Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Here we describe a time-specific method to effectively manipulate critical developmental pathways in the mouse placenta in vivo. This is performed through the injection and electroporation of CRISPR plasmids into the placentas of pregnant dams on embryonic day 12.5.

Abstract

The placenta is an essential organ that regulates and maintains mammalian development in utero. The placenta is responsible for the transfer of nutrients and waste between the mother and fetus and the production and delivery of growth factors and hormones. Placental genetic manipulations in mice are critical for understanding the placenta's specific role in prenatal development. Placental-specific Cre-expressing transgenic mice have varying effectiveness, and other methods for placental gene manipulation can be useful alternatives. This paper describes a technique to directly alter placental gene expression using CRISPR gene manipulation, which can be used to modify the expression of targeted genes. Using a relatively advanced surgical approach, pregnant dams undergo a laparotomy on embryonic day 12.5 (E12.5), and a CRISPR plasmid is delivered by a glass micropipette into the individual placentas. The plasmid is immediately electroporated after each injection. After dam recovery, the placentas and embryos can continue development until assessment at a later time point. The evaluation of the placenta and offspring after the use of this technique can determine the role of time-specific placental function in development. This type of manipulation will allow for a better understanding of how placental genetics and function impact fetal growth and development in multiple disease contexts.

Introduction

The placenta is an essential organ involved in the development of the fetus. The main role of the placenta is to provide essential factors and regulate the transfer of nutrients and waste to and from the fetus. Mammalian placentas are composed of both fetal and maternal tissue, which make up the fetal-maternal interface, and, thus, the genetics of both the mother and fetus impact function1. Genetic anomalies or impaired function of the placenta can drastically alter fetal development. Previous work has shown that placental genetics and development are associated with the altered development of specific organ systems in the fetus. Particularly, ....

Protocol

All procedures were performed in accordance and compliance with federal regulations and University of Iowa policy and were approved by Institutional Animal Care and Use Committee.

1. Animals and husbandry

  1. Keep the animals in a 12 h daylight cycle with food and water ad libitum.
  2. Use CD-1 female mice aged 8-15 weeks. Use the presence of a copulatory plug to identify E0.5.
  3. On E0.5, singly house the pregnant dams.

Representative Results

General procedure outcomes (Figure 6)
In the study, there were three manipulated groups. These included placentas injected with a general CRISPR Cas9 control plasmid (Cas9 Control), an activation control CRISPR plasmid (Act Control), or an IGF-1 SAM activation plasmid (Igf1-OE). The Cas9 Control is better suited for knockout plasmids, and the activation control is better suited for overexpression/activation plasmids. To assess the viability ch.......

Discussion

The placenta is a primary regulator of fetal growth, and as previously noted, changes in placental gene expression or function may significantly impact fetal development6. The protocol outlined here can be used to perform a targeted in vivo CRISPR manipulation of the mouse placenta using a relatively advanced surgical approach. This technique allows for a significant yield of viable embryos and their corresponding placentas that can be used for further study (Figure 6.......

Acknowledgements

The authors acknowledge the following funding sources: R01 MH122435, NIH T32GM008629, and NIH T32GM145441. The authors thank Dr. Val Sheffield and Dr. Calvin Carter's labs at the University of Iowa for the use of their surgery room and equipment, as well Dr. Eric Van Otterloo, Dr. Nandakumar Narayanan, and Dr. Matthew Weber for their assistance with microscopy. The authors also thank Dr. Sara Maurer, Maya Evans, and Sreelekha Kundu for their assistance with the pilot surgeries.

....

