The molecular mechanism of NELL2 movement and secretion in hippocampal progenitor HiB5 cells

被引:3
|
作者
Ha, Chang Man [1 ,2 ,3 ]
Hwang, Eun Mi [1 ,2 ,4 ]
Kim, Eunju [1 ,2 ,4 ]
Lee, Da Yong [4 ]
Chang, Sunghoe [5 ]
Lee, Byung Ju [6 ]
Hong, Seong-Geun [1 ,2 ]
Park, Jae-Yong [1 ,2 ,4 ]
机构
[1] Gyeongsang Natl Univ, Sch Med, Inst Hlth Sci, Dept Physiol, Jinju 660290, South Korea
[2] Gyeongsang Natl Univ, Sch Med, Med Res Ctr Neural Dysfunct, Jinju 660290, South Korea
[3] Korea Brain Res Inst, Convergence Brain Res Dept, Taegu 700010, South Korea
[4] Korea Inst Sci & Technol, Ctr Funct Connect, Seoul 136791, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Biomed Sci, Neurosci Res Inst,Biomembrane Plast Res Ctr, Seoul 110799, South Korea
[6] Univ Ulsan, Dept Biol Sci, Ulsan 680749, South Korea
基金
新加坡国家研究基金会;
关键词
glycoprotein; intracellular movement; NELL2; secretion; EGF-LIKE REPEATS; FAMILY PROTEIN; RAT-BRAIN; IN-VIVO; MOTOR; NEURONS; TRANSPORT; DIFFERENTIATION; KIF3A/B; DOMAIN;
D O I
10.1007/s10059-013-0216-5
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
Neural epidermal growth factor-like protein-like 2 (NELL2) is a secreted glycoprotein that is predominantly expressed in the nervous system, but little is known about the intracellular movement and secretion mechanism of this protein. By monitoring the localization and movements of enhanced green fluorescent protein (EGFP)-labeled NELL2 in living cultured hippocampal neuroprogenitor HiB5 cells, we determined the subcellular localization of NELL2 and its intracellular movement and secretion mechanism. Cterminal EGFP-fused NELL2 showed a typical expression pattern of secreted proteins, especially with respect to its localization in the endoplasmic reticulum, Golgi apparatus, and punctate structures. Vesicles containing NELL2 exhibited bidirectional movement in HiB5 cells. The majority of the vesicles (70.1%) moved in an anterograde direction with an average velocity of 0.454 mu m/s, whereas some vesicles (28.7%) showed retrograde movement with an average velocity of 0.302 mu m/s. The movement patterns of NELL2 vesicles were dependent upon the presence of microtubules in HiB5 cells. Anterograde movement of NELL2 did not lead to a detectable accumulation of NELL2 in the peripheral region of the cell, indicating that it was secreted into the culture medium. We also showed that the N-terminal 29 amino acids of NELL2 were important for secretion of this protein. Taken together, these results strongly suggest that the N-terminal region of NELL2 determines both the pattern of its intracellular expression and transport of NELL2 vesicles by high-velocity movement. Therefore, NELL2 may affect the cellular activity of cells in a paracrine or autocrine manner.
引用
收藏
页码:527 / 533
页数:7
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