Mouse Round Spermatid Injection

Summary

Here, we introduce a method for performing round spermatid injection (ROSI) in mice, a technique with promising clinical applications and utility for investigating the mechanisms underlying embryonic development.

Abstract

Round spermatids, characterized by their haploid genetic content, represent the precursor cells to mature spermatozoa. Through the innovative technique of round spermatid injection (ROSI), oocytes can be successfully fertilized and developed into viable fetuses. In a groundbreaking milestone achieved in 1995, the first mouse fetus was born through ROSI technology. ROSI has since emerged as a pivotal tool for unraveling the intricate mechanisms governing embryonic development and holds significant potential in various applications, including the acceleration of mouse generation and the production of genetically modified mice. In 1996, a milestone was reached when the first human fetus was born through ROSI technology. However, the clinical applications of this method have shown a fluctuating pattern of success and failure. To date, ROSI technology has not found widespread application in clinical practice, primarily due to its low birth efficiency and insufficient validation of fetal safety. This article provides a comprehensive account of the precise methods of performing ROSI in mice, aiming to shed new light on basic research and its potential clinical applications.

Introduction

The final stage of spermatogenesis involves the transformation of a round spermatid into a fully developed spermatozoon, characterized by distinct head, neck, and elongated tail structures¹. This transformation encompasses significant changes in cell morphology, such as the condensation of chromatin in the nucleus, replacement of histones by protamine, acrosome formation, mitochondrial sheath development, centriole migration and loss, tail structure formation, and the removal of cellular residues².

In 1992, the first human fetus was successfully born through intracytoplasmic sperm injection (ICSI) technology³. Since then, researchers have been exploring the potential of utilizing round spermatids, which share the same haploid genetic composition as mature spermatozoa, to fertilize oocytes and sustain viable pregnancies^2,4. Subsequently, in 1996, the first human fetus conceived via round spermatid injection (ROSI) technology was delivered^5,6. It is worth noting that studies involving ICSI and ROSI in mice lagged behind those in humans due to the susceptibility of the mouse oocyte membrane to damage during the injection process. This issue was successfully resolved with the introduction of the Piezo membrane-breaking device. Consequently, in 1995, the first mouse conceived through ROSI technology was born. Additionally, research on ROSI in various other animals is also underway^7,8.

Currently, research on ROSI primarily centers around the following aspects: clinical application, mechanism elucidation, and strategies to enhance developmental efficiency, along with broader applications of ROSI technology. In the context of clinical applications, despite the birth of the first ROSI human fetus through ROSI in 1996, progress has been marked by a series of successes and failures^9,10,11,12. To date, ROSI technology has not achieved widespread clinical implementation, largely due to its low efficiency and the need for further validation regarding the safety of fetuses conceived through ROSI technology. Incomplete statistics indicate that globally, fewer than 200 human ROSI-conceived fetuses have been delivered. A turning point in understanding the potential of ROSI technology occurred in 2015 when Tanaka and colleagues reported on the successful birth of 14 fetuses through ROSI technology, instilling renewed confidence in its clinical application and feasibility^13,14. ROSI technology holds substantial promise for addressing reproductive biology challenges, particularly in non-obstructive azoospermia patients. In addition to its clinical applications, ROSI serves as a valuable tool for studying the intricate mechanisms of embryonic development^15,16,17.

Numerous animal studies have been conducted to investigate the underlying factors contributing to the low efficiency of ROSI in achieving full embryonic development. These factors encompass the choice of assisted oocyte activation (AOA) methods and their timings, abnormalities in genomic stability, and, particularly, abnormalities in epigenetic modifications. It is important to recognize that round spermatids are immature germ cells, differing significantly from mature spermatozoa in various physiological aspects. Mizuki Sakamoto and colleagues indicated that H3K27me3, derived from round spermatids, is associated with chromatin that is less accessible and leads to impaired gene expression in ROSI embryos¹⁸. In a related study by Jing Wang and colleagues, reprogramming defects in ROSI embryos at the pronuclear stages were predominantly associated with the misexpression of a cohort of the genes responsible for minor zygotic genome activation¹⁹. They also found that introducing a selective euchromatic histone lysine methyltransferase 2 inhibitor, A366, could potentially enhance the overall developmental rate by approximately twofold.

The mouse stands as one of the most valuable model animals for studying embryonic development. This article elaborates on how to perform ROSI on mice. This comprehensive protocol encompasses the selection of suitable mice, detailed ovulation induction procedures, AOA techniques, injection techniques, and the preparation of surrogate mice. Furthermore, we present a comparative analysis of the effects of two injection regimens on birth efficiency: AOA followed by ROSI (A-ROSI; first regimen) and ROSI followed by AOA (ROSI-A; second regimen). We aim to encourage researchers to conduct mouse ROSI experiments with greater precision, offering more robust support for their clinical application and the fundamental research of embryonic development mechanisms.

Protocol

B6D2F1 (C57BL/6 x DBA/2), C57BL/6, and ICR mice used in this experiment were purchased from Beijing Vital River Laboratory Animal Technologies Co. Ltd. (Beijing, China). All animal treatments adhered to the experimental procedures and standards approved by the Experimental Animal Ethics Committee of the First Hospital of Jilin University (approval number: 20200435).

1. Preparation of relevant reagents

1. Acquire some reagents commercially and self-prepare the remaining reagents.
   1. Obtain M₂, a buffer system for in vitro processing of round spermatids (RS), spermatozoa, and oocytes from the supplier.
   2. Prepare the Ca²⁺-free C.L. Chatot, C.A. Ziomek, and B.D. Bavister (CZB) medium for AOA following the previously published protocol²⁰.
   3. Obtain the potassium simplex optimized medium supplemented with amino acids (KSOMaa) solution for embryo culture from the supplier.
   4. Prepare hyaluronidase, with a working concentration of 0.1% (1 g/L), by dissolving 0.1 g of hyaluronidase in 1 mL of embryo water. Take 10 µL of concentrated storage solution and dissolve in 990 mL of M₂, which could be stored at 4 °C for 1 week.
   5. Prepare polyvinylpyrrolidone (PVP), with an average molecular weight of 360,000 and a mass concentration of 12%, by dissolving 1.2 g of PVP in 10 mL of M₂. The resulting solution could be stored at 4 °C for 1 week.
   6. Store the cytochalasin B (CB) stock solution (2 µL), soluble in 18 µL of DMSO at -20 °C. Take 5 µL of the concentrated storage solution and dissolve in 995 mL of M₂. The resulting solution could be stored at 4 °C for 1 week.

2. Preparation of oocytes

1. Acclimate female B6D2F1 mice, aged 6-8 weeks, to their new environment for at least 1 week. Inject intraperitoneally with 7.5 IU of pregnant mare serum gonadotropin (PMSG) at 5 pm, followed by 7.5 IU of human chorionic gonadotropin (HCG) 48 h later. Ensure no contact with male mice occurs after the injection.
2. After 14 h of HCG injection, euthanize the mice using the cervical dislocation method. Open the abdominal cavity and locate the uterus. Identify the ovaries along the uterus and sever the fallopian tubes near the ovaries using scissors. Repeat the same procedure on the other side and place the fallopian tubes in M₂, which is preheated at 37 °C in advance.
3. Under an upright microscope (10x), locate the enlarged part of the fallopian tube, showing a transparent and swollen appearance. Use a 1 mL syringe to secure the fallopian tube while cutting the enlarged part, collecting oocyte coronal cumulus complexes (OCCCs).
4. Place OCCCs into the preheated M₂ operating solution containing 0.1% hyaluronidase and remove granulosa cells by gently blowing through an oral pipette.
   NOTE: Keep the OCCCs in 0.1% hyaluronidase for a short duration, approximately 2 min, if needed.
5. After removing the granulosa cells, transfer the oocyte to KSOMaa, rinse 3x, and place in a carbon dioxide incubator for later use (37 °C, 5% CO₂).

