One-step immortalization of primary human airway epithelial cells capable of oncogenic transformation
- Jordan L. Smith†1, 2,
- Liam C. Lee†1, 3,
- Abigail Read1,
- Qiuning Li1, 4,
- Bing Yu1, 5,
- Chih-Shia Lee1 and
- Ji Luo1Email authorView ORCID ID profile
© The Author(s) 2016
Received: 15 September 2016
Accepted: 3 November 2016
Published: 11 November 2016
The ability to transform normal human cells into cancer cells with the introduction of defined genetic alterations is a valuable method for understanding the mechanisms of oncogenesis. Easy establishment of immortalized but non-transformed human cells from various tissues would facilitate these genetic analyses.
We report here a simple, one-step immortalization method that involves retroviral vector mediated co-expression of the human telomerase protein and a shRNA targeting the CDKN2A gene locus. We demonstrate that this method could successfully immortalize human small airway epithelial cells while maintaining their chromosomal stability. We further showed that these cells retain p53 activity and can be transformed by the KRAS oncogene.
Our method simplifies the immortalization process and is broadly applicable for establishing immortalized epithelial cell lines from primary human tissues for cancer research.
The evolution of cancer cells involves the acquisition of mutations that often fall within a set of defined genetic pathways. Experimental transformation of normal human cells into cancer cells through the introduction of defined oncogenic lesions represents a major breakthrough in cancer research, as this approach enables the step-by-step re-construction of the oncogenic process. It has been established that multiple alterations are required to transition primary human epithelial cells to a neoplastic/cancerous state in vitro. Primary human cells cultured in vitro experience two proliferation blockades, senescence and crisis . When grown in chemically defined media without feeder cells, primary human epithelial cells undergo rapid senescence that is likely a result of cell culture stress . Cell culture senescence is associated with the up-regulation of the tumor suppressor p16INK4A and the subsequent activation of the Rb protein. Senescence can be bypassed with expression of viral oncoproteins that neutralize Rb and p53 activity [3–5]. These include the SV40 polyomavirus Large T (LgT) antigen [6, 7], the adenovirus E1A protein [1, 3, 5, 8], and the papillomavirus E6 and E7 proteins [2, 6, 9–11]. Human cells that have by-passed senescence still have limited replicative potential due to insufficient telomerase activity, and they eventually encounter crisis due to progressively shortening telomeres [1, 12, 13]. Re-expression of the catalytic subunit of telomerase, hTERT, which is sufficient to restore telomerase activity in many cell types [2, 14], can prevent telomere erosion, maintain genomic stability and immortalize cells [3–5, 15–18]. Historically, primary human cells have been immortalized through a two-step process: the first step involves the introduction of the aforementioned viral oncoproteins to neutralize Rb and p53 activity to bypass cell culture senescence [4, 6, 7]. The second step involves the introduction of hTERT, which serves to maintain telomere stability and prevent crisis . Primary human epithelial cells immortalized this way can be successfully transformed by oncogenes such as Ras [19, 20]. This step-wise approach provides a valuable means to model malignant transformation under genetically defined conditions. Since most human cancer cells do not harbor viral oncoprotein expression, recent studies have sought to obviate the need for viral oncoproteins. It has been shown that the over-expression of the G1 cell cycle kinase CDK4 [21, 22] or shRNA-mediated knockdown of p16INK4A [23, 24] can immortalize cells in the presence of hTERT.
Lung cancer is a leading cause of cancer-related mortality in the United States and worldwide. Approximately ~80% of lung cancer are non-small cell lung cancer (NSCLC) that is thought to originate from epithelial cells of the small airway or the alveolus [25–27]. Sequencing studies and copy number variation analyses have revealed that human lung adenocarcinomas frequently harbor mutations in KRAS, TP53 and CDKN2A [28, 29]. Previously, several studies have showed that NSCLC can be modeled in vitro with human airway and bronchial epithelial cells [20, 30, 31]. In these studies, primary airway and bronchial epithelial cells were immortalized using hTERT together with either viral oncoproteins  or CDK4 overexpression . Subsequent introduction of oncogenes such as KRAS could transform these cells and enable tumor growth in vivo [20, 30, 31].
Here we developed a simplified, one-step immortalization method for primary human cells and we demonstrated its utility in immortalizing human small airway epithelial cells (SAECs). We showed that immortalized SAECs are chromosomally stable and can be transformed by the KRAS oncogene in vitro. This approach should facilitate the establishment of isogenic panels of normal and transformed human cell lines for the study of malignant transformation.
