Identification and characterization of neuronal precursors and their progeny from human fetal tissue - PubMed (original) (raw)

Comparative Study

. 2001 Nov 1;66(3):356-68.

doi: 10.1002/jnr.1228.

Affiliations

Comparative Study

Identification and characterization of neuronal precursors and their progeny from human fetal tissue

D R Piper et al. J Neurosci Res. 2001.

Abstract

We have examined primary human neuronal precursors (HNPs) from 18-22-week-old fetuses. We showed that E-NCAM/MAP2/beta-III tubulin-immunoreactive neuronal precursors divide in vitro and could be induced to differentiate into mature neurons in 2 weeks. HNPs did not express nestin and differentiated slowly compared to rodent neuronal restricted precursors (NRPs, 5 days). Immunocytochemical and physiological analyses showed that HNPs could generate a heterogeneous population of neurons that expressed neurofilament-associated protein and various neurotransmitters, neurotransmitter synthesizing enzymes, voltage-gated ion channels, and ligand-gated neurotransmitter receptors and could fire action potentials. Undifferentiated and differentiated HNPs did not coexpress glial markers. Only a subset of cells that expressed GFP under the control of the Talpha1 tubulin promoter was E-NCAM/beta-III tubulin-immunoreactive, indicating nonexclusive overlap between these two HNP cell populations. Overall, HNPs resemble NRPs isolated from rodent tissue and appear to be a neuronal precursor population.

Copyright 2001 Wiley-Liss, Inc.

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Figures

Fig. 1

Fig. 1

Human neuronal precursors were mitotic and E-NCAM+. First-passage cells were acutely dissociated, plated, and processed for immunocytochemistry 48 hr later. A: First-passage HNPs displayed IR for E-NCAM (A, red) and β-III tubulin (A″, green). DAPI staining of nuclei (A′, blue) shows that only a subset of the cells expresses neuronal markers. β-III Tubulin+ and E-NCAM+ cells (B,C, green) incorporated BrdU (B,C, red), indicating that they were mitotic (arrowheads indicate double-labeled cells). β-III Tubulin+ cells (D, red) coexpressed another neuronal-specific protein, MAP2 (D′, green). β-III Tubulin+ cells (F, green, and G, red) did not coexpress the glial markers A2B5 (F, red) or GFAP (G, green). Staining was performed on two or three dishes of cells from four different isolations. E shows human NRP antigenic profiles.

Fig. 2

Fig. 2

HNPs do not coexpress nestin. Acutely dissociated human neural cells were grown for 5 days in culture, pulsed with BrdU for 16 hr (E,F), fixed, and processed for immunocytochemistry to detect the expression of nestin (A,B,D,F, red, and C,E, green) and GFAP (B, green), E-NCAM (C, red), β-III tubulin (D,F green), and BrdU (E, red, and F, blue). DAPI staining (A, blue) was used to identify all cells. Large numbers of nestin+ cells were present in culture and made up about 70% of the total cell population (A). About 15% of the nestin+ cells coexpressed GFAP IR (B, arrowheads), although a few GFAP+ cells did not express nestin (B, arrows). Five percent of the E-NCAM+ cells were nestin+ (C, arrowheads), but none of the β-III tubulin+ cells was nestin+ (D). BrdU labeling identified dividing cells (E,F) and showed that BrdU incorporation was seen in both nestin+ (E,F, arrowhead) and nestin− (E,F, arrow) cells. Triple labeling showed that some of the nestin−, BrdU+ cells (F, arrowheads) were β-III tubulin+ (green). Only 5% of the β-III tubulin+ cells incorporated BrdU, and postmitotic BrdU−, nestin−, β-III tubulin+ cells were also seen (F, arrow, green). Staining was performed on two or three dishes of cells from four different isolations.

Fig. 3

Fig. 3

Differentiating HNPs arrested mitosis and expressed RT-97. First-passage cells (A–E) were compared with cells maintained in cultures for 14 days (A′–E′) under differentiating conditions as described in Materials and Methods. Cells were fixed and processed for immunocytochemistry in parallel. Differentiated cultures contained many mature cells with neuronal morphologies compared with first-passage cells (A,A′). Acutely passaged cultures contained dividing BrdU+ (B, red) β-III tubulin+ (B, green) cells, whereas differentiated cultures contained β-III tubulin+ neurons (B′, green) that had exited the cell cycle (B′ shows one BrdU+ cell, red). β-III Tubulin+ cells (C, green) in acute cultures maintained simple morphologies; those in differentiated cultures extended presumptive neurites (C′, green). D: Acute cells did not contain process-specific RT-97 IR (D, red); nuclear staining is a cross-reactive nuclear epitope. Differentiated neurons expressed RT-97 IR on presumptive neurites (D′, red). Acute cells did not express neurofilament (E, NF-150, red, and DAPI, blue, to illustrate cells in the field), although NF-150-expressing cells were seen after 14 DIC (E′, red). Staining was performed on two or three dishes of cells from two different isolations.

