Weiler E, Farbman A I
Department of Neurobiology and Physiology, Northwestern University, Evanston, Illinois 60208-3520, USA.
Glia. 1998 Apr;22(4):315-28. doi: 10.1002/(sici)1098-1136(199804)22:4<315::aid-glia1>3.0.co;2-2.
It is well known that progenitor cells in the basal layer of olfactory epithelium proliferate continuously throughout life; the offspring of these dividing cells produce replacements for receptor neurons. In the rat the number of proliferating basal cells/mm length of epithelium (proliferation density) decreases with postnatal age while the area of the olfactory sheet increases. The supporting cells, which act as the glia of the olfactory epithelium, also divide. We examined in detail some aspects of the dynamics of olfactory supporting cell proliferation to determine whether their rate of proliferation changes with age, and how it compares with the rate in basal progenitor cells. Using BrdU to label dividing cells, we determined the proliferation density of supporting cells and basal cells in 10 microm coronal sections from six different anterior-posterior regions in rats ranging in age from birth (P1) until P333. We observed a dramatic decrease in supporting cell proliferation density from P1 (80 cells/mm) to P11 (32 cells/mm) to P21 (12 cells/mm); the density decreases continuously to P333 (0.4 cells/mm). This reduction was even more dramatic than that in the basal cell population (Weiler and Farbman, 1997). Analysis of the data for correlation between basal and supporting cell proliferation revealed a weak correlation in neonates but no correlation in older animals. This suggests that the mechanisms that regulate proliferation of the two cell types are different. Our data also indicate that the proliferation of supporting cells is related only to growth in surface area of the epithelium. No turnover seems to occur in the supporting cells as it does in the olfactory neurons, where proliferation of basal cells is necessary for both growth and replacement.
众所周知,嗅觉上皮基底层中的祖细胞在整个生命过程中持续增殖;这些分裂细胞的后代会产生受体神经元的替代细胞。在大鼠中,每毫米上皮长度的增殖基细胞数量(增殖密度)会随着出生后的年龄增长而减少,而嗅板的面积会增加。作为嗅觉上皮神经胶质细胞的支持细胞也会分裂。我们详细研究了嗅觉支持细胞增殖动力学的一些方面,以确定其增殖速率是否随年龄变化,以及与基底祖细胞的增殖速率相比如何。我们使用溴脱氧尿苷(BrdU)标记分裂细胞,测定了从出生(P1)到P333不同年龄大鼠六个不同前后区域的10微米冠状切片中支持细胞和基底细胞的增殖密度。我们观察到支持细胞增殖密度从P1(80个细胞/毫米)急剧下降到P11(32个细胞/毫米)再到P21(12个细胞/毫米);密度持续下降至P333(0.4个细胞/毫米)。这种下降甚至比基底细胞群体的下降更为显著(韦勒和法布曼,1997年)。对基底细胞和支持细胞增殖之间相关性的数据分析显示,新生大鼠中存在微弱相关性,但在成年动物中无相关性。这表明调节这两种细胞类型增殖的机制不同。我们的数据还表明,支持细胞的增殖仅与上皮表面积的增长有关。支持细胞似乎不像嗅觉神经元那样发生更新,在嗅觉神经元中,基底细胞的增殖对于生长和替换都是必要的。