Subcellular Ca2+ signals underlying waves and graded responses in HeLa cells

被引:85
作者
Bootman, MD
Berridge, MJ
机构
[1] Babraham Inst. Lab. of Molec. Sign., Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, Downing Street
关键词
D O I
10.1016/S0960-9822(02)00609-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Many agonist-evoked intracellular Ca2+ signals have a complex spatio-temporal arrangement, and are observed as repetitive Ca2+ spikes and Ca2+ waves. The key to revealing how these complex signals are generated lies in understanding the functional structure of the intracellular Ca2+ pool, Previous imaging studies, using relatively large cells such as oocytes and myocytes, have identified subcellular elementary Ca2+ signals, indicating that the intracellular Ca2+ pool releases Ca2+ from functionally discrete sites. However, it is unclear whether the intracellular Ca2+ pool in smaller cells has a similar architecture, and how such subcellular signals would contribute to global spikes and waves. Results: We detected subcellular Ca2+ signals during the response of single Fura2-loaded HeLa cells to histamine, The spatio-temporal properties of some of these signals were similar to the elementary Ca2+ signals observed in other cells, Subcellular Ca2+ signals were particularly obvious during the 'pacemaker' Ca2+ rise that preceded the regenerative Ca2+ wave. During this pacemaker, the Ca2+ signals were observed initially in the region from which the Ca2+ wave originated, but became more widespread and frequent until a Ca2+ wave was spawned, Similar localized signals were seen during the post-wave Ca2+ increase, and during the low-amplitude Ca2+ responses evoked by threshold histamine concentrations. Conclusions: The intracellular Ca2+ pool in HeLa cells is composed of many functionally discrete units. Upon stimulation, these units produce localized Ca2+ signals. The sequential activation and summation of these units results in Ca2+ wave propagation and, furthermore, the differential recruitment of these units may underlie the graded amplitude of the intracellular Ca2+ signals.
引用
收藏
页码:855 / 865
页数:11
相关论文
共 55 条
[1]   A SINGLE-POOL MODEL FOR INTRACELLULAR CALCIUM OSCILLATIONS AND WAVES IN THE XENOPUS-LAEVIS OOCYTE [J].
ATRI, A ;
AMUNDSON, J ;
CLAPHAM, D ;
SNEYD, J .
BIOPHYSICAL JOURNAL, 1993, 65 (04) :1727-1739
[2]   Expression and function of ryanodine receptors in nonexcitable cells [J].
Bennett, DL ;
Cheek, TR ;
Berridge, MJ ;
DeSmedt, H ;
Parys, JB ;
Missiaen, L ;
Bootman, MD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6356-6362
[3]   INOSITOL TRISPHOSPHATE AND CALCIUM SIGNALING [J].
BERRIDGE, MJ .
NATURE, 1993, 361 (6410) :315-325
[4]   CYTOSOLIC CALCIUM OSCILLATORS [J].
BERRIDGE, MJ ;
GALIONE, A .
FASEB JOURNAL, 1988, 2 (15) :3074-3082
[5]  
BERRIDGE MJ, 1996, RYANODINE RECEPTORS, P119
[6]  
BEZPROZVANNY I, 1995, J MEMBRANE BIOL, V145, P205
[7]   BELL-SHAPED CALCIUM-RESPONSE CURVES OF INS(1,4,5)P3-GATED AND CALCIUM-GATED CHANNELS FROM ENDOPLASMIC-RETICULUM OF CEREBELLUM [J].
BEZPROZVANNY, I ;
WATRAS, J ;
EHRLICH, BE .
NATURE, 1991, 351 (6329) :751-754
[8]   QUESTIONS ABOUT QUANTAL CA(2+) RELEASE [J].
BOOTMAN, M .
CURRENT BIOLOGY, 1994, 4 (02) :169-172
[9]   Extracellular calcium concentration controls the frequency of intracellular calcium spiking independently of inositol 1,4,5-trisphosphate production in HeLa cells [J].
Bootman, MD ;
Young, KW ;
Young, JM ;
Moreton, RB ;
Berridge, MJ .
BIOCHEMICAL JOURNAL, 1996, 314 :347-354
[10]  
BOOTMAN MD, 1994, J BIOL CHEM, V269, P24783