Fig. 4

Fig. 4

Differentiating HNPs expressed synaptophysin and neurotransmitter-synthesizing enzymes. Cells were maintained under differentiating conditions for 14 DIC and processed for immunocyto-chemistry for E-NCAM (A), synaptophysin (A′), glutamate (B), glycine (C), TH (D), and ChAT (E). A single cell exhibiting synaptophysin IR is shown (A′), and expression colocalizes with that of E-NCAM (A). Subsets of cells express IR for glutamate (B, arrowhead), glycine (C, arrowhead), TH (D, arrowhead), and ChAT (E, arrowhead), whereas other cells are negative (B–E, arrows). Staining was performed on two or three dishes of cells from two different isolations.

Fig. 5

Fig. 5

E-NCAM+ HNPs immunoidentified for patch-clamp and fura-2 recordings. Shown are mixed human cell cultures from undifferentiated conditions (A) or following 14 days under differentiating conditions (B), visualized using Hoffman optics. The cells were live stained for E-NCAM (red in A′**, B′). A composite Hoffman-fluorescence image (A″, B**″) shows the red E-NCAM+ HNPs from which whole-cell currents were recorded (arrows). Identical methods were used to identify E-NCAM+ cells used for Ca2+ imaging experiments.

Fig. 6

Fig. 6

Differentiating HNPs expressed voltage-gated Na+ and K+ channels and fired action potentials. A: Whole-cell voltage-clamp recordings were made from E-NCAM+ HNPs in acutely passaged conditions (A1,A2) or following differentiation (A3). Cells were held at −100 mV and stepped to test voltages between −80 and 80 mV in 10 mV increments. Both of the acute HNPs expressed outward K+ currents (A1,A2), but only one exhibited a small inward Na+ current (A2). A differentiated HNP expressed both outward K+ and inward Na+ currents (A3). B1–3: Peak outward K+ currents (triangles) and peak inward Na+ currents (circles) were plotted against the command voltage for the cells represented in A. C: HNPs under acutely passaged conditions failed to fire action potentials (C1,C2); in contrast, a differentiated HNP fired an action potential when stimulated with depolarizing current injections (C3). Inset in C3 shows the action potential overshoot on a longer time scale.

Fig. 7

Fig. 7

Differentiating HNPs expressed functional neurotransmitter receptors. A,B: Ratiometric imaging of acute and differentiating E-NCAM+ HNP cells. Ratio of fura-2 emission (I340/I380, left y axis) with approximate Ca2+ concentrations ([Ca2+]i, right y axis). Arrow-heads and labels show application of neurotransmitters. All substances were applied at 500 μM, except for K50, which was 50 mM K+ HR. A: An acutely passaged HNP responded only to acetylcholine (ACh), with small magnitude. B: A differentiated neuron responded to GABA, glutamate (E), glycine (G), elevated K+ (K50), and ACh. C: Fraction of cells responding to neurotransmitters is shown for acutely passaged cells (open bars, n = 17) and differentiated cells [shaded bars, n = 70, except for norepinephrine (NE), for which n = 43]. Acute HNPs did not respond to GABA, glycine, dopamine (DA), NE, or ascorbic acid (AA) control. Differentiated neurons responded to all substances with higher frequencies, but only ACh and NE were significant (asterisks). D: The distribution of response amplitudes is shown by the box plot of acute (left box, open circles) and differentiating cells (Diff; right box, gray circles). Squares represent distribution mean, box represents the 75th percentiles, error bars represent the 95th percentiles, and circles plot the individual response amplitudes. Experiments were performed on a total of six dishes of cells from three different isolations.

Fig. 8

Fig. 8

Subset of E-NCAM- and β-III tubulin-immunoreactive HNPs coexpresses α-tubulin promoter-driven GFP. Tα1:GFP constructs were transfected into day 2 cultures of fetal neural cells. GFP expression (A,A′**, A″, B,C,D**, green) was seen in cells with neuronal morphology as early as 24 hr after transfection. Plates were fixed and processed for E-NCAM IR (B, inset, B′, red), β-III tubulin (C, red), and GFAP (D, red). The inset shows lack of colocalization for Tα1:GFP (green) and E-NCAM (red). We show one Tα1:GFP+ cell that was E-NCAM+ (B,B′, arrowhead) and one that was β;-III tubulin+ (C, arrowhead). None of the Tα1:GFP-expressing cells was GFAP+ (arrows in C and D show lack of colocalization). These experiments were performed on two or three dishes of cells from three different isolations.

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