Materials

NameCompanyCatalog NumberComments
1.5 ml TubesUSA Scientific Inc1615-5500
4% Paraformeldhyde (PFA) in PBSThermo Fisher ScientificJ61899.AP
96 Well plateCornings3598For BCA kit
Absorbent UnderpadsFisher Scientific14-206-62
Activation Control PlasmidSanta Cruz Biotechnologysc-437275Dnase-free water provided for dilution
AMV Reverse TranscriptaseNew England BiolabsM0277LUse for cDNA synthesis
Anesthetic Gas VaporizorVetamacVAD-601TTVAD-compact vaporizer
Artifical Tear GelAkornNDC 59399-162-35
BCA Protein Assay KitThermo Fisher Scientific23227Protein quantification
BiovortexerBellco Glass, Inc.198050000Hand-held tissue homogenizer
CellSens SoftwareOlympusV4.1.1Image processing to FISH images.
Centrifuge 5810EppendorfEP022628168Plate centrifuge
ChloroformThermo Fisher ScientificJ67241-APRNA isolation
Cotton Tipped ApplicatorsProAdvantage77100Sterilize before use
CRISPR/Cas9 Control PlasmidSanta Cruz Biotechnologysc-418922Dnase-free water provided for dilution
CryoStatLeicaCM1950
Dissection MicroscopeLeicaM125 CUsed for post-necroscopy imaging
Dissolvable SuturesMed Vet InternationalJ385H
Distilled WaterGibco15230162
Dulbecco's Phosphate Buffered Saline (DPBS)Thermo fisher Scientific14190144(-) Calcium; (-) Magnesium
ECM 830 Electro Electroporator (Electroporation Machine)BTX Harvard Apparatus45-0662Generator only
Electric RazorWahlCL9990Kent Scientific
Electroporation paddles/TweezertrodesBTX Harvard Apparatus45-04873 mm diameter paddles; wires included
Embedding Cassette: 250 PKGrainger21RK94Placenta embedding cassettes
EthanolThermo Fisher Scientific268280010
F-Air CanistersPenn Veterinary Supply IncBIC80120Excess isoflurane filter
Fast Green Dye FCFSigmaF7252-5GDissolve to 1 μg/ml and filter; protect from light
Filter-based microplate photometer (plate reader)Fisher Scientific14377576Can be used for BCA and ELISA
ForcepsVWR82027-386Fine tips, straight, serrated
Formalin solution, neutral buffered, 10%Sigma AldrichHT501128
Glass Capillaries - Borosilicate Glass (Micropipette)Sutter InstrumentB150-86-10O.D.: 1.5 mm, I.D.: 0.86 mm, 10 cm length
Halt Protease and Phosphotase inhibitor cocktail (100x)Thermo Scientific1861281Protein homogenization buffer
Heating PadThermotechS766DDigitial Moist Heating Pad
HemostatsVWR10806-188Fully surrated jaw; curved
Hot Water BathFisher Scientific20253Isotemp 205
Igf-1 SAM Plasmid (m1)Santa Cruz Biotechnologysc-421056-ACTDnase-free water provided for dilution
Induction ChamberVetamac941443No specific liter size required
IsofluranePiramal Pharma LimitedNDC 66794-013-25
Isoproponal/2-ProponalFisher ScientificA451-4RNA isolation
Ketamine HCl 100mg/mlAkornNDC 59399-114-10
MgCl2/Magneisum ChlorideSigma Aldrich63069-100ML1M. Protein homogenization buffer
MicroAmpâ„¢ Optical 384-Well Reaction Plate with BarcodeFisher Scientific4309849Barcoded plates not required
Microcapillary TipEppendorf5196082001Attached to BTX Microinjector
MicroinjectorBTX Harvard Apparatus45-0766Stainless Steel Pipette Holder, 130 mm Length, for 1 to 1.5 mm Pipettes
Microject 1000A (Injection Machine)BTX Harvard Apparatus45-0751MicroJect 1000A Plus System
Micropipette Puller Model P-97Sutter InstrumentP-97Flaming/Brown type micropipette puller
Microplate Mixer (Plate Shaker)scilogex822000049999