One-step immortalization of small airway epithelial cells
To validate our one-step immortalization approach, we engineered additional constructs that expressed a negative control shRNA targeting firefly luciferase (sh_ctrl) instead of sh_p16, and constructs that expressed the enhanced green fluorescent protein (EGFP) instead of hTERT. We transduced primary SAECs with these constructs and generated stable, polyclonal cell lines following drug selection. In the untransduced cells, p16INK4A protein was expressed at moderate levels, whereas p14ARF protein was expressed at very low levels (Fig. 1b, lane 1). Since our sh_p16 targets a common exon shared by both p16INK4A and p14ARF, it knocked down both proteins by western blot (Fig. 1b, lanes 4, 5). To verify the activity of the hTERT cDNA, we used a PCR-based telomeric repeat amplification protocol (TRAP) assay to confirm that telomerase activity was indeed elevated in cells expressing hTERT but not in cell expressing EGFP (Fig. 1c).
iSAEC morphology and genomic stability
Morphologically, iSAECs at early passage 19 (P19) and late passage (P71) exhibit similar features under phase-contrast microscopy (Fig. 2b). In contrast to BJ fibroblasts, iSAECs expressed the epithelial marker keratin-19, similar to the NSCLC cell line HCC4006 (Fig. 2c). Western blots showed that iSAECs expressed the epithelial marker E-cadherin, although they also expressed the mesenchymal marker vimentin at a low level (Fig. 2d). Thus we concluded that iSAECs have largely retained their epithelial characteristics throughout the immortalization process.
Oncogenic transformation of iSAECs by mutant KRAS
Lastly, we wished to determine how iSAECs would respond to oncogenic transformation by the KRAS oncogene. We generated iSAECs stably expressing HA-tagged WT KRAS protein (KRASWT) or the constitutively active mutant KRAS-G12V protein (KRASV12) under the control of a tetracycline (tet)-inducible promoter. In these cells, doxycycline treatment leads to a dose-dependent induction of HA-KRAS (Fig. 4b). Unexpectedly, induction of KRASV12 did not dramatically activate the MAPK pathway as measured by ERK kinase phosphorylation (Fig. 4b). Neither was this level of KRASV12 expression able to confer anchorage-independent grow in soft agarose. We next used a tet-inducible EGFP-KRASV12 fusion construct which can be expressed at a higher level to elevate phospho-ERK level (Fig. 4c). Under these conditions the mutant EGFP-KRASV12 protein enabled AI colony formation (Fig. 4d). However, the clonogenic efficiency was low and only ~0.5% of cells formed soft agarose colonies. Thus, iSAECs are capable of being transformed by the KRAS oncogene at a low efficiency, and it is likely that additional genetic perturbations are required for their full transformation .
In this study, we developed a method that enables the one-step immortalization of human primary epithelial cells through the simultaneous introduction of hTERT cDNA and a shRNA against the CDKN2A locus. We demonstrate that this approach led to the establishment of immortalized cells capable of replication beyond the Hayflick limit  while maintaining telomeres and genomic stability.
We avoided using viral oncoproteins such as LgT, E6 and E7 in our approach as these proteins inactivate both the Rb and p53 pathway. We demonstrate that p16INK4A knockdown in combination with hTERT was sufficient for cell immortalization, similar to a previous report . Due to the shared exon usage between p16INK4A and p14ARF proteins, we were unable to identify a potent shRNA that selectively knockdown p16INK4A but not p14ARF. However, in the case of SAECs, p14ARF expression level was very low and its depletion did not lead to loss of p53 proteins. Indeed, we found that in proliferating iSAECs p53 was expressed and could be readily activated by DNA damage. Thus, p53 function is at least partially preserved in iSAECs and full p53 inactivation may not be an obligatory requirement for the immortalization of these cells [21, 24]. Interestingly, in iSAECs, total p53 protein level was not substantially elevated by DNA damage. This was unexpected as phosphorylation typically stabilizes p53 by interfering with its binding to the E3 ligase MDM2 . Whether this phenomenon is specific to SAECs or is associated with our particular method of cell immortalization require further investigation. Nevertheless, our approach allows p53 activity to be manipulated separately, as we demonstrated with shRNA mediated p53 knockdown. This is a useful feature as it enables the study of genetic interaction between p53 and other oncogene and tumor suppressors in this model system.
In iSAECs, the introduction of the KRAS oncogene could drive soft-agarose colony growth. However, the transformation efficiency was low and it required relatively high levels of KRAS expression. Our findings thus indicate that human airway epithelial cells are relatively resistant to malignant transformation elicited by a single oncogene. This is in agreement with previous studies indicating that KRAS alone was unable to fully transform immortalized airway epithelial cells and cooperation from additional oncogenes including PIK3CA and MYC are necessary for their full transformation [20, 22, 31].
A convenient method to immortalize cells serves two valuable purposes. First, immortalized cells such as iSAECs provide a starting point for the evaluation of oncogene and tumor suppressor function in a prospective, isogenic setting. This enables step-wise reconstruction of the oncogenic process by the introduction of defined genetic changes [19, 20, 22, 30, 31]. Second, immortalized but non-transformed epithelial cells are valuable “normal” controls for tumor cell lines for evaluating drug target and drug candidate toxicity. Currently, many human cancer cell lines lack “normal” counterparts from the same tissue. Although we only tested SAECs in this study, it is likely that, with the appropriate media conditions, our approach should facilitate the creation of immortalized epithelial cell lines from various tissues for cancer research.
Cell culture and pharmacological agents
Primary human small airway epithelial cells were purchased from Lonza. Cells were cultured in SAGM growth media (Lonza). BJ Fibroblasts (ATCC) were cultured in eagle’s minimum essential medium (ATCC) supplemented with 10% heat inactivated fetal bovine serum (Hi-FBS, Life Technologies) and 100 units/mL penicillin plus 100 µg/ml streptomycin (P/S, Lonza). U2OS cells were cultured in McCoy’s 5A Media (Lonza) supplemented with 10% Hi-FBS and P/S. Cells were maintained at 37 °C in 5% CO2. Doxorubicin was used at a concentration of 200 nM for cell culture treatment. KaryoMAX® Colcemid™ Solution in PBS (Life Technologies) was used at a concentration of 0.1 ug/mL for metaphase spreads. Doxycycline was from Sigma.
Plasmid construction and generation of stable cell lines
MSCV-pic2 is a retroviral vector that co-expresses a cDNA and a shRNA. For one-step immortalization, we introduced into this vector the cDNA of the catalytic subunit of hTERT and a shRNA for the CDKN2A gene locus that knocks down both p16INK4A and p14ARF. Plasmids generated using the MSCV-pic2 vectors include: MSCV-pic2-neo-hTERT-sh_p16, MSCV-pic2-neo-EGFP-sh_p16, MSCV-pic2-neo-hTERT-sh_Ctrl, MSCV-pic2-neo-EGFP-sh_Ctrl. The shRNA target sequences were: sh_p16 (ACTCGGGAAACTTAGATCATCA), sh_p53 (CCCGGCGCACAGAGGAAGAGAA), sh_Ctrl (firefly luciferase shRNA CCCGCCTGAAGTCTCTGATTAA). The lentiviral tet-inducible vectors expressing EGFP-KRAS V12 and WT proteins were described before . Plasmids were packaged in 293T cells with Trans-IT-293 Transfection Reagent (Mirus Bio). SAECs were transduced by spin infection at 1800 RPM for 45 min. Stable cell lines were generated using the drug selectable markers associated with each vector.
Cells were lysed directly with Laemmli sample buffer. Whole cell lysates were boiled for 10 min at 95 °C and subsequently stored at −80 °C. Whole cell lysates were separated using BioRad Mini-Protean TGX 4–20% resolving gels. The protein was then transferred to a nitrocellulose membrane. The source of antibodies were: p16INK4A (BD Bioscience #551153), p14ARF (Bethyl, A300-340A), p53 (Santa Cruz #DO-1 SC-126), p21 (Calbiochem #OP64) Vinculin (Sigma #V9131), GAPDH (Santa Cruz #SC-25778) and phospho-p53-S15 (Cell Signaling Technology #9284), KRAS (Sigma, clone 4F3), phospho-ERK (Cell Signaling Technology, #4377), total ERK (Cell Signaling Technology, #9102), phospho-Akt (Cell Signaling Technology, #4058), Akt (Cell Signaling Technology, #9272), E-Cadherin (Cell Signaling Technology, #24E10), N-Cadherin (Cell Signaling Technology, #13116), Vimentin (Cell Signaling Technology, #5741). Blots were developed using conjugated anti-rabbit or anti-mouse and either Luminata Forte (Millipore) substrate or SuperSignal West Femto (Pierce) substrate on an Alpha Innotech HD2 Western Blot Imaging Station (protein Simple). Images were quantified with Alpha Innotech Image Software or Adobe Photoshop. Cropping and contrast adjustment were applied to entire images consistently without local alterations.
Quantitative reverse transcription PCR
RNA was extracted from early and late passage iSAECs, BJ Fibroblasts, and HCC4006 NSCLC cell line using the RNA easy Kit and QiaShredder Columns (Qiagen). Collected RNA was reverse transcribed to cDNA using Multiscribe Reverse Transcriptase (Applied Biosystems). Real-time PCR was performed on the ABI 79300HT Real-Time Thermo Cycler with SYBR Green using the following primers pairs: KRT19_F (ACCAAGTTTGAGACGGAACAG) and KRT19_R (CCCTCAGCGTACTGATTTCC), B-Actin_F (AGAGCTACGAGCTGCCTGAC) and B-Actin_R (AGCACTGTGTTGGCGTACAG). All mRNA levels were normalized to B-Actin levels and KRT19 levels in BJ Foreskin Fibroblasts. mRNA levels are the average of three technical replicates, and error bars are standard deviation.
Cell cycle analysis flow sorting
Log phase iSAEC passage 19 (P19) and iSAEC (P71) were collected, stained and fixed with propidium iodide (Sigma-Aldrich). Cells were scanned with a FACS Calibur analyzer (Beckson-Dickinson) and the data acquired with CellQuest Pro software. FACS profiles were analyzed using ModFit LT for all samples. The experiment was performed with three biological replicates of iSAECs.
Metaphase spreads, FISH, and microscopy
Log-phase, iSAEC (P14), iSAEC (P79) and BJ Fibroblasts (P18) were treated with KaryoMAX® Colcemid™ Solution in PBS at 0.1 ug/mL for 6 h at 37 °C. Mitotic fractions of cells were collected and pre-warmed 75 mM hypotonic solution was added to the mixture and incubated at 37 °C for 25 min. Mitotic cells were fixed in a solution of 3:1 v/v Methanol to Acetic Acid. Slides were prepared and stained with SlowFade® Gold Antifade Mountant with DAPI (Life Technologies). Metaphase spreads were imaged with Zeiss Axio Microscope on a 63× Oil Objective. Metaphase spreads were quantified manually using Adobe Photoshop for labeling and isolation of chromosomes. Metaphase spreads of iSAEC (P61) were prepared as described above. Before the addition of DAPI, slides were stained with Telomere PNA Cy3 probe (DAKO) according to the manufacturer’s instructions and then cross-stained with SlowFade® Gold Antifade Mountant with DAPI. Telomere probe slides were imaged with Zeiss Axio Imager on a 63× Oil Objective.
Telomerase activity was quantified using the TRAPEZE RT Telomerase Detection Kit (Millipore) according to the manufacturer’s instructions.
Anchorage independent growth assays
Cells were plated at 5000 cells/well in 6-well plates in triplicates in soft-agarose. For tet-inducible EGFP-KRAS expression, doxycycline (100 ng/ml) was included in both the agarose-media mix. Cells were allowed to grow for 16 days. Colonies were stained with 0.005% crystal violet in 5:4:1 methanol: water: acetic acid. Colonies were quantified using the Alpha Innotech Imaging Station Colony Counter Software.
Stably transduced SAEC-hTERT-sh_p16, SAEC-GFP-sh_p16, SAEC-GFP-FF2, and untransduced SAECs were seeded in a 6-well plate and continuously passaged in log-phase for approximately 90 days. Media was changed every other day, and population doubling was measured every three to four days when confluency reached 80–90%.
enhanced green fluorescent protein
non-small cell lung cancer
small airway epithelial cells
telomeric repeat amplification protocol
JLS, LCL and JL conceived and designed the study; JLS, LCL, AR, QL, BY and CSL carried out experiments; JLS, LCL, AR and JL wrote the manuscript. All authors read and approved the final manuscript.
We thank Dr. J. Silvio Gutkind for technical suggestions and Dr. Anna V. Roschke for assistance with metaphase spread analysis.
The authors declare that they have no competing interests.
Data availability statement
Data sharing not applicable to this article as no datasets were generated or analysed during the current study.
This work was supported by a NCI Intramural Award ZIA BC 011304 to JL.
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