3. Preparation of round spermatids and spermatozoa

1. Collect round spermatids and spermatozoa from the testis and epididymis of male C57BL/6 mice (8-10 weeks), respectively.
   1. For spermatozoa, euthanize the mice by cervical dislocation. Open the abdominal cavity, locate the epididymis near the testis, and gently excise with scissors.
   2. Place the epididymis in M₂ medium and gently excise using a 1 mL syringe to allow spermatozoa to flow out under an upright microscope (10x).
   3. Siphon the flowing spermatozoa and M₂ suspension into the bottom of a tube containing 0.5 mL of M₂, allowing the spermatozoa to flow upstream naturally. Set them aside for later use.
   4. For round spermatids, remove the testicles from the abdominal cavity and place them in M₂. Gently cut the white membrane through using a 1 mL syringe and squeeze the convoluted seminiferous tubules out under an upright microscope (10x).
   5. Excise the seminiferous tubules carefully using two 1 mL syringes. Extract the suspension and filter with a 400-mesh sieve (38 µm).
2. Centrifuge the filtered cells, discard the supernatant, and add 200 µL of Hoechst 33342 for staining, followed by incubation at 37 °C for 10 min.
3. Perform fluorescence-activated cell sorting (FACS) to distinguish round spermatids from other cell types. Place the stained cells into a flow cytometry tube and perform a round spermatid screening.
   1. Different models of flow cytometry machines have different regulatory parameters and can be communicated with technical support during operation. As the first step, adjust the voltage and select the cell population according to forward scatter (FSS) and side scatter (SSC; see Supplementary Table 1).
   2. For the second step, remove cell adhesions according to FSC and trigger pulse width.
   3. As the third step, select the target haploid round spermatids. Hoechst 33342 binds to DNA, and cells with different ploidy exhibit different fluorescence intensities. Set the excitation wavelength to 355. Select two detection channels, 460/50 and 670/30, under 355 wavelength laser to sort round spermatids. Subsequently, store the sorted round spermatids in a 4 °C refrigerator for later use.
      NOTE: It is also possible to directly select round spermatids based on their morphology under a microscope, but training is required to ensure selection accuracy.

4. Round spermatid injection (ROSI)

1. Carry out the ROSI procedure using an inverted microscope with a micromanipulation system.
2. In the initial preparation step, make holding and injection needles according to the previously described procedure²¹. Keep the inner diameter of the injection needle between 6-7 µm, designed for the extraction of round spermatids, and for the holding needle, have an inner diameter of 20 µm for securing the oocyte.
3. In the subsequent preparation step, create an injection vessel by placing 10 µL of M₂ droplets containing CB to soften oocytes and 10 µL of M₂ droplets for storing round spermatids. Use PVP droplets to moisten and cleanse the injection needles.
   NOTE: Adding CB here is not a necessary step, but adding CB can greatly improve the survival rate after injection.
4. Extract round spermatids using an injection needle.
5. Rotate the oocyte with a holding needle, positioning the oocyte's polar body at either the 12 o'clock or 6 o'clock position.
6. Place the injection needle carefully at the 3 o'clock position on the oocyte, tightly adhering to the zona pellucida. Use a PiezoXpert device to create a hole in the zona pellucida. Adjust the strength from small to large, which is approximately intensity = 5 and speed = 15 here.
7. Gently advance the injection needle through the zona pellucida and enter the oocyte horizontally. When it passes the center of the oocyte, apply a piezo (intensity = 1 and speed = 1), resulting in the rupture of the oocyte membrane and the gradual injection of the round spermatid into the oocyte's cytoplasm.
8. Withdraw the injection needle and aspirate a small amount of the oocyte's membrane near the opening to seal it. This step is crucial, as failure to seal would result in cytoplasmic leakage and oocyte death.
   NOTE: It is worth noting that ROSI required AOA either before or after the injection of round spermatids, which we have discussed in subsequent sections.

5. Intracytoplasmic sperm injection (ICSI)

1. Carry out the same steps for ICSI as for ROSI, with the only difference being the diameter of the ICSI injection needle, which measures 9-10 µm.
2. Place spermatozoa on a PVP runway to reduce their swimming speed and facilitate sperm extraction.
3. Perform separation of the spermatozoa head and tail for ICSI. Aspirate the spermatozoa from the tail and position the spermatozoa's neck precisely at the mouth of the injection needle. Apply a piezo (multiple piezo could be used as needed, intensity = 5 and speed = 15) to separate the head and tail of the spermatozoa.