Mouse/Rat IGF-I/IGF-1 Quantikine ELISA KitR & D SystemsMG100
NeedlesBD - Becton, Dickson, and Company30510630 Gx 1/2 (0.3 mm x 13 mm)
Nitrogen TankLinde7727-37-9Any innert gas
Non-Steroidal Anti-Inflammatory Drug (NSAID)Norbrook Laboratories LimitedNDC 55529-040-10Analesgic such as Meloxicam
Nose ConeVetamac9216099-14 mm
Opal 620 detection dyeAkoya BiosciencesSKU FP1495001KTUsed for FISH
Optimal Cutting Temperature (O.C.T) CompoundSakura4583
Oxygen TankLinde7782 - 44 - 7Medical grade oxygen
PestlesUSA Scientific Inc14155390
Povidone-Iodine Solution, 5%Avrio Health L.P.NDC 67618-155-16
Power SYBRâ„¢ Green PCR Master MixThermo Fisher Scientific4367659Use for qPCR
Random Hexamers (Random Primers)New England BiolabsS1330SUse for cDNA synthesis
Razor BladeGrainger26X080
RNA Cleanup Kit & ConcentratorZymo ResearchR1013
RNALaterThermo Fisher ScientificAM7021
RNAscope kit v.2.5Advanced Cells Diagnostics323100Contains all reagents required for fluorescent in situ hybridization. Probes sold separately.
RNAscope™ Probe- Mm-Prl8a8-C2Advanced Cells Diagnostics 528641-C2
RNAscopeâ„¢ Probe- Vector-dCas9-3xNLS-VP64Advanced Cells Diagnostics527421
Roto-Therm MiniBenchmarkR2020Dry oven for in situ hybridization
ScissorsVWR82027-578Dissecting Scissors, Sharp Tip, 4¹/₂
Sodium Chloride (Saline)HospraNDC 0409-4888-03Sterile,  0.9%
Sodium Citrate, Trisodium Salt, Dihydrate, [Citric Acid, Trisodium Dihydrate]Research Product International03-04-6132
Sodium Hydroxide 1N Concentrate, Fisher ChemicalFisher ScientificSS277Protein homogenization buffer
SteamerBellaB00DPX8UBA
Sterile Surgical DrapeBusse696Sterilize before use
Superfrost Plus Microscope SlidesFisher Scientific12-550-15
Surgipath Cover Glass 24x60Leica3800160
SyringesBD - Becton, Dickson, and Company309659BD Luer Slip Tip Syringe sterile, single use, 1 mL
Thermo Scientific™ Invitrogen™ Nanodrop™ One Spectrophotometer with WiFi and Qubit™ 4 FluorometerFisher Scientific13-400-525This configuration comes with Qubit 4 fluorometer.  Qubit quantification not required.
Tissue Adhesive3M1469SBVetBond
Tris HClThermo Fisher Scientific155680251M. Protein homogenization buffer
TRIzolâ„¢ ReagentThermo Fisher Scientific15596018RNA isolation
TSA Buffer PackAdvanced Cells Diagnostics322810Used to dilute Opal 620 detection dye
Universal F-CircuitVetamac40200Attached to vaporizer and vaporizer accessories
Upright Compound Fluorescence MicroscopeOlympusBX61VSUsed for FISH imaging
Vectorshield with DAPIVector LaboratoriesH-1200Coverslip mounting media
ViiA™ 7 Real-Time PCR System with 384-Well BlockThermo Fisher Scientific4453536This is for SYBR 384-well block detection.  TaqMan and/or smaller blocks available
Wet n Wild Nail Polish Wild Shine, Clear Nail Protector, Nail ColorAmazonC450B
Xylazine 20mg/mlAnased343730_RX

References

  1. Cross, J. C., et al. Genes, development and evolution of the placenta. Placenta. 24 (2-3), 123-130 (2003).
  2. Perez-Garcia, V., et al. Placentation defects are highly prevalent in embryonic lethal mouse mutants.

Explore More Articles

MousePlacentaCRISPRGenetic ManipulationIn VivoTargetedMid late PregnancyOverexpressionAnesthesiaLaparotomyUterine HornPlacental InjectionElectroporation

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved