。在此期间附着的细胞中,20%至35%被鉴定为含颗粒细胞(黏液细胞)。纤毛细胞直到接种后8小时才开始大量附着。它们在附着细胞群体中所占比例从未超过8%至12%。培养12小时后,细胞群体的分化逐渐丧失。分化不良的细胞(即既无纤毛也无黏液颗粒的细胞)数量相应增加。这种分化丧失先于分别在约24小时和40小时开始的DNA合成和细胞生长。连续的[3H]胸腺嘧啶核苷标记研究表明,培养开始后48小时,所有附着细胞中约90%至少进入过一次DNA合成。这一发现与以下解释一致,即纤毛细胞是终末分化细胞,可能是气管细胞接种物中唯一不参与培养物生长的部分。72小时时,培养物(此时处于对数生长中期)由缺乏纤毛和黏液颗粒的均匀未分化细胞组成。然而,这些细胞显示出明确的上皮特征,如紧密连接和桥粒。这些研究表明,基底细胞和黏液细胞都对大鼠气管上皮细胞培养物的建立和生长负责。