6. Assisted oocyte activation (AOA)

1. According to the protocol, prepare a CZB medium without calcium and magnesium.
2. Use strontium chloride hexahydrate (SrCl₂6H₂O), with a molecular weight of 266.62, at a concentration of 10 mM. To prepare it, dissolve 0.26662 g of SrCl₂6H₂O in 1 mL of embryo water. At the time of use, add 10 µL of concentrated storage solution to 990 µL of Ca²⁺-free CZB medium and use immediately.
3. Place the oocytes in the Ca²⁺-free CZB medium containing SrCl₂6H₂O for activation; each droplet has a volume of 20 µL, and 20 oocytes are placed each time. Incubate for 20 min.
4. Simultaneously, establish a group for parthenogenesis activation without injecting round spermatids or spermatozoa. It should be noted that the parthenogenesis activation group is shown without statistical analysis, and the control group is ICSI.

7. Embryo transfer

1. House the ligated ICR male and female mice in a ratio of 1:2. The following morning, examine the female mice for the presence of a vaginal plug and select those with a vaginal plug for transplantation.
2. Inject the transferred embryos consisting of 2-cell embryos the previous morning and transfer them the next afternoon.
3. Make an incision on the back of the female mouse, expose the white fat and ovaries, and locate the enlarged part of the fallopian tube under an upright microscope (10x).
4. Use a 1 mL syringe to create an opening in the enlarged part of the fallopian tube and aspirate the embryos through an oral pipette. Gently introduce the embryos in the direction of the uterus. Suture the wound, using 4 x 10 models of curved needles with thread, with a thickness of 5-0 (0.09-0.11 mm). The suture is made in two layers, with one layer for the peritoneum and one layer for the outer skin.
5. For surrogate mice, perform cesarean sections based on the experimental schedule. Euthanize the mice by the cervical dislocation method, disinfect with alcohol, and open the abdominal cavity. Gently and quickly cut open the uterus and open the amniotic cavity to show the fetus and placenta. Remove the umbilical cord and cut from the side close to the fetus; the fetus was fed by the same period of breastfeeding mice.

8. Statistical analysis

1. Use GraphPad Prism 5 to analyze. Data are expressed in mean ± SD; P < 0.05 indicates a statistical difference, and P < 0.01 indicates a significant statistical difference.

Results

We initiated our investigation by examining AOA's effect on embryos' developmental capability. A schematic illustration of the experimental design is shown in Figure 1A. Before the spermatozoon injection, the oocytes underwent either AOA (A-ICSI) or remained untreated (ICSI). Detailed data on embryonic development is presented in Table 1. The results revealed no significant differences in cleavage, blastocyst, or birth rates between the A-ICSI and ICSI groups (P<...

Discussion

Assisted oocyte activation
A critical prerequisite for ROSI is AOA since round spermatids alone cannot initiate oocyte activation. Currently, the most established method in mice involves the use of strontium chloride^23,24, while the most advanced human application employs electrical activation^13,14. The timing of oocyte activation is also of great significance. As reported in the li...

Materials

Name	Company	Catalog Number	Comments
CaCl22H2O	Sigma	C7902	Preparation of CZB
Glucose	Sigma	G6152	Preparation of CZB
HEPES-Na (basic)	Sigma	H3784	Preparation of CZB
Hoechst 33342	Beyotime	C1025	FACS
human chorionic gonadotropin (HCG)	Ningbo Second Hormone Company	HCG	Ovulation promoting drugs
Hyaluronidase	Sigma	H3506	Removing granulosa cells around the oocyte
KCl	Sigma	P5405	Preparation of CZB
KH2PO4	Sigma	P5655	Preparation of CZB
KSOMaa	Caisson Labs	IVL04-100ML	Potassium simplex optimized medium supplemented with amino acids
L-glutamine	Sigma	G8540	Preparation of CZB
M2	Sigma	M7167-50ML	Operating fluid
MgSO47H2O	Sigma	M1880	Preparation of CZB
Na2-EDTA2H2O	Sigma	E5134	Preparation of CZB
NaCl	Sigma	S5886	Preparation of CZB
NaHCO3	Sigma	S5761	Preparation of CZB
Na-lactate 60% syrup d = 1.32 g/L	Sigma	L7900	Preparation of CZB
Na-pyruvate	Sigma	P4562	Preparation of CZB
Piezo drill tips (ICSI)	Eppendorf	piezoXpert	Piezoelectric membrane rupture
pregnant mare serum gonadotropin (PMSG)	Ningbo Second Hormone Company	PMSG	Ovulation promoting drugs
PVA	Sigma	P8136	Preparation